{"id":1090,"date":"2024-11-19T18:47:48","date_gmt":"2024-11-20T01:47:48","guid":{"rendered":"https:\/\/www.chem.ualberta.ca\/~clive\/?page_id=1090"},"modified":"2026-04-24T17:41:39","modified_gmt":"2026-04-24T23:41:39","slug":"publications-all","status":"publish","type":"page","link":"https:\/\/www.chem.ualberta.ca\/~clive\/publications-all\/","title":{"rendered":"Publications"},"content":{"rendered":"\t\t
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  1. <\/a>Chemistry of Tetracyclines, Clive, D.L.J. Quart Rev.<\/em> (London)<\/em> 1968<\/strong>, 22<\/i>, 435-456 (DOI<\/a>).<\/li>\n \t
  2. A New Method for Conversion of Aldoximes into Nitriles: Use of Chlorothionoformates, Clive, D.L.J. J. Chem. Soc., Chem. Comm<\/em>. 1970<\/strong>, 1014-1015 (DOI<\/a>).<\/li>\n \t
  3. Oxidation of Alkyl Carbazates: A New Method for Replacement of the Hydroxy-group by Halogen, Clive, D.L.J.; Denyer, C.V. J. Chem. Soc., Chem. Comm<\/em>.\u00a01971<\/strong>, 1112-1113 (DOI<\/a>).<\/li>\n \t
  4. Experiments on the Synthesis of Tetracycline. Part V. Photocyclisation of Ring B, Barton, D.H.R.; Clive, D.L.J.; Magnus, P.D.; Smith, G. J. Chem<\/em>. Soc. (C)<\/i>\u00a01971<\/strong>, 2193-2203 (DOI<\/a>).<\/li>\n \t
  5. Experiments on the Synthesis of Tetracycline. Part VI. Oxidation and Reduction of Potential Ring A Precursors, Barton, D.H.R.; Bould, L.; Clive, D.L.J.; Magnus, P.D.; Hase, T. J. Chem<\/em>. Soc.\u00a0(C)<\/i>\u00a01971<\/strong>, 2204-2215 (DOI<\/a>).<\/li>\n \t
  6. Desulphurization of Alkyl Chlorocarbonyl Disulphides – a Method for Replacement of -SH by -Cl, Clive, D.L.J.; Denyer, C.V. J. Chem. Soc., Chem. Comm<\/em>. 1972<\/strong>, 773-774 (DOI<\/a>).<\/li>\n \t
  7. New Method for Converting Epoxides into Olefins: Use of Triphenylphosphine Selenide and Trifluoroacetic Acid, Clive, D.L.J.; Denyer, C.V. J. Chem. Soc., Chem. Comm<\/em>. 1973<\/strong>, 253 (DOI<\/a>).<\/li>\n \t
  8. Fragmentation of Selenoxides: a New Method for Dehydrogenation of Ketones, Clive, D.L.J. J. Chem. Soc., Chem. Comm<\/em>. 1973<\/strong>, 695-696 (DOI<\/a>).<\/li>\n \t
  9. Reaction of Olefins with Benzeneselenenyl Bromide and Silver Trifluoroacetate: a New Method for Access to the Selenoxide Fragmentation Reaction, Clive, D.L.J. J. Chem. Soc., Chem. Comm<\/em>. 1974<\/strong>, 100 (DOI<\/a>).<\/li>\n \t
  10. Polyamide Supports for Polypeptide Synthesis, Atherton, E.; Clive, D.L.J.; Sheppard, R.C. J. Am. Chem. Soc<\/em>. 1975<\/strong>, 97<\/i>, 6584-6585 (DOI<\/a>).<\/li>\n \t
  11. Synthesis of Some Polypeptides on Polyamide Supports, Atherton, E.; Clive, D.L.J.; East, D.A.; Sheppard, R.C. Peptides 1976<\/strong>, Proceedings of the Fourteenth European Peptide Symposium, W\u00e9pion, Belgium, April 11-171976, pp. 291-297.<\/li>\n \t
  12. New Route to Bicyclic Lactones: Use of Benzeneselenenyl Chloride, Clive, D.L.J.; Chittattu, G. J. Chem. Soc., Chem. Comm<\/em>. 1977<\/strong>, 484-485 (DOI<\/a>).<\/li>\n \t
  13. A new route to ring-fused tetrahydrofurans: reactions of \u22064<\/sup>-unsaturated alcohols with phenylselenenyl chloride, Clive, D.L.J.; Chittattu, G.; Wong, C.K. Can. J<\/i>. Chem<\/em>. 1977<\/strong>, 55<\/i>, 3894-3897 (DOI<\/a>).<\/li>\n \t
  14. New Method for Deoxygenation of Sulphoxides: Use of O,O<\/i>-Diethyl Hydrogenphosphoroselenoate, Clive, D.L.J.; Kiel, W.A.; Menchen, S.M.; Wong, C.K. J. Chem. Soc., Chem. Comm<\/em>. 1977<\/strong>, 657-658 (DOI<\/a>).<\/li>\n \t
  15. New and Selective Method for Deoxygenating Epoxides: Use of the Organic Tellurium Reagent Sodium\u00a0O,O<\/i>-Diethyl Phosphorotelluroate, Clive, D.L.J.; Menchen, S.M.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Comm<\/em>. 1977<\/strong>, 658-659 (DOI<\/a>).<\/li>\n \t
  16. Cyclofunctionalisation of ortho<\/i>-Alkenyl Phenols: a New Method for Introducing the Benzeneseleno-group, Clive, D.L.J.; Chittattu, G.; Curtis, N.J.; Kiel, W.A.; Wong, C.K. J. Chem. Soc., Chem. Comm<\/em>. 1977<\/strong>, 725-727 (DOI<\/a>).<\/li>\n \t
  17. New Method for Reduction of Ketones and Primary Alcohols to Hydrocarbons: Reaction of the Derived Selenides with Tin Hydrides, Clive, D.L.J.; Chittattu, G.; Wong, C.K.\u00a0J<\/i>.\u00a0<\/em>Chem. Soc., Chem. Comm<\/em>. 1978<\/strong>, 41-42 (DOI<\/a>).<\/li>\n \t
  18. Cyclofunctionalisation of Olefinic Urethanes with Benzeneselenenyl Reagents: a New General Synthesis of Nitrogen Heterocycles, Clive, D.L.J.; Wong, C.K.; Kiel, W.A.; Menchen, S.M. J<\/i>. Chem. Soc., Chem. Comm<\/em>. 1978<\/strong>, 379-380 (DOI<\/a>).<\/li>\n \t
  19. New Method of Access to Selenoacetal Chemistry: Use of Tris(Phenylseleno)borane, Clive, D.L.J.; Menchen, S.M. J. Chem. Soc., Chem. Comm<\/em>. 1978<\/strong>, 356 (DOI<\/a>).<\/li>\n \t
  20. A New Use of Cyclofunctionalisation with Selenenyl Reagents: An Example of Carbon-Carbon Bond Formation, Clive, D.L.J.; Chittattu, G.; Wong, C.K. J. Chem. Soc., Chem. Comm<\/em>. 1978<\/strong>, 441-442 (DOI<\/a>).<\/li>\n \t
  21. Modern Organoselenium Chemistry, Clive, D.L.J. Tetrahedron<\/em> 1978<\/strong>, 34<\/i>, 1049-1132 (DOI<\/a>).<\/li>\n \t
  22. Selenium Reagents for Organic Synthesis, Clive, D.L.J. Aldrichimica Acta<\/em> 1978<\/strong>, 11<\/i>, 43-49.<\/li>\n \t
  23. 1,3-Transposition of Primary Allylic Alcohols: a New Application of Selenoxide Chemistry, Clive, D.L.J.; Chittattu, G.; Curtis, N.J.; Menchen, S.M. J. Chem. Soc., Chem. Comm<\/em>. 1978<\/strong>, 770-771 (DOI<\/a>).<\/li>\n \t
  24. New Reagents for Deoxygenation of Sulphoxides: Use of Compounds with Selenium-Boron Bonds, Clive, D.L.J.; Menchen, S.M. J. Chem. Soc., Chem. Comm<\/em>. 1979<\/strong>, 168-169 (DOI<\/a>).<\/li>\n \t
  25. New Route to Selenoacetals: Exchange Reaction between Acetals and Tris(phenylseleno)borane, Clive, D.L.J.; Menchen, S.M. J. Org. Chem<\/em>. 1979<\/strong>, 44<\/i>, 1883-1885 (DOI<\/a>).<\/li>\n \t
  26. Conversion of Aldehydes and Ketones into Selenoacetals: Use of Tris(phenylseleno)borane and Tris(methylseleno)borane, Clive, D.L.J.; Menchen, S.M. J. Org. Chem<\/em>. 1979<\/strong>, 44<\/i>, 4279-4285 (DOI<\/a>).<\/li>\n \t
  27. <\/a>Selenium and Tellurium Reagents for Organic Synthesis, Clive, D.L.J.; Plenary Lecture. Proceedings of the Third International Symposium on Organic Selenium and Tellurium Compounds. Metz, France, 9-12 July, 1979, Cagniant, D.; Kirsch, G., Eds.; Universite de Metz 1980<\/strong>, pp. 43-68.<\/li>\n \t
  28. Cyclofunctionalisation of Unsaturated Acids with Benzeneselenenyl Chloride. Kinetic and Thermodynamic Aspects of the Rules for Ring Closure, Clive, D.L.J.; Russell, C.G.; Chittattu, G.; Singh, A. Tetrahedron<\/em> 1980<\/strong>, 36<\/i>, 1399-1408 (DOI<\/a>).<\/li>\n \t
  29. Organic Tellurium and Selenium Chemistry. Reduction of Tellurides, Selenides, and Selenoacetals with Triphenyltin Hydride, Clive, D.L.J.; Chittattu, G.J.; Farina, V.; Kiel, W.A.; Menchen, S.M.; Russell, C.G.; Singh, A.; Wong, C.K.; Curtis, N.J. J. Am. Chem. Soc<\/em>. 1980<\/strong>, 102<\/i>, 4438-4447 (DOI<\/a>).<\/li>\n \t
  30. Cyclofunctionalisation of Olefinic Urethanes Using Benzeneselenenyl Chloride in the Presence of Silica Gel: A General Route to Nitrogen Heterocycles, Clive, D.L.J.; Farina, V.; Singh, A.; Wong, C.K.; Kiel, W.A.; Menchen, S.M. J. Org. Chem<\/em>. 1980<\/strong>, 45<\/i>, 2120-2126 (DOI<\/a>).<\/li>\n \t
  31. Alkali Metal O,O<\/i>-Diethyl Phosphorotelluroates, a Reagent Class for Deoxygenation of Epoxides, Especially Terminal Epoxides, Clive, D.L.J.; Menchen, S.M. J. Org. Chem<\/em>. 1980<\/strong>, 45<\/i>, 2347-2354 (DOI<\/a>).<\/li>\n \t
  32. Generation of Carbon-Carbon Double Bonds from \u03b2-Oxygenated Phenylseleno, Phenylthio, and lodo Species. A New Use for the Chlorotrimethylsilane-Sodium Iodide Reagent, Clive, D.L.J.; Kal\u00e8, V.N. J. Org. Chem<\/em>. 1981<\/strong>, 46<\/i>, 231-234 (DOI<\/a>).<\/li>\n \t
  33. Ylides and Carbanionic Compounds of Selenium and Tellurium, Clive, D.L.J. Organic Compounds of Sulphur, Selenium, and Tellurium, Vol. 6, Specialist Periodical Reports, Royal Society of Chemistry, London 1981<\/strong>, pp. 112-126.<\/li>\n \t
  34. New Method for Preparing \u03b2,\u03b3-Unsaturated Ketones: Use of Phenylselenoacetaldehyde, Clive, D.L.J.; Russell, C.G. J. Chem. Soc., Chem. Comm<\/em>. 1981<\/strong>, 434-436 (DOI<\/a>).<\/li>\n \t
  35. Peptide synthesis. Part 1. Preparation and use of polar supports based on poly(dimethylacrylamide), Arshady, R.; Atherton, E.; Clive, D.L.J.; Sheppard, R.C. J. Chem. Soc., Perkin Trans<\/em>. 1<\/i> 1981<\/strong>, 529-537 (DOI<\/a>).<\/li>\n \t
  36. Conjugate Addition of Methyl Groups to \u03b1,\u03b2-Unsaturated Aldehydes: Use of Me5<\/sub>Cu3<\/sub>Li2<\/sub>, Clive, D.L.J.; Farina, V.; Beaulieu, P.L. J. Chem. Soc., Chem. Comm<\/em>. 1981<\/strong>, 643-644 (DOI<\/a>).<\/li>\n \t
  37. Dehalogenation of \u03b1-Chloro and \u03b1-Bromo Ketones. Use of Sodium O,O<\/em>-Diethyl Phosphorotelluroate, Clive, D.L.J.; Beaulieu, P.L. J. Org. Chem<\/em>. 1982<\/strong>, 47<\/i>, 1124-1126 (DOI<\/a>).<\/li>\n \t
  38. \u03b1\u00a0Vinylation of Ketones. A General Method Using (Phenylseleno)acetaldehyde, Clive, D.L.J.; Russell, C.G.; Suri, S.C. J. Org. Chem<\/em>. 1982<\/strong>, 47<\/i>, 1632-1641 (DOI<\/a>).<\/li>\n \t
  39. New Method for Coupling Allylic Halides: Use of Te2\u2013<\/sup> Species, Clive, D.L.J.; Anderson, P.C.; Moss, N.; Singh, A. J. Org. Chem<\/em>. 1982<\/strong>, 47<\/i>, 1641-1647 (DOI<\/a>).<\/li>\n \t
  40. Me5<\/sub>Cu3<\/sub>Li2<\/sub>: A Reagent for Conjugate Methylation of \u03b1,\u03b2-Unsaturated Aldehydes, Clive, D.L.J.; Farina, V.; Beaulieu, P.L. J. Org. Chem<\/em>. 1982<\/strong>, 47<\/i>, 2752-2582 (DOI<\/a>).<\/li>\n \t
  41. Repetitive Ring Expansion of Cyclic Ketones by a Method Allowing Regiochemical Control, Clive, D.L.J.; Angoh, A.G.; Suri, S.C.; Rao, S.N.; Russell, C.G. J. Chem. Soc., Chem. Commun<\/em>. 1982<\/strong>, 828-830 (DOI<\/a>).<\/li>\n \t
  42. Formation of Carbon-Carbon Bonds by Ring Closure of \u03b2-Phenylselenocrotonates, Clive, D.L.J.; Beaulieu, P.L. J. Chem. Soc., Chem. Commun<\/em>. 1983<\/strong>, 307-309 (DOI<\/a>).<\/li>\n \t
  43. Sapphyrins: Novel Aromatic Pentapyrrolic Macrocycles, Bauer, V.J.; Clive, D.L.J.; Dolphin, D.; Paine, J.B., Ill; Harris, F.L.; King, M.M.; Loder, J.; Wang, S.-W.C.; Woodward, R.B. J. Am. Chem<\/em>. Soc.1983<\/strong>, 105<\/i>, 6429-6436 (DOI<\/a>).<\/li>\n \t
  44. Synthetic Studies Related to Compactin and Mevinolin: a New Synthesis of the Hexahydronaphthalene Portion of Compactin, Anderson, P.C.; Clive, D.L.J.; Evans, C.F. Tetrahedron Lett.<\/em> 1983<\/strong>, 24<\/i>, 1373-1376 (DOI<\/a>).<\/li>\n \t
  45. Synthesis of Ketones by Cyclization of Cyano and Acetylenic Radicals: Use of \u03b4-Hydroxy Nitriles and \u03b4- or \u03b5-Hydroxy Acetylenes, Clive, D.L.J.; Beaulieu, P.L.; Set, L. J.\u00a0<\/em>Org. Chem<\/em>.1984<\/strong>, 49<\/em>, 1313-1314 (DOI<\/a>).<\/li>\n \t
  46. Studies Related to Thromboxane A2<\/sub>: A Formal Synthesis of Optically Active 9\u03b1,11\u03b1-Thiathromboxane A2<\/sub> Methyl Ester from Levoglucosan, Kal\u00e8, V.N.; Clive, D.L.J.\u00a0J.\u00a0<\/em><\/em>Org. Chem<\/em>. 1984<\/strong>, 49<\/i>, 1554-1563 (DOI<\/a>).<\/li>\n \t
  47. A Synthetic Equivalent for the Butadienyl Carbonium Ion: Use of 4-(Trimethylsilyl)but-2-ynal for Preparation of 1,3-Dienes and Macroexpansion of Cyclic Ketones, Angoh, A.G.; Clive, D.L.J. J. Chem. Soc., Chem. Commun<\/em>. 1984<\/strong>, 534-536 (DOI<\/a>).<\/li>\n \t
  48. Synthetic Studies Related to Compactin and Mevinolin: A New Synthesis of the Lactone System, Majewski, M.; Clive, D.L.J.; Anderson, P.C. Tetrahedron Lett<\/em>. 1984<\/strong>, 25<\/i>, 2101-2104 (DOI<\/a>).<\/li>\n \t
  49. 2-(Phenylseleno)prop-2-enenitrile: a Three-carbon Unit for Radical Cyclization, Angoh, A.G.; Clive, D.L.J. J<\/i>. Chem. Soc., Chem. Commun<\/em>. 1985<\/strong>, 941-942 (DOI<\/a>).<\/li>\n \t
  50. Radical Annulation: A Method for Preparation of Carbocycles, Angoh, A.G.; Clive, D.L.J. J. Chem. Soc., Chem. Commun<\/em>. 1985<\/strong>, 980-982 (DOI<\/a>).<\/li>\n \t
  51. Synthesis of Spiro-Compounds: Use of Diselenoacetals for Generation of Quaternary Centres by Alkylation and Radical Cyclization, Set, L.; Cheshire, D.R.; Clive, D.L.J. Chem. Soc.,\u00a0J.\u00a0<\/em>Chem. Commun<\/em>. 1985<\/strong>, 1205-1207 (DOI<\/a>).<\/li>\n \t
  52. Synthetic Studies Related to Compactin: Use of Tri-O<\/i>-acetyl-d<\/span>-glucal for Preparation of Chiral Cyclohexenes, Prasad, J.S.; Clive, D.L.J.; da Silva, G.V.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1986<\/strong>, 51<\/i>, 2717-2721 (DOI<\/a>).<\/li>\n \t
  53. A New Method for Synthesis of Five-membered Carbocycles: Use of the Ester Enolate Rearrangement in Conjunction with Radical Cyclization, Mohammed, A.Y.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1986<\/strong>, 588-589 (DOI<\/a>).<\/li>\n \t
  54. Synthesis of Spiro-compounds Related to Fredericamycin A, Bennett, S.M.; Clive, D.L.J. J<\/i>. Chem. Soc., Chem. Commun<\/em>. 1986<\/strong>, 878-880 (DOI<\/a>).<\/li>\n \t
  55. Synthesis of Heterocyclic Compounds Related to Fredericamycin A – the Cyclopent[g]isoquinoline System, Clive, D.L.J.; Sedgeworth, J.\u00a0J.\u00a0<\/em>Heterocyclic Chem<\/em>. 1987<\/strong>, 24<\/i>, 509-511 (DOI<\/a>).<\/li>\n \t
  56. Radical Spirocyclization: Synthesis of an Appropriately Oxygenated Spiro Compound Related to the Antitumor Antibiotic Fredericamycin A, Clive, D.L.J.; Angoh, A.G.; Bennett, S.M.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1987<\/strong>, 52<\/i>, 1339-1342 (DOI<\/a>).<\/li>\n \t
  57. Rules for Ring Fusion Geometry and the Preparation of trans<\/i>– or cis<\/i>-Fused Bicyclic Compounds by Radical Closure, Clive, D.L.J.; Cheshire, D.R.; Set, L.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1987<\/strong>, 353-355 (DOI<\/a>).<\/li>\n \t
  58. Construction of Five-Membered Rings by Michael Addition\u2013Radical Cyclization, Clive, D.L.J.; Boivin, T.L.B.; Angoh, A.G.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1987<\/strong>, 52<\/i>, 4943-4953 (DOI<\/a>).<\/li>\n \t
  59. On Baldwin’s Kinetic Barrier Against 5-(Enol-endo<\/i>)-exo<\/i>-trigonal Closures: a Comparison of Ionic and Analogous Radical Reactions, and a New Synthesis of Cyclopentanones, Clive, D.L.J.; Cheshire, D.R. J<\/i>. Chem. Soc., Chem. Commun<\/em>. 1987<\/strong>, 1520-1523 (DOI<\/a>).<\/li>\n \t
  60. Total Synthesis of Both (+)-Compactin and (+)-Mevinolin. A General Strategy Based on the Use of a Special TiCl3<\/sub>\/C8<\/sub>K Mixture for Dicarbonyl Coupling, Clive, D.L.J.; Keshava Murthy, K.S.; Wee, A.G.H.; Prasad, J.S.; da Silva, G.V.J.; Majewski, M.; Anderson, P.C.; Haugen, R.C.; Heerze, L.D.\u00a0J.\u00a0<\/em>Am. Chem. Soc.<\/em> 1988<\/strong>, 110<\/i>, 6914-6916 (DOI<\/a>).<\/li>\n \t
  61. Synthetic methodology involving radical cyclization: spiro compounds and \u03b1-oxo radicals, Clive, D.L.J. Pure Appl. Chem<\/em>. 1988<\/strong>, 60<\/i>, 1645-1654 (DOI<\/a>).<\/li>\n \t
  62. Formation of Cis-Fused Cyclopentanoids by Michael Addition and Radical Cyclization, Clive, D.L.J.; Boivin, T.L.B.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1989<\/strong>, 54<\/i>, 1997-2003 (DOI<\/a>).<\/li>\n \t
  63. Synthetic Applications of Radical Ring-Opening: Use of Cyclopropylmethyl Radicals, Clive, D.L.J.; Daigneault, S.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1989<\/strong>, 332-335 (DOI<\/a>).<\/li>\n \t
  64. Conversion of Olefins into Five-membered Nitrogen Heterocycles by Radical Cyclization, Clive, D.L.J.; Mohammed, A.Y. Heterocycles<\/em> 1989<\/strong>, 28<\/i>, 1157-1167 (DOI<\/a>).<\/li>\n \t
  65. <\/a>Total Synthesis of Both (+)-Compactin and (+)-Mevinolin. A General Strategy Based on the Use of a Special Titanium Reagent for Dicarbonyl Coupling, Clive, D.L.J.; Keshava Murthy, K.S.; Wee, A.G.H.; Siva Prasad, J.; da Silva, G.V.J.; Majewski, M.; Anderson, P.C.; Evans, C.F.; Haugen, R.D.; Heerze, L.D.; Barrie, J.R. J. Am. Chem. Soc.\u00a0<\/i>1990<\/strong>, 112<\/i>, 3018-3028 (DOI<\/a>).<\/li>\n \t
  66. Synthesis of (\u00b1)-Frullanolide: An Application of Radical Closure, Clive, D.L.J.; Joussef, A.C.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1990<\/strong>, 55<\/i>, 1096-1098 (DOI<\/a>).<\/li>\n \t
  67. A Route to Linear, Bridged, or Spiro Polycyclic Compounds: Sequential Use of the Intermolecular Diels-Alder Reaction and Radical Cyclization, Clive, D.L.J.; Bergstra, R.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1990<\/strong>, 55<\/i>, 1786-1792 (DOI<\/a>).<\/li>\n \t
  68. Chemical Synthesis of 3-Ethylcompactin, an Inhibitor of 3-Hydroxy-3-methylglutarylcoenzyme A Reductase, Clive, D.L.J.; Keshava Murthy, K.S.; George, R.; Poznansky, M.J.\u00a0J.\u00a0<\/em>Chem. Soc., Perkin Trans<\/em>. 1<\/i> 1990<\/strong>, 2099-2108 (DOI<\/a>).<\/li>\n \t
  69. New Low-Valent Titanium Reagents for Dicarbonyl Coupling and their Use in a General Method of Annulation, Clive, D.L.J.; Keshava Murthy, K.S.; Zhang, C.; Hayward, W.D.; Daigneault, S. J<\/i>. Chem. Soc., Chem. Commun<\/em>. 1990<\/strong>, 509-511 (DOI<\/a>).<\/li>\n \t
  70. Construction of trans<\/i>-Ring-fused Compounds by Radical Cyclization, Clive, D.L.J.; Manning, H.W.; Boivin, T.L.B. J. Chem. Soc., Chem. Commun<\/em>. 1990<\/strong>, 972-974 (DOI<\/a>).<\/li>\n \t
  71. Regioselective Oxidation of Polyalkoxy Naphthalenes: Formation of Naphthoquinones by Ammonium Cerium(IV) Nitrate Oxidation of Methoxymethyl Ethers, Clive, D.L.J.; Middleton, D.S. Israel J. Chem<\/em>. 1991<\/strong>, 31<\/i>, 211-213 (DOI<\/a>).<\/li>\n \t
  72. Model Studies Related to the Synthesis of Fredericamycin A., Clive, D.L.J.; Khodabocus, A.; Vernon, P.G.; Angoh, A.G.; Bordeleau, L.; Middleton, D.S.; Lowe, C.; Kellner, D. J. Chem. Soc., Perkin Trans<\/em>. 1<\/i> 1991<\/strong>, 1433-1444 (DOI<\/a>). [See J. Chem. Soc., Perkin Trans<\/em>. 1\u00a0<\/em>1992<\/b>, 739 for correction of typographical error.]<\/li>\n \t
  73. Use of Radical Ring-Opening for Introduction of Alkyl and Substituted Alkyl Groups with Stereochemical Control: A Synthetic Application of Cyclopropylcarbinyl Radicals, Clive, D.L.J.; Daigneault, S.\u00a0 J. Org. Chem<\/em>. 1991<\/strong>, 56<\/i>, 3801-3814 (DOI<\/a>).<\/li>\n \t
  74. Short Synthesis of (\u00b1)-5-(3-Furyl)octahydro-8-methylindolizines, Alkaloids Related to a Component of Castoreum. Use of Radical Cyclization, Clive, D.L.J.; Bergstra, R.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1991<\/strong>, 56<\/i>, 4976-4977 (DOI<\/a>).<\/li>\n \t
  75. Sequential Radical Ring Closure-Radical Ring Opening: Use in the Preparation of Benzofurans, Clive, D.L.J.; Daigneault, S.\u00a0J. Org. Chem<\/em>. 1991<\/strong>, 56<\/i>, 5285-5289 (DOI<\/a>).<\/li>\n \t
  76. A Free Radical Method for Attaching an Oxygen-containing Ring to Either Face of a Bicyclic Structure, Clive, D.L.J.; Joussef, A.C.\u00a0J.\u00a0<\/em>Chem. Soc., Perkin Trans<\/em>. 1<\/i> 1991<\/strong>, 2797-2799 (DOI<\/a>).<\/li>\n \t
  77. New Low-Valent Titanium Reagents for Dicarbonyl Coupling and Their Use in a General Method of Annulation, Clive, D.L.J.; Zhang, C.; Keshava Murthy, K.S.; Hayward, W.D.; Daigneault, J. Org. Chem<\/em>. 1991<\/strong>, 56<\/i>, 6447-6458 (DOI<\/a>). (See J. Org. Chem<\/i>. 1993<\/strong>, 58<\/i>, 3472 for correction of typographical error.)<\/li>\n \t
  78. Radical Cyclizations of Geminal Radical Precursors, Clive, D.L.J.; Cole, D.C.\u00a0J.\u00a0<\/em>Chem. Soc., Perkin Trans<\/em>. 1<\/i>\u00a01991<\/strong>, 3263-3270 (DOI<\/a>).<\/li>\n \t
  79. A New Method for Silylation of Hydroxylic Compounds: Reaction of Phenols and Alcohols with Silanols Mediated By Diethyl Azodicarboxylate and Triphenylphosphine, Clive, D.L.J.; Kellner, D. Tetrahedron Lett<\/em>. 1991<\/strong>,<\/b>\u00a032<\/i>, 7159-7160 (DOI<\/a>).<\/li>\n \t
  80. Protecting Group Improvement by Isotopic Substitution: Application to the Synthesis of the Quinone System of Fredericamycin A, Clive, D.L.J.; Khodabocus, A.; Cantin, M.; Tao, Y.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1991<\/strong>, 1755-1757 (DOI<\/a>).<\/li>\n \t
  81. Total Synthesis of (+)-Mevinolin and (+)-Compactin, Clive, D.L.J.; Keshava Murthy, K.S.; Wee, A.G.H.; Siva Prasad, J.; da Silva, G.V.J.; Majewski, M.; Anderson, P.C. “Studies in Natural Products Chemistry”, Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 1992<\/strong>; Vol. 11, 335-377.<\/li>\n \t
  82. Total Synthesis of Crystalline (\u00b1)-Fredericamycin A. Use of Radical Spirocyclization, Clive, D.L.J.; Tao, Y.; Khodabocus, A.; Wu, Y.-J.; Angoh, A.G.; Bennett, S.M.; Boddy, C.N.; Bordeleau, L.; Kellner, D.; Kleiner, G.; Middleton, D.S.; Nichols, C.J.; Richardson, S.R.; Vernon, P.G.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1992<\/strong>, 1489-1490 (DOI<\/a>).<\/li>\n \t
  83. Synthesis of Carbazomycin B, Clive, D.L.J.; Etkin, N.; Joseph, T.; Lown, J.W.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1993<\/strong>, 58<\/i>, 2442-2445 (DOI<\/a>).<\/li>\n \t
  84. trans<\/i> Ring-fused Bicyclic Structures by 6-exo<\/i>-Trigonal Radical Closure: Use of the Triethylborane-Stannane-Air System for lntramolecular Radical Addition to Aldehydes, Clive, D.L.J.; Postema, M.H.D.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1993<\/strong>, 429-430 (DOI<\/a>). [See J. Chem. Soc., Chem. Commun<\/em>. 1993<\/strong>, 1240 for correction of typographical error.)<\/li>\n \t
  85. Protecting Group Improvement by Isotopic Substitution: Synthesis of the Quinone System of Fredericamycin A, Clive, D.L.J.; Cantin, M.; Khodabocus, A.; Kong, X.; Tao, Y. Tetrahedron<\/em> 1993<\/strong>, 49<\/i>, 7917-7930 (DOI<\/a>).<\/li>\n \t
  86. Formal Preparation of Semisynthetic Analogues of the Cholesterol-lowering Agent Mevinolin, Clive, D.L.J.; Zhang, C.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1993<\/strong>, 647-649 (DOI<\/a>).<\/li>\n \t
  87. A General Method for Iterative Cyclopentannulation: Sequential Use of Claisen Rearrangement and Radical Enyne Closure, Clive, D.L.J.; Manning, H.W.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1993<\/strong>, 666-667 (DOI<\/a>).<\/li>\n \t
  88. Reaction of cis<\/i>-Vicinal Dimesylates with Te2\u2013<\/sup>: a Method for converting cis<\/i>-Vicinal Diols into Olefins and its Use in the Preparation of 2′,3′-Didehydro-2′,3′-dideoxynucleosides, Clive, D.L.J.; Wickens, P.L.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1993<\/strong>, 923-924 (DOI<\/a>).<\/li>\n \t
  89. Formation of trans<\/i> Ring-Fused Compounds by an Alkylation-Radical Cyclization Sequence, Clive, D.L.J.; Manning, H.W.; Boivin, T.L.B.; Postema, M.H.D.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1993<\/strong>, 58<\/i>, 6857-6873 (DOI<\/a>).<\/li>\n \t
  90. Ozonolysis of Olefinic Phenyl Selenides with Preservation of the Selenium Unit: A Route to Phenylseleno Aldehydes and Ketones, Clive, D.L.J.; Postema, M.H.D. Chem. Soc., Chem. Commun<\/em>. 1994<\/strong>, 235-236 (DOI<\/a>).<\/li>\n \t
  91. Formation of Angularly-Fused Triquinanes by Successive Use of the Pauson-Khand Reaction and Radical Closure, Clive, D.L.J.; Cole, D.C.; Tao, Y.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1994<\/strong>, 59<\/i>, 1396-1406 (DOI<\/a>).<\/li>\n \t
  92. Synthesis of \u03b1-Amino Acids by Addition of Putative Azido Radicals to \u03b1-Methoxy Acrylonitriles Derived From Aldehydes and Ketones, Clive, D.L.J.; Etkin. N. Tetrahedron Lett<\/em>. 1994<\/strong>, 35<\/i>, 2459-2462 (DOI<\/a>).<\/li>\n \t
  93. Total Synthesis of Crystalline (\u00b1)-Fredericamycin A. Use of Radical Spirocyclization, Clive, D.L.J.; Tao, Y.; Khodabocus, A.; Wu, Y.-J.; Angoh, A.G.; Bennett, S.M.; Boddy, C.N.; Bordeleau, L.; Kellner, D.; Kleiner, G.; Middleton, D.S.; Nichols, C.J.; Richardson, S.R.; Vernon, P.G. J. Am. Chem. Soc<\/em>. 1994<\/strong>, 116<\/i>, 11275-11286 (DOI<\/a>).\"\"<\/li>\n \t
  94. Addition of dimethylphenylsilyl cuprates to vinyl epoxides: Effect of cuprate stoichiometry on stereochemistry and regiochemistry, Clive, D.L.J.; Zhang, C.; Zhou, Y.; Tao, Y. J. <\/i>Organomet. Chem<\/em>. 1995<\/strong>, 489<\/i>, C35-C37 (DOI<\/a>).\"\"<\/li>\n \t
  95. Synthesis of the Sesquiterpene (\u00b1)-Ceratopicanol: Use of Radicals Derived from Epoxides, Clive, D.L.J.; Magnuson, S.R. Tetrahedron Lett<\/em>.\u00a01995<\/strong>, 36<\/i>, 15-18 (DOI<\/a>).\"\"<\/li>\n \t
  96. Studies on the Degradation of Mevinolin and Compactin: A Formal Route to Semisynthetic Analogues, Clive, D.L.J.; Zhang, C.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1995<\/strong>, 60<\/i>, 1413-1427 (DOI<\/a>).\"\"<\/li>\n \t
  97. 5-endo<\/i>-Trigonal Radical Cyclization – A General Procedure for Making Five-membered Rings, Clive, D.L.J.; Cantin, M.\u00a0J.\u00a0<\/em>Chem. Soc., Chem. Commun<\/em>. 1995<\/strong>, 319-320 (DOI<\/a>).\"\"<\/li>\n \t
  98. A Nitrogen-Containing Stannane for Free Radical Chemistry, Clive, D.L.J.; Yang, W.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1995<\/strong>, 60<\/i>, 2607-2609 (DOI<\/a>).\"\"<\/li>\n \t
  99. Total Synthesis of Crystalline (\u00b1)-Fredericamycin A, Clive, D.L.J.; Tao, Y.; Khodabocus, A.; Wu, Y.-J.; Angoh, A.G.; Bennett, S.M.; Boddy, C.N.; Bordeleau, L.; Cantin, M.; Cheshire, D.R.; Kellner, D.; Kleiner, G.; Middleton, D.S.; Nichols, C.J.; Richardson, S.R.; Set, L.; Vernon, P.G. “Studies in Natural Products Chemistry”, Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 1995<\/strong>; Vol. 16, 27-74 (DOI<\/a>).\"\"<\/li>\n \t
  100. Preparation of a Semisynthetic Analogue of Mevinolin and Compactin, Clive, D.L.J.; Wickens, P.L.; da Silva, G.V.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1995<\/strong>, 60<\/i>, 5532-5536 (DOI<\/a>).\"\"<\/li>\n \t
  101. Wittig chain extension of unprotected carbohydrates: formation of carbohydrate-derived \u03b1,\u03b2-unsaturated esters, Railton, C.J.; Clive, D.L.J. Carbohydr.<\/i> Res. <\/i>1996<\/b>, 281<\/i>, 69-77 (DOI<\/a>).\"\"<\/li>\n \t
  102. Cyclopentannulation by an Iterative Process of Sequential Claisen Rearrangement and Enyne Radical Closure: Routes to Triquinane and Propellane Systems and Use in the Synthesis of (\u00b1)-Ceratopicanol, Clive, D.L.J.; Magnuson, S.M.; Manning, H.M.; Mayhew, D.L.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 1996<\/strong>, 61<\/i>, 2095-2108 (DOI<\/a>).\"\"<\/li>\n \t
  103. Further Model Studies Related to Fredericamycin A: Analogues in which Ring C is Expanded to Six Atoms, and an Examination of the Diastereoselectivity of Radical Spirocyclization, Clive, D.L.J.; Kong, X.; Paul, C.C. Tetrahedron<\/em> 1996<\/strong>, 52<\/i>, 6085-6116 (DOI<\/a>).\"\"<\/li>\n \t
  104. Synthesis of (\u00b1)-Calicheamicinone by Two Related Methods, Clive, D.L.J.; Bo, Y.; Tao. Y.; Daigneault, S.; Wu, Y.-J.; Meignan, G.\u00a0J.\u00a0<\/em>Am. Chem. Soc<\/em>. 1996<\/strong>, 118<\/i>, 4904-4905 (DOI<\/a>).\"\"<\/li>\n \t
  105. Synthesis of crystalline (\u00b1)-A58365B – an inhibitor of angiotensin-converting enzyme, Clive, D.L.J.; Zhou, Y.; de Lima, D.P. Chem. Commun.<\/i> 1996<\/strong>, 1463-1464 (DOI<\/a>).\"\"<\/li>\n \t
  106. Preparation of tetrahydrofuran, \u03b3-lactone, chromanol, and pyrrolidine systems by sequential 5-exo<\/i>-digonal radical cyclization, 1,5- hydrogen transfer from silicon, and 5-endo<\/i>-trigonal cyclization, Clive, D.L.J.; Yang, W. Chem Commun<\/em>. 1996<\/strong>, 1605-1606 (DOI<\/a>).\"\"<\/li>\n \t
  107. Synthesis of 2′,3′-Didehydro-2’3′-dideoxynucleosides by Reaction of 5′-Protected Nucleoside 2′,3′-Dimesylates with Telluride Dianion: A General Route from Cis<\/i> Vicinal Diols to Olefins, Clive, D.L.J.; Wickens, P.L.; Sgarbi, P.W.M. J.\u00a0<\/i>Org. Chem<\/em>. 1996<\/strong>, 61<\/i>, 7426-7437 (DOI<\/a>).\"\"<\/li>\n \t
  108. Formal synthesis of (\u2013)-calicheamicinone and of (+)-calicheamicinone, Clive, D.L.J.; Selvakumar, N.\u00a0Chem. Commun<\/em>.\u00a01996<\/strong>, 2543-2544 (DOI<\/a>).\"\"<\/li>\n \t
  109. Synthesis of the aromatic unit of calicheamicin Hu, Y.-Z.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Chem. Soc., Perkin Trans<\/em>. 1\u00a0<\/em>1996<\/b>,\u00a0<\/b>1421-1424 (DOI<\/a>).\"\"<\/li>\n \t
  110. Prepaparation of \u03b1-(2,2-diphenylhydrazino)- and \u03b1-(benzyloxyamino)lactones by radical cyclization: use of glyoxylic acid diphenylhydrazone and glyoxylic acid O<\/em>-benzyloxime, Clive, D.L.J.; Zhang, Chem. Commun<\/em>. 1997<\/strong>, 549-550 (DOI<\/a>).\"\"<\/li>\n \t
  111. Synthesis of 2′,3′-Didehydro-2′,3′-dideoxynucleosides by Reaction of 5′-O<\/em>-Protected Nucleoside 2′,3′-Dimesylates with Lithium Arylselenolates, Clive, D.L.J.; Sgarbi, P.W.M., Wickens, P.L. J.\u00a0<\/i>Org. Chem. <\/em>1997<\/strong>, 62<\/i>, 3751-3753 (DOI<\/a>).\"\"<\/li>\n \t
  112. Radical Allylations with Trimethyl[2-[(tributylstannyl)methyl]-2-propenyl]silane or Trimethyl [2-[(triphenylstannyl)methyl]-2-propenyl]silane, Clive, D.L.J.; Paul, C.C.; Wang, Z.\u00a0J.\u00a0<\/em>Org. Chem<\/em>.1997<\/strong>, 62<\/i>, 7028-7032 (DOI<\/a>).\"\"<\/li>\n \t
  113. Synthesis of the carbobicyclic substructure of CP-225,917 and CP-263,114, Sgarbi, P.W.M.; Clive, D.L.J. Chem Commun<\/em>. 1997<\/strong>, 2157-2158 (DOI<\/a>).\"\"<\/li>\n \t
  114. Synthesis of the Angiotensin-Converting Enzyme Inhibitor (\u00b1)-A58365A, Clive, D.L.J.; Coltart, D.M. Tetrahedron Lett<\/em>. 1998<\/strong>, 39<\/i>, 2519-2522 (DOI<\/a>).\"\"<\/li>\n \t
  115. A synthetic route from D-glucose to D-myo<\/em>-inositol-1,4,5-tris(dihydrogenphosphate): use of an unusual ene reaction and the Bu2<\/sub>SnCl2<\/sub>\/Bu2<\/sub>SnH2<\/sub> reagent, Clive, D.L.J.; Xiao H.; Postema, M.H.D.; Mashimbye, M.J. Tetrahedron<\/em> Lett<\/em>.\u00a01998<\/strong>, 39<\/i>, 4231-4234 (DOI<\/a>).\"\"<\/li>\n \t
  116. Formal Synthesis of Natural Epibatidine and of its Enantiomer: Use of Radical Cyclization in an Enantiospecific Route, Clive, D.L.J.; Yeh, V.S.C. Tetrahedron<\/em> Lett<\/em>. 1998<\/strong>, 39<\/i>, 4789-4792 (DOI<\/a>).\"\"<\/li>\n \t
  117. Synthesis of (\u00b1)-Calicheamicinone by Two Methods, Clive, D.L.J.; Bo, Y.; Tao, Y.; Daigneault, S.; Wu, Y.-J.; Meignan, G.\u00a0J.\u00a0<\/em>Am. Chem. Soc<\/em>. 1998<\/strong>, 120<\/i>, 10332-10349 (DOI<\/a>).\"\"<\/li>\n \t
  118. Synthesis of C<\/em>-Glycosyl Lactones and Protected C<\/em>-Glycosyl Amino Acids: Use of Radical Cyclization, Zhang, J.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>.1999<\/strong>, 64<\/i>, 770-779 (DOI<\/a>).\"\"<\/li>\n \t
  119. Synthesis and X-Ray Crystal Structure of (\u2013)-Calicheamicinone, Clive, D.L.J.; Bo, Y.; Selvakumar, N.; McDonald, R.; Santarsiero, B.D. Tetrahedron<\/em> 1999<\/strong>, 55<\/i>, 3277-3290 (DOI<\/a>).\"\"<\/li>\n \t
  120. Synthesis of the Angiotensin-Converting Enzyme Inhibitors (\u2013)-A58365A and (\u2013)-A58365B from a Common Intermediate, Clive, D.L.J.; Coltart, D.M.; Zhou, Y. J.\u00a0<\/em>Org. Chem<\/em>. 1999<\/strong>, 64<\/i>, 1447-1454 (DOI<\/a>).\"\"<\/li>\n \t
  121. Synthesis of (+)-Furanomycin: Use of Radical Cyclization, Clive, D.L.J.; Zhang, J.\u00a0J.\u00a0<\/em>Org. Chem. <\/em>1999<\/strong>, 64<\/i>, 1754-1757 (DOI<\/a>).\"\"<\/li>\n \t
  122. Applications of 5-Endo<\/i>-trigonal Cyclization: Construction of Compounds Relevant to the Synthesis of Prostaglandins and Methyl epi-<\/em>Jasmonate, Sannigrahi, M.; Mayhew, D.L.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem.<\/em> 1999<\/strong>, 64<\/i>, 2776-2788 (DOI<\/a>).\"\"<\/li>\n \t
  123. Formal Synthesis of D-myo<\/i>-lnositol-1,4,5-Tris(dihydrogen phosphate): Cyclization by an Unusual Ene Reaction and Use of the Bu2<\/sub>SnCl2<\/sub>\/Bu\u00a02<\/span>SnH2<\/span>\u00a0Reagent for Generating an Equatorial Alcohol, Clive, D.L.J.; He, X.; Postema, M.H.D.; Mashimbye, M.J.\u00a0J.\u00a0<\/em>Org. Chem.<\/em> 1999<\/strong>, 64<\/i>, 4397-4410 (DOI<\/a>).\"\"<\/li>\n \t
  124. Studies on the Preparation of 3,4-Disubstituted 2-Methoxypyridines, Pelisson, M.M.M.; da Silva, G.V.J.; Clive, D.L.J.; Coltart, D.M.; Hof, F.A.\u00a0J.\u00a0<\/em>Heterocyclic Chem<\/em>. 1999<\/strong>, 36<\/i>, 653-658 (DOI<\/a>).\"\"<\/li>\n \t
  125. Synthesis of tricyclic bridgehead olefins related to the core structure of CP-225,917 and CP-263,114 – solvent, strain, and substitution effects on siloxy-Cope rearrangements, Clive, D.L.J.; Sun, S.; He, X.; Zhang, J.; Gagliardini, V. Tetrahedron Lett<\/em>. 1999<\/strong>, 40<\/i>, 4605-4609 (DOI<\/a>).\"\"<\/li>\n \t
  126. Model Studies Related to CP-225,917: Stereocontrolled Generation of the Quaternary Center, Clive, D.L.J.; Zhang, J. Tetrahedron Lett.<\/em> 1999<\/strong>, 41<\/i>, 12059-12068 (DOI<\/a>).\"\"<\/li>\n \t
  127. Synthesis of racemic brevioxime, Clive, D.L.J.; Hisaindee, S. Chem. Commun<\/em>. 1999<\/strong>, 2251-2252 (DOI<\/a>).\"\"<\/li>\n \t
  128. Synthesis of a 6-azaspiro[4.5]decane related to Halichlorine and the pinnaic acids, Clive, D.L.J.; Yeh, V.S.C. Tetrahedron Lett<\/em>. 1999<\/strong>, 40<\/i>, 8503-8507 (DOI<\/a>).\"\"<\/li>\n \t
  129. <\/a>Radical cyclization of O<\/em>-trityl oximino esters\u2014a ring closure that preserves the oxime function, Clive, D.L.J.; Subedi, R. Chem. Commun<\/em>. 2000<\/strong>, 237-238 (DOI<\/a>).\"\"<\/li>\n \t
  130. Synthesis of biaryls by intramolecular radical transfer: use of phospinates, Clive, D.L.J.; Kang, S. Tetrahedron Lett<\/em>. 2000<\/strong>, 41<\/i>, 1315-1319 (DOI<\/a>).\"\"<\/li>\n \t
  131. Effect of Aryl Substituents on Rate of Desulfonylation of Aryl Alkyl Sulfones: Superiority of p<\/em>-Fluorophenyl- and 2-Naphthyl Sulfones, Clive, D.L.J.; Yeh, V.S.C. Synth. Commun<\/em>. 2000<\/strong>, 30<\/i>, 3267-3274 (DOI<\/a>).\"\"<\/li>\n \t
  132. Synthesis of Racemic Brevioxime and Related Model Compounds, Clive, D.L.J.; Hisaindee, S.\u00a0J.\u00a0<\/em>Org. Chem.<\/em> 2000<\/strong>, 65<\/i>, 4923-4929 (DOI<\/a>).\"\"<\/li>\n \t
  133. Synthetic studies on calicheamicin \u03b31<\/sub>I<\/sup> \u2014\u00a0Synthesis of (\u2013)-Calicheamicinone and models representing the four sugars and the aromatic system, Clive, D.L.J.; Tao, Y.; Bo, Y.; Hu, Y-Z.; Selvakumar, N.; Sun, S.; Daigneault, S.; Wu, Y.-J. Chem. Commun<\/em>. 2000<\/strong>, 1341-1350 (DOI<\/a>).\"\"<\/li>\n \t
  134. An approach to the anhydride unit of CP-225,917 and CP-263,114, Clive, D.L.J.; Sun, S.; Gagliardini, V.; Sano, M.K. Tetrahedron Lett<\/em>. 2000<\/strong>, 41<\/i>, 6259-6263 (DOI<\/a>).\"\"<\/li>\n \t
  135. Conversion of some substituted phenols to the corresponding masked thiophenols, synthesis of a dinickel(II) dithiolate macrocyclic complex and isolation of some metal- and ligand-based oxidation products, Brooker, S.; Caygill, G.B.; Croucher, P.D.; Davidson, T.C.; Clive, D.L.J.; Magnuson, S.M.; Cramer, S.P.; Ralston, C.Y. J. Chem. Soc., Dalton Trans.\u00a0<\/em>2000<\/strong>, 3113-3121 (DOI<\/a>).\"\"<\/li>\n \t
  136. Synthesis of (\u00b1)-Puraquinonic Acid \u2013 an Inducer of Cell Differentiation, Clive, D.L.J.; Sannigrahi, M.; Hisaindee, S.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2001<\/strong>, 66<\/i>, 954-961 (DOI<\/a>).\"\"<\/li>\n \t
  137. Preparation of \u03b1-(2,2-Diphenylhydrazino)lactones and Related Compounds by Radical Cyclization: Use of Glyoxylic Acid Hydrazone Derivatives, Clive, D.L.J.; Zhang, J.; Subedi, R.; Bou\u00e9tard, V.; Hiebert, S.; Ewanuk, R.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2001<\/strong>, 66<\/i>, 1233-1241 (DOI<\/a>).\"\"<\/li>\n \t
  138. Preparation of Polycyclic Systems by Sequential 5-Exo-Digonal <\/i>Radical Cyclization, 1,5-Hydrogen Transfer from Silicon, and 5-EndoTrigonal<\/i> Cyclization, Clive, D.L.J.; Yang, W.; MacDonald, A.; Wang, Z.; Cantin, M.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2001<\/strong>, 66<\/i>, 1966-1983 (DOI<\/a>).\"\"<\/li>\n \t
  139. A synthesis of puraquinonic acid, Hisaindee, S.; Clive, D.L.J. Tetrahedron Lett<\/em>. 2001<\/strong>, 42<\/i>, 2253-2255 (DOI<\/a>).\"\"<\/li>\n \t
  140. Tandem ring-closing metathesis-radical cyclization based on 4-(phenylseleno)butanal and methyl 3-(phenylseleno)propanoate \u2013a route to bicyclic compounds, Clive, D.L.J.; Cheng, H. Chem.\u00a0<\/i>Commun<\/em>. 2001<\/strong>, 605-606 (DOI<\/a>).\"\"<\/li>\n \t
  141. Stereocontrolled formation of spiro enones by radical cyclization of bromo acetals, Clive, D.L.J.; Huang, X. Tetrahedron\u00a0<\/em>2001<\/strong>, 57<\/i>, 3845-3858 (DOI<\/a>).\"\"<\/li>\n \t
  142. Synthesis and in vitro activity of a non-epimerizable analog of the angiotensin-converting enzyme inhibitor A58365A, Clive, D.L.J.; Yang, H.; Lewanczuk, R.Z. C.R. Acad. Sci., Paris,<\/i> Chimie\/Chemistry<\/em> 2001<\/strong>, 4<\/i>, 505-512 (DOI<\/a>).\"\"<\/li>\n \t
  143. Synthesis of (+)-Juruenolide C: Use of a Sequential 5-Exo-Diagonal <\/i>Radical Cyclization, 1,5-lntramolecular Hydrogen Transfer, and 5-Endo-Trigonal<\/i> Cyclization, Clive, D.L.J.; Ardelean, E.-S. J.\u00a0<\/i>Org. Chem<\/em>. 2001<\/strong>, 66<\/i>, 4841-4844 (DOI<\/a>).\"\"<\/li>\n \t
  144. Synthesis of Biaryls by lntramolecular Radical Transfer in Phosphinates, Clive, D.L.J., Kang, S. J.\u00a0<\/i>Org. Chem<\/em>. 2001<\/strong>, 66<\/i>, 6083-6091 (DOI<\/a>).\"\"<\/li>\n \t
  145. Synthesis of the racemic tetracyclic core of CP-225,917 – a model compound lacking the sidearms of the natural product, Clive, D.L.J.; Sun, S. Tetrahedron Lett<\/em>. 2001<\/strong>, 42<\/i>, 6267-6270 (DOI<\/a>).\"\"<\/li>\n \t
  146. Synthesis of the Naturally Occurring ACE Inhibitors A58365A and A58365B, and of an Unnatural but Biologically Active Analog, Clive, D.L.J.; Coltart, D.M.; Zhou, Y.; de Lima, D.P.; Yang, H.; Lewanczuk, R.Z. In Actualite de Chimie Therapeutique; French Society of Medicinal Chemistry<\/em> 2002<\/strong>, 28<\/i>, 21-50.\"\"<\/li>\n \t
  147. A Tin Hydride Designed to Facilitate Removal of Tin Species from Products of Stannane-Mediated Radical Reactions, Clive, D.L.J.; Wang, J. J. Org. Chem<\/i>. 2001<\/b>, 67<\/i>, 1192-1198 (DOI<\/a>).\"\"<\/li>\n \t
  148. Synthesis of the racemic tetracyclic core of CP-225,917: use of a strain-assisted Cope rearrangement, Clive, D.L.J.; Ou, L. Tetrahedron Lett<\/em>. 2002<\/strong>, 43<\/i>, 4559-4563 (DOI<\/a>).\"\"<\/li>\n \t
  149. Synthesis of the bicyclic dienone core of the antitumor agent ottelione B, Clive, D.L.J.; Fletcher S.P.\u00a0Chem. Commun<\/em>. 2002<\/strong>, 1940-1941 (DOI<\/a>).\"\"<\/li>\n \t
  150. A Free Radical Method for Reduction of Cyclohexanones – Preferential Formation of Equatorial Alcohols, Clive, D.L.J.; Cheng, H. Synth.\u00a0<\/i>Commun<\/em>. 2003<\/strong>, 33<\/i>, 1951-1961 (DOI<\/a>).\"\"<\/li>\n \t
  151. Synthesis of (+)-puraquinonic acid, Clive, D.L.J.; Yu, M.\u00a0Chem. Commun<\/em>. 2002<\/strong>, 2380-2381 (DOI<\/a>).\"\"<\/li>\n \t
  152. Studies related to furopyridinone antibiotics, Synthesis of 2-epi<\/em>-CJ-16,170, Clive, D.L.J.; Huang, X. Tetrahedron<\/em> 2002<\/strong>, 58<\/i>, 10243-10250 (DOI<\/a>).\"\"<\/li>\n \t
  153. Formal radical cyclization onto benzene rings – a general method proceeding via cross-conjugated dienones, Clive, D.L.J.; Fletcher, S.P. and (in part) Zhu, M.\u00a0Chem. Commun<\/em>. 2003<\/strong>, 526-527 (DOI<\/a>).\"\"<\/li>\n \t
  154. Synthetic studies related to CP-225,917, Clive, D.L.J.; Sgarbi, P.W.M.; He, X.; Sun, S.; Zhang, J.; Ou, L. Can. J.\u00a0<\/i>Chem<\/em>. 2003<\/strong>, 81<\/i>, 811-824 (DOI<\/a>).\"\"<\/li>\n \t
  155. Stereospecific Total Synthesis of the Antiviral Agent Hamigeran B – Use of Large Silyl Groups to Enforce Facial Selectivity and to Suppress Hydrogenolysis, Clive, D.L.J.; Wang, J. Angew. Chem. Int. Ed.<\/em> 2003<\/strong>, 42<\/i>, 3406-3409 (DOI<\/a>).\"\"<\/li>\n \t
  156. First synthesis of the antifungal and antibacterial agent cladobotryal, Clive, D.L.J.; Huang, X.\u00a0Chem. Commun<\/em>. 2003<\/strong>, 2062-2063 (DOI<\/a>).\"\"<\/li>\n \t
  157. Derivatized Amino Acids Relevant to Native Peptide Synthesis by Chemical Ligation and Acyl Transfer, Clive, D.L.J.; Hisaindee, S.; Coltart, D.M.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2003<\/strong>, 68<\/i>, 9247-9254 (DOI<\/a>).\"\"<\/li>\n \t
  158. Synthesis of (+)-nocardione A \u2013 use of formal radical cyclization onto a benzene ring, Clive, D.L.J.; Fletcher, S.P.\u00a0Chem. Commun<\/em>. 2003<\/strong>, 2464-2465 (DOI<\/a>).\"\"<\/li>\n \t
  159. Synthesis of natural (\u2013)-hamigeran B, Clive, D.L.J.; Wang, J. Tetrahedron Lett<\/em>. 2003<\/strong>, 44<\/i>, 7731-7733 (DOI<\/a>).\"\"<\/li>\n \t
  160. Model Studies and First Synthesis of the Antifungal and Antibacterial Agent Cladobotryal, Clive, D.L.J., Huang, X.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2004<\/strong>, 69<\/i>, 1872-1879 (DOI<\/a>).\"\"<\/li>\n \t
  161. Synthesis of (\u00b1)-Hamigeran B, (\u2013)-Hamigeran B, and (\u00b1)-1-epi<\/i>-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon\u2013Oxygen Bond from Hydrogenolysis, Clive, D.L.J., Wang, J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2004<\/strong>, 69<\/i>, 2773-2784 (DOI<\/a>).\"\"<\/li>\n \t
  162. Formal Radical Cyclization onto Benzene Rings: A General Method and Its Use in the Synthesis of ent<\/i>-Nocardione A, Clive, D.L.J., Fletcher, S.P., Liu, D. J.\u00a0<\/i>Org. Chem<\/em>. 2004<\/strong>, 69<\/i>, 3282-3293 (DOI<\/a>).\"\"<\/li>\n \t
  163. Synthesis of Optically Pure (+)-Puraquinonic Acid and Assignment of Absolute Configuration to Natural (\u2013)-Puraquinonic Acid. Use of Radical Cyclization for Asymmetric Generation of a Quaternary Center, Clive, D.L.J., Yu, M., Sannigrahi, M.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2004<\/strong>, 69<\/i>, 4116-4125 (DOI<\/a>).\"\"<\/li>\n \t
  164. Synthesis of the substituted spiro segment of halichlorine – use of radical cyclization and stereospecific cuprate addition to an \u03b1,\u03b2-unsaturated lactam, Yu, M.; Clive, D.L.J.; Yeh, V.S.C.; Kang, S.; Wang, J. Tetrahedron Lett<\/em>. 2004<\/strong>, 45<\/i>, 2879-2881 (DOI<\/a>).\"\"<\/li>\n \t
  165. [2.2.2]-Bicyclic systems relevant to synthetic studies on CP-225,917 \u2013 use of a new silylated cyclopentadiene, Clive, D.L.J., Cheng, H., Gangopadhyay, P., Huang, X., Prabhudas, B. Tetrahedron<\/em> 2004<\/strong>, 60<\/i>, 4205-4221 (DOI<\/a>).\"\"<\/li>\n \t
  166. A general method for making bicyclic compounds with nitrogen at a bridgehead – application to the halichlorine spiro subunit, Clive, D.L.J.; Yu, M.; Li, Z.\u00a0Chem. Commun<\/em>. 2005<\/strong>, 906-908 (DOI<\/a>).\"\"<\/li>\n \t
  167. Oxidation of p<\/em>-Aminophenols and Formal Radical Cyclization onto Benzene Rings: Formation of Benzo-Fused Nitrogen Heterocycles, Fletcher, S.P.; Clive, D.L.J.; Peng, J.; Wingert, D.A. Org. Lett<\/em>. 2005<\/strong>, 7<\/i>, 23-26 (DOI<\/a>).\"\"<\/li>\n \t
  168. Synthetic Chemistry of the Hamigerans. A Review, Clive, D.L.J.; Wang, J. Org. Prep. Proc<\/em>. Int<\/i>. 2005<\/strong>, 37<\/i>, 3-35 (DOI<\/a>).\"\"<\/li>\n \t
  169. Conversion of Furans into \u03b3-Hydroxybutenolides: Use of Sodium Chlorite, Clive, D.L.J.; Minarruzaman; Ou, L.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2004<\/strong>, 70<\/i>, 3318-3320 (DOI<\/a>).\"\"<\/li>\n \t
  170. Synthesis of a spirocyclic amine related to the marine natural products halichlorine and pinnaic acid, Clive, D.L.J.; Wang, J.; Yu, M. Tetrahedron Lett<\/em>. 2005<\/strong>, 46<\/i>, 2853-2855 (DOI<\/a>).\"\"<\/li>\n \t
  171. Synthetic Chemistry of Halichlorine and the Pinnaic Acids, Clive, D.L.J.; Yu, M.; Wang, J.; Yeh, V.S.C.; Kang, S. Chem. Rev<\/em>. 2005<\/strong>, 105<\/i>, 4483-4514 (DOI<\/a>).\"\"<\/li>\n \t
  172. A short synthetic route to the core structures of otteliones A and B, Clive, D.L.J.; Liu, D. Tetrahedron Lett<\/em>. 2005<\/strong>, 46<\/i>, 5305-5307 (DOI<\/a>).\"\"<\/li>\n \t
  173. Synthesis of the Core Structure of the Fungal Metabolite Benesudon: Use of Oxidative Decarboxylation, Clive, D.L.J.; Minaruzzaman; Yang, H. Org. Lett<\/em>. 2005<\/strong>, 7<\/i>, 5581-5583 (DOI<\/a>).\"\"<\/li>\n \t
  174. Carbocyclization by Radical Closure onto O<\/i>-Trityl Oximes: Dramatic Effect of Diphenyl Diselenide, Clive, D.L.J.; Pham, M.P.; Subedi, R.\u00a0J.\u00a0<\/em>Am. Chem. Soc.<\/em> 2007<\/strong>, 129<\/i>, 2713-2717 (DOI<\/a>).\"\"<\/li>\n \t
  175. Synthesis of the Otteliones A and B: Use of a Cyclopropyl Group as Both a Steric Shield and Vinyl Equivalent, Clive, D.L.J.; Liu, D. Angew. Chem. Int. Ed<\/em>. 2007<\/strong>, 46<\/i>, 3738-3740 (DOI<\/a>).\"\"<\/li>\n \t
  176. A convenient general method for the synthesis of hydroxy diacids, Chiruta, C.; Jachak, S.; Clive, D.L.J. Tetrahedron Lett<\/em>. 2007<\/strong>, 48<\/i>, 3141-3143 (DOI<\/a>).\"\"<\/li>\n \t
  177. Total synthesis of (\u2013)-conocarpan and assignment of the absolute configuration by chemical methods, Clive, D.L.J.; Stoffman, E.J.L. Chem. Commun<\/em>. 2007<\/strong>, 2151-2153 (DOI<\/a>).\"\"<\/li>\n \t
  178. HMBD: the Human Metabolome Database, Wishart, D.S.; Tzur, D.; Knox, C.; Eisner, R.; Guo, A.C.; Young, N.; Cheng, D.; Jewell, K.; Arndt, D.; Sawhney, S.; Fung, C.; Nikolai, L.; Lewis, M.; Coutouly, M. -A.; Forsythe, I.; Tang, P.; Shrivastava, S.; Jeroncic, K.; Stothard, P.; Amegbey, G.; Block, D.; Hau, D.D.; Wagner, J.; Miniaci, J.; Clements, M.; Gebremedhin, M.; Guo, N.; Zhang, Y.; Duggan, G.E.; Macinnis, G.D.; Weljie, A.M.; Dowlatabadi, R.; Bamforth, F.; Clive, D.; Greiner, R.; Li, L.; Marrie, T.; Sykes, B.D.; Vogel, H.J.; Querengesser, L. Nucleic Acids Res<\/em>. 2007<\/strong>, 35<\/i>, D521-D526 (DOI<\/a>).<\/li>\n \t
  179. lntramolecular Conjugate Displacement: A General Route to Hexahydroquinolizines, Hexahydroindolizines, and Related [m.n.0]-Bicyclic Structures with Nitrogen at a Bridgehead, Clive, D.L.J.; Li, Z.; Yu, M. Org. Chem<\/em>. 2007<\/strong>, 72<\/i>, 5608-5617 (DOI<\/a>).\"\"<\/li>\n \t
  180. Formation of Benzo-Fused Carbocycles by Formal Radical Cyclization onto an Aromatic Ring, Clive, D.L.J.; Sunasee, R. Org. Lett<\/em>. 2007<\/strong>, 9<\/i>, 2677-2680 (DOI<\/a>).\"\"<\/li>\n \t
  181. Synthesis of Dihydrooxepin Models Related to the Antitumor Antibiotic MPC1001, Peng, J.; Clive, D.L.J. Org. Lett<\/em>. 2007<\/strong>, 9<\/i>, 2939-2941 (DOI<\/a>).\"\"<\/li>\n \t
  182. All-Carbon lntramolecular Conjugate Displacement Reactions: an Effective Route to Carbocycles, Prabhudas, B.; Clive, D.L.J. Angew. Chem. Int. Ed<\/em>. 2007<\/strong>, 46<\/i>, 9295-9297 (DOI<\/a>).\"\"<\/li>\n \t
  183. Oxidative Decarboxylation as a Route to Ketene Acetals: Assignment of Relative and Absolute Stereochemistry to the Fungal Metabolite Benesudon by Total Synthesis, Clive, D.L.J.; Minaruzzaman Org. Lett<\/em>. 2007<\/strong>, 9<\/i>, 5315-5317 (DOI<\/a>).\"\"<\/li>\n \t
  184. Synthesis of Diverse 2,3-Dihydroindoles, 1,2,3,4-Tetrahydroquinolines and Benzo-Fused Azepines by Formal Radical Cyclization onto Aromatic Rings, Clive, D.L.J.; Peng, J.; Fletcher, S.P.; Ziffle, V.E.; Wingert, D.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2008<\/strong>, 73<\/i>, 2330-2344 (DOI<\/a>).\"\"<\/li>\n \t
  185. Synthesis of the Potent Anticancer Agents Ottelione A and Ottelione B in Both Racemic and Natural Optically Pure Forms, Clive, D.L.J.; Liu, D.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2008<\/strong>, 73<\/i>, 3078-3087 (DOI<\/a>).\"\"<\/li>\n \t
  186. Formal radical closure onto aromatic rings\u2014a general route to carbocycles, Clive, D.L.J.; Sunasee, R.; Chen, Z. Org. Biomol. Chem<\/em>. 2008<\/strong>, 6<\/i>, 2434-2441 (DOI<\/a>).\"\"<\/li>\n \t
  187. Synthesis of (\u2013)-conocarpan by two routes based on radical cyclization and establishment of its absolute configuration, Clive, D.L.J.; Stoffman, E.J.L. Org. Biomol. Chem<\/em>. 2008<\/strong>, 6<\/i>, 1831-1842 (DOI<\/a>).\"\"<\/li>\n \t
  188. [1-(Phenylseleno)alkyl]stannanes\u2014Mixed Selenium\/Tin Analogs of Acetals: Preparation from \u03b1-Hydroxystannanes and Use for Generating Selenium-Stabilized Carbanions, Fernandopulle, S.C.; Clive, D.L.J.; Yu, M. J. Org. Chem<\/em>. 2008<\/strong>, 73<\/i>, 6018-6021 (DOI<\/a>).\"\"<\/li>\n \t
  189. The Naturally Occurring Ketene Acetal Benesudon: Total Synthesis and Assignment of Relative and Absolute Stereochemistry, Clive, D.L.J.; Minaruzzaman; Yang, H.\u00a0J. Org. Chem<\/em>.\u00a02008<\/strong>, 73<\/i>, 6743-6752 (DOI<\/a>).\"\"<\/li>\n \t
  190. A Route to 1,4-Disubstituted Aromatics and its Application to the Synthesis of the Antibiotic Culpin, Sunasee, R.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2008<\/strong>, 73<\/i>, 8016-8020 (DOI<\/a>).\"\"<\/li>\n \t
  191. <\/a>Asymmetric Synthesis of the ABC-Ring System of the Antitumor Antibiotic MPC1001, Peng, J.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2009<\/strong>, 74<\/i>, 513-519 (DOI<\/a>).\"\"<\/li>\n \t
  192. Conversion of Weinreb Amides into Benzene Rings Incorporating the Amide Carbonyl Carbon, Clive, D.L.J.; Pham, M.P.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2009<\/strong>, 74<\/i>, 1685-1690 (DOI<\/a>).\"\"<\/li>\n \t
  193. Formation of Carbocycles by lntramolecular Conjugate Displacement: Scope and Mechanistic Insights, Wang, L.; Prabhudas, B.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Am. Chem. Soc<\/em>. 2009<\/strong>, 131<\/i>, 6003-6012 (DOI<\/a>).\"\"<\/li>\n \t
  194. The coumarin\u2192indole Transformation\u2014a method for preparing 4-halo-5-hydroxyindoles from coumarins, Stoffman, E.J.L.; Clive, D.L.J. Org. Biomol. Chem<\/em>. 2009<\/strong>, 7<\/i>, 4862-4870 (DOI<\/a>).\"\"<\/li>\n \t
  195. Total Synthesis of the Marine Alkaloid Halichlorine: Development and Use of a General Route to Chiral Piperidines, Liu, D.; Acharya, H.P.; Yu, M.; Wang, J.; Yeh, V.S.C.; Kang, S.; Chiruta, C.; Jachak, S.M.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2009<\/strong>, 74<\/i>, 7417-7428 (DOI<\/a>).\"\"<\/li>\n \t
  196. Desymmetrization of 4-hydroxy-2,5-cyclohexadienones by radical cyclization: synthesis of optically pure \u03b3-lactones, Sunasee, R.; Clive, D.L.J. Chem. Commun<\/em>. 2010<\/strong>, 46<\/i>, 701-703 (DOI<\/a>).\"\"<\/li>\n \t
  197. Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine, Stoffman, E.J.; Clive, D.L.J. Tetrahedron<\/em> 2010<\/strong>, 66<\/i>, 4452-4461 (DOI<\/a>).\"\"<\/li>\n \t
  198. 2,6-Disubstituted and 2,2,6-Trisubstituted Piperidines from Serine: Asymmetric Synthesis and Further Elaboration, Acharya, H.P.; Clive, D.L.J. J. Org. Chem<\/em>. 2010<\/strong>, 75<\/i>, 5223-5233 (DOI<\/a>).\"\"<\/li>\n \t
  199. Formation of Unusual Seven-Membered Heterocycles Incorporating Nitrogen and Sulfur by lntramolecular Conjugate Displacement, Chen, Z.; Clive, D.L.J. J. Org. Chem<\/em>. 2010<\/strong>, 75<\/i>, 7014-7017 (DOI<\/a>).\"\"<\/li>\n \t
  200. Conversion of 1,4-Diketones into para<\/i>-Disubstituted Benzenes, Ziffle, V.E.; Cheng, P.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2010<\/strong>, 75<\/i>, 8024-8038 (DOI<\/a>).\"\"<\/li>\n \t
  201. The [[(tert<\/i>-Butyl)dimethylsilyl]oxy]methyl Group for Sulfur Protection, Wang, L.; Clive, D.L.J. Org. Lett<\/em>. 2011<\/strong>, 13<\/i>, 1734-1737 (DOI<\/a>).\"\"<\/li>\n \t
  202. The Marine Alkaloid Halichlorine: Its Defenses and its Defeat, Clive, D.L.J. In Strategies and Tactics in Organic Synthesis<\/em>; Harmata, M., Ed.; Vol. 8, Academic Press: Burlington, 2012<\/strong>, pp. 25-54 (DOI<\/a>).\"\"<\/li>\n \t
  203. Synthetic studies related to MPC1001: formation of a model epidithiodiketopiperazine, Wang, L.; Clive, D.L.J. Tetrahedron Lett<\/em>. 2012<\/strong>, 53<\/i>, 1504-1506 (DOI<\/a>).\"\"<\/li>\n \t
  204. Reagent for Divalent Sulfur Protection: Preparation of 4-Methylbenzenesulfonothioic Acid, S-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl] Ester, Wang, L.; Clive, D.L.J. Org. Synth<\/em>. 2013<\/strong>, 90<\/i>, 10-24 (DOI<\/a>).\"\"<\/li>\n \t
  205. Formation of Optically Pure Cyclic Amines by lntramolecular Conjugate Displacement, Cheng, P.; Clive, D.L.J. J. Org. Chem<\/em>. 2012<\/strong>, 77<\/i>, 3348-3364 (DOI<\/a>).\"\"<\/li>\n \t
  206. A Dieckmann Cyclization Route to Piperazine-2,5-diones, Aboussafy, C.L.; Clive, D.L.J. J. Org. Chem<\/em>. 2012<\/strong>, 77<\/i>, 5125-5131 (DOI<\/a>).\"\"<\/li>\n \t
  207. Racemic marinopyrrole B by total synthesis, Cheng, P.; Clive, D.L.J.; Fernandopulle, S.; Chen, Z. Chem. Commun<\/em>. 2013<\/strong>, 49<\/i>, 558-560 (DOI<\/a>).\"\"<\/li>\n \t
  208. Synthetic Studies on CP-225,917 and CP-263,114: Access to Advanced Tetracyclic Systems by lntramolecular Conjugate Displacement and [2,3]-Wittig Rearrangement, Malihi, F.; Clive, D.L.J.; Chang, C.-C.; Minaruzzaman Org. Chem<\/em>. 2013<\/strong>, 78<\/i>, 996-1013 (DOI<\/a>).\"\"<\/li>\n \t
  209. Asymmetric synthesis of carbocycles: use of intramolecular conjugate displacement, Sreedharan, D.T.; Clive, D.L.J. Org. Biomol. Chem<\/em>. 2013<\/strong>, 11<\/i>, 3128-3144 (DOI<\/a>).\"\"<\/li>\n \t
  210. The marinopyrroles, Clive, D.L.J.; Cheng, P. Tetrahedron<\/em> 2013<\/strong>, 69<\/i>, 5067-5078 (DOI<\/a>).\"\"<\/li>\n \t
  211. A General Route of 1,3′-Bipyrroles, Cheng, P.; Shao, W.; Clive, D.L.J.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2013<\/strong>, 78<\/i>, 11866-11873 (DOI<\/a>).\"\"<\/li>\n \t
  212. Synthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones, Shao, W.; Clive, D.L.J. J. Org. Chem<\/em>. 2015<\/strong>, 80<\/i>, 3211-3216 (DOI<\/a>).\"\"<\/li>\n \t
  213. Synthesis of (+)-lpalbidine Based on 6-exo-trig<\/i> Radical Cyclization of a \u03b2-Amino Radical, Chea, J.; Clive, D.L.J. J. Org. Chem<\/em>. 2015<\/strong>, 80<\/i>, 10294-10298 (DOI<\/a>).\"\"<\/li>\n \t
  214. A Family of Routes to Substituted Phenols, Including Meta-Substituted Phenols, Shao, W.; Clive, D.L.J. J. Org. Chem<\/em>. 2015<\/strong>, 80<\/i>, 12280-12287 (DOI<\/a>).\"\"<\/li>\n \t
  215. [(tert<\/i>-Butyldi methylsilyl)oxy]methanethiol and [(tert<\/i>-Butyldiphenylsilyl)oxy]methanethiol\u2014nucleophilic protected H2<\/sub>S equivalents, Dong, S.; Clive, D.L.J.; Gao, J.-M. Tetrahedron Lett<\/em>. 2015<\/strong>, 56<\/i>, 6857-6859 (DOI<\/a>).\"\"<\/li>\n \t
  216. Conversion of cycloalk-2-enones into 2-methylcycloalkane-1,3-diones\u2014assessment of various Tamao-Fleming procedures and mechanistic insight into the use of the Me3<\/sub>SiMe2<\/sub>Si unit, Yu, G.; Clive, D.L.J. Org. Biomol. Chem<\/em>. 2016<\/strong>, 14<\/i>, 1653-1664 (DOI<\/a>).\"\"<\/li>\n \t
  217. Computations Reveal That Electron-Withdrawing Leaving Groups Facilitate lntramolecular Conjugate Displacement Reactions by Negative Hyperconjugation, Noey, E.L.; Jim\u00e9nez-Os\u00e9s, G.; Clive, D.L.J.; Houk, K.N.\u00a0J.\u00a0<\/em>Org. Chem<\/em>. 2016<\/strong>, 81<\/i>, 4290-4294 (DOI<\/a>).\"\"<\/li>\n \t
  218. Synthesis of models of the BC ring systems of MPC1001 and MPC1001F, Dong, S.; lndukuri, K.; Clive, D. L. J.; Gao, J.-M. Chem. Commun<\/em>. 2016<\/strong>, 52<\/i>, 8271-8274 (DOI<\/a>).\"\"<\/li>\n \t
  219. Formation of meta<\/i>-Substituted Phenols by Transition Metal-Free Aromatization: Use of 2-Bromocyclohex-2-en-1-ones, Yu, G.; Clive, D.L.J.\u00a0J. Org. Chem<\/em>. 2016<\/strong>, 81<\/i>, 8470-8484 (DOI<\/a>).\"\"<\/li>\n \t
  220. Formation of meta<\/i>-arylsulfanyl- and meta-(alkylsulfanyl)phenols from cyclohexane-1,3-diones, Do, N.V.T.; Patra, S.; Clive, D.L.J. Tetrahedron<\/em> 2018<\/strong>, 74<\/i>, 4343-4350 (DOI<\/a>).\"\"<\/li>\n \t
  221. Synthesis of phenolic components of Grains of Paradise, Hattori, H.; Mitsunaga, T.; Clive, D.L.J. Tetrahedron Lett<\/em>. 2019<\/strong>, 60<\/i>, 1989-1991 (DOI<\/a>).\"\"<\/li>\n \t
  222. Formation of Enol Ethers by Radical Decarboxylation of \u03b1-Alkoxy \u03b2-Phenylthio Acids, Palanivel, A.; Mubeen, S.; Warner, T.; Ahmed, N.; Clive, D.L.J. J. Org. Chem<\/em>. 2019<\/strong>, 84<\/i>, 12542-12552 (DOI<\/a>).\"\"<\/li>\n \t
  223. Formation of 3-Aminophenols from Cyclohexane-1,3-diones, Szymor-Pietrzak, D.; Khan, M.N.; Pag\u00e8s, A.; Kumar, A.; Depner, N.; Clive, D.L.J. J. Org. Chem<\/em>. 2021<\/strong>, 86<\/i>, 619-631 (DOI<\/a>).\"\"<\/li>\n \t
  224. A mild alternative to the classical Ullmann coupling for preparation of 3-aryloxy phenols, Duvvuru, B.; Amankulova, D.; Gauden, S.; Haffemayer, T.; Clive, D.L.J. Tetrahedron<\/em> 2023<\/strong>, 133<\/i>, 133264 (1-13) (DOI<\/a>).\"\"<\/li>\n<\/ol>\n<\/a>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
    \n\t\t\t\t\t
    \n\t\t
    \n\t\t\t\t
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    Patents\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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    1. Synthesis of Cholesterol-Lowering Agents. Clive, D.L.J.; Wee, A.G.H.; Keshava Murthy, K.S. U.S. Patent 5,072,002 (10 December 1991).<\/li>\n \t
    2. Deoxygenation of Cis Vicinal Diols to make Didehydrodideoxy Nucleosides and Synthetic Intermediates. Clive, D.L.J.; Wickens, P.L. US Patent 5,410,033 (25 April, 1995).<\/li>\n \t
    3. Commercial Process for the Manufacture of Fluconozole and Intermediates Useful in the Manufacture Thereof. Keshava Murthy, K.S.; Clive, D.L.J.; Weeratunga, G.; Norris, D.; Horne, S. Canadian Patent 2,139,079 (28 May, 1996).<\/li>\n \t
    4. Synthesis of (\u00b1)-calicheamicinone, precursors, intermediates and derivatives. Clive, D.L.J.; Daigneault, S.; Bo, Y.; Tao, Y. PCT WO 97\/41109 (6 November, 1997).<\/li>\n<\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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      Encyclopedia Articles<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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      <\/a><\/p>

      1. 4-Chlorophenyl Chlorothionoformate. Postema, M.H.D.; Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 2, 1201.<\/li>
      2. (Phenylseleno)acetaldehyde. Magnuson, S.R.; Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 6, 4015-4016.<\/li>
      3. Sodium O,O<\/i>-Diethyl Phosphorotelluroate. Wickens, P.L.; Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 7, 4549-4551.<\/li>
      4. Triphenylphosphine Selenide. Mayhew, D.L.; Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 8, 5398-5399.<\/li>
      5. Triphenylphosphine Sulfide. Mayhew, D.L.; Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 8, 5399.<\/li>
      6. Triphenyl Thioborate. Wickens, P.L.; Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 8, 5419.<\/li>
      7. Triphenylstannane, Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 8, 5412-5416.<\/li>
      9. Diphenyl[2-(4-pyridyl)ethyl]tin hydride.\u00a0 Yang, W.; Clive, D.L.J. “Electronic Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley:\u00a0 New York, 2003.<\/span><\/div><\/li><\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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        \n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"

        Publications 1968-1979 Publications 1980-1989 Publications 1990-1999 Publications 2000-2009 Publications 2009- Patents Encyclopedia Articles Publications Chemistry of Tetracyclines, Clive, D.L.J. Quart […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"site-sidebar-layout":"no-sidebar","site-content-layout":"","ast-site-content-layout":"full-width-container","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"disabled","ast-breadcrumbs-content":"","ast-featured-img":"disabled","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"class_list":["post-1090","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/pages\/1090","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/comments?post=1090"}],"version-history":[{"count":717,"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/pages\/1090\/revisions"}],"predecessor-version":[{"id":2704,"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/pages\/1090\/revisions\/2704"}],"wp:attachment":[{"href":"https:\/\/www.chem.ualberta.ca\/~clive\/wp-json\/wp\/v2\/media?parent=1090"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}