Publications 1968-1979

Publications 1980-1989

Publications 1990-1999

Publications 2000-2009

Publications 2009-

Patents

Encyclopedia Articles

Publications

  1. Chemistry of Tetracyclines, Clive, D.L.J. Quart Rev. (London) 1968, 22, 435-456 (DOI).
  2. A New Method for Conversion of Aldoximes into Nitriles: Use of Chlorothionoformates, Clive, D.L.J. J. Chem. Soc., Chem. Comm. 1970, 1014-1015 (DOI).
  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. 1971, 1112-1113 (DOI).
  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. Soc. (C) 1971, 2193-2203 (DOI).
  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. Soc. (C) 1971, 2204-2215 (DOI).
  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. 1972, 773-774 (DOI).
  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. 1973, 253 (DOI).
  8. Fragmentation of Selenoxides: a New Method for Dehydrogenation of Ketones, Clive, D.L.J. J. Chem. Soc., Chem. Comm. 1973, 695-696 (DOI).
  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. 1974, 100 (DOI).
  10. Polyamide Supports for Polypeptide Synthesis, Atherton, E.; Clive, D.L.J.; Sheppard, R.C. J. Am. Chem. Soc. 1975, 97, 6584-6585 (DOI).
  11. Synthesis of Some Polypeptides on Polyamide Supports, Atherton, E.; Clive, D.L.J.; East, D.A.; Sheppard, R.C. Peptides 1976, Proceedings of the Fourteenth European Peptide Symposium, Wépion, Belgium, April 11-171976, pp. 291-297.
  12. New Route to Bicyclic Lactones: Use of Benzeneselenenyl Chloride, Clive, D.L.J.; Chittattu, G. J. Chem. Soc., Chem. Comm. 1977, 484-485 (DOI).
  13. A new route to ring-fused tetrahydrofurans: reactions of ∆4-unsaturated alcohols with phenylselenenyl chloride, Clive, D.L.J.; Chittattu, G.; Wong, C.K. Can. J. Chem. 1977, 55, 3894-3897 (DOI).
  14. New Method for Deoxygenation of Sulphoxides: Use of O,O-Diethyl Hydrogenphosphoroselenoate, Clive, D.L.J.; Kiel, W.A.; Menchen, S.M.; Wong, C.K. J. Chem. Soc., Chem. Comm. 1977, 657-658 (DOI).
  15. New and Selective Method for Deoxygenating Epoxides: Use of the Organic Tellurium Reagent Sodium O,O-Diethyl Phosphorotelluroate, Clive, D.L.J.; Menchen, S.M. J. Chem. Soc., Chem. Comm. 1977, 658-659 (DOI).
  16. Cyclofunctionalisation of ortho-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. 1977, 725-727 (DOI).
  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. J. Chem. Soc., Chem. Comm. 1978, 41-42 (DOI).
  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. Chem. Soc., Chem. Comm. 1978, 379-380 (DOI).
  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. 1978, 356 (DOI).
  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. 1978, 441-442 (DOI).
  21. Modern Organoselenium Chemistry, Clive, D.L.J. Tetrahedron 1978, 34, 1049-1132 (DOI).
  22. Selenium Reagents for Organic Synthesis, Clive, D.L.J. Aldrichimica Acta 1978, 11, 43-49.
  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. 1978, 770-771 (DOI).
  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. 1979, 168-169 (DOI).
  25. New Route to Selenoacetals: Exchange Reaction between Acetals and Tris(phenylseleno)borane, Clive, D.L.J.; Menchen, S.M. J. Org. Chem. 1979, 44, 1883-1885 (DOI).
  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. 1979, 44, 4279-4285 (DOI).
  27. 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, pp. 43-68.
  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 1980, 36, 1399-1408 (DOI).
  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. 1980, 102, 4438-4447 (DOI).
  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. 1980, 45, 2120-2126 (DOI).
  31. Alkali Metal O,O-Diethyl Phosphorotelluroates, a Reagent Class for Deoxygenation of Epoxides, Especially Terminal Epoxides, Clive, D.L.J.; Menchen, S.M. J. Org. Chem. 1980, 45, 2347-2354 (DOI).
  32. Generation of Carbon-Carbon Double Bonds from β-Oxygenated Phenylseleno, Phenylthio, and lodo Species. A New Use for the Chlorotrimethylsilane-Sodium Iodide Reagent, Clive, D.L.J.; Kalè, V.N. J. Org. Chem. 1981, 46, 231-234 (DOI).
  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, pp. 112-126.
  34. New Method for Preparing β,γ-Unsaturated Ketones: Use of Phenylselenoacetaldehyde, Clive, D.L.J.; Russell, C.G. J. Chem. Soc., Chem. Comm. 1981, 434-436 (DOI).
  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. 1 1981, 529-537 (DOI).
  36. Conjugate Addition of Methyl Groups to α,β-Unsaturated Aldehydes: Use of Me5Cu3Li2, Clive, D.L.J.; Farina, V.; Beaulieu, P.L. J. Chem. Soc., Chem. Comm. 1981, 643-644 (DOI).
  37. Dehalogenation of α-Chloro and α-Bromo Ketones. Use of Sodium O,O-Diethyl Phosphorotelluroate, Clive, D.L.J.; Beaulieu, P.L. J. Org. Chem. 1982, 47, 1124-1126 (DOI).
  38. α Vinylation of Ketones. A General Method Using (Phenylseleno)acetaldehyde, Clive, D.L.J.; Russell, C.G.; Suri, S.C. J. Org. Chem. 1982, 47, 1632-1641 (DOI).
  39. New Method for Coupling Allylic Halides: Use of Te2– Species, Clive, D.L.J.; Anderson, P.C.; Moss, N.; Singh, A. J. Org. Chem. 1982, 47, 1641-1647 (DOI).
  40. Me5Cu3Li2: A Reagent for Conjugate Methylation of α,β-Unsaturated Aldehydes, Clive, D.L.J.; Farina, V.; Beaulieu, P.L. J. Org. Chem. 1982, 47, 2752-2582 (DOI).
  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. 1982, 828-830 (DOI).
  42. Formation of Carbon-Carbon Bonds by Ring Closure of β-Phenylselenocrotonates, Clive, D.L.J.; Beaulieu, P.L. J. Chem. Soc., Chem. Commun. 1983, 307-309 (DOI).
  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. Soc.1983, 105, 6429-6436 (DOI).
  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. 1983, 24, 1373-1376 (DOI).
  45. Synthesis of Ketones by Cyclization of Cyano and Acetylenic Radicals: Use of δ-Hydroxy Nitriles and δ- or ε-Hydroxy Acetylenes, Clive, D.L.J.; Beaulieu, P.L.; Set, L. J. Org. Chem.1984, 49, 1313-1314 (DOI).
  46. Studies Related to Thromboxane A2: A Formal Synthesis of Optically Active 9α,11α-Thiathromboxane A2 Methyl Ester from Levoglucosan, Kalè, V.N.; Clive, D.L.J. J. Org. Chem. 1984, 49, 1554-1563 (DOI).
  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. 1984, 534-536 (DOI).
  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. 1984, 25, 2101-2104 (DOI).
  49. 2-(Phenylseleno)prop-2-enenitrile: a Three-carbon Unit for Radical Cyclization, Angoh, A.G.; Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1985, 941-942 (DOI).
  50. Radical Annulation: A Method for Preparation of Carbocycles, Angoh, A.G.; Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1985, 980-982 (DOI).
  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., J. Chem. Commun. 1985, 1205-1207 (DOI).
  52. Synthetic Studies Related to Compactin: Use of Tri-O-acetyl-d-glucal for Preparation of Chiral Cyclohexenes, Prasad, J.S.; Clive, D.L.J.; da Silva, G.V.J. J. Org. Chem. 1986, 51, 2717-2721 (DOI).
  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. J. Chem. Soc., Chem. Commun. 1986, 588-589 (DOI).
  54. Synthesis of Spiro-compounds Related to Fredericamycin A, Bennett, S.M.; Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1986, 878-880 (DOI).
  55. Synthesis of Heterocyclic Compounds Related to Fredericamycin A – the Cyclopent[g]isoquinoline System, Clive, D.L.J.; Sedgeworth, J. J. Heterocyclic Chem. 1987, 24, 509-511 (DOI).
  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. J. Org. Chem. 1987, 52, 1339-1342 (DOI).
  57. Rules for Ring Fusion Geometry and the Preparation of trans– or cis-Fused Bicyclic Compounds by Radical Closure, Clive, D.L.J.; Cheshire, D.R.; Set, L. J. Chem. Soc., Chem. Commun. 1987, 353-355 (DOI).
  58. Construction of Five-Membered Rings by Michael Addition–Radical Cyclization, Clive, D.L.J.; Boivin, T.L.B.; Angoh, A.G. J. Org. Chem. 1987, 52, 4943-4953 (DOI).
  59. On Baldwin’s Kinetic Barrier Against 5-(Enol-endo)-exo-trigonal Closures: a Comparison of Ionic and Analogous Radical Reactions, and a New Synthesis of Cyclopentanones, Clive, D.L.J.; Cheshire, D.R. J. Chem. Soc., Chem. Commun. 1987, 1520-1523 (DOI).
  60. Total Synthesis of Both (+)-Compactin and (+)-Mevinolin. A General Strategy Based on the Use of a Special TiCl3/C8K 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. J. Am. Chem. Soc. 1988, 110, 6914-6916 (DOI).
  61. Synthetic methodology involving radical cyclization: spiro compounds and α-oxo radicals, Clive, D.L.J. Pure Appl. Chem. 1988, 60, 1645-1654 (DOI).
  62. Formation of Cis-Fused Cyclopentanoids by Michael Addition and Radical Cyclization, Clive, D.L.J.; Boivin, T.L.B. J. Org. Chem. 1989, 54, 1997-2003 (DOI).
  63. Synthetic Applications of Radical Ring-Opening: Use of Cyclopropylmethyl Radicals, Clive, D.L.J.; Daigneault, S. J. Chem. Soc., Chem. Commun. 1989, 332-335 (DOI).
  64. Conversion of Olefins into Five-membered Nitrogen Heterocycles by Radical Cyclization, Clive, D.L.J.; Mohammed, A.Y. Heterocycles 1989, 28, 1157-1167 (DOI).
  65. 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. 1990, 112, 3018-3028 (DOI).
  66. Synthesis of (±)-Frullanolide: An Application of Radical Closure, Clive, D.L.J.; Joussef, A.C. J. Org. Chem. 1990, 55, 1096-1098 (DOI).
  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. J. Org. Chem. 1990, 55, 1786-1792 (DOI).
  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. J. Chem. Soc., Perkin Trans. 1 1990, 2099-2108 (DOI).
  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. Chem. Soc., Chem. Commun. 1990, 509-511 (DOI).
  70. Construction of trans-Ring-fused Compounds by Radical Cyclization, Clive, D.L.J.; Manning, H.W.; Boivin, T.L.B. J. Chem. Soc., Chem. Commun. 1990, 972-974 (DOI).
  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. 1991, 31, 211-213 (DOI).
  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. 1 1991, 1433-1444 (DOI). [See J. Chem. Soc., Perkin Trans. 1 1992, 739 for correction of typographical error.]
  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.  J. Org. Chem. 1991, 56, 3801-3814 (DOI).
  74. Short Synthesis of (±)-5-(3-Furyl)octahydro-8-methylindolizines, Alkaloids Related to a Component of Castoreum. Use of Radical Cyclization, Clive, D.L.J.; Bergstra, R.J. J. Org. Chem. 1991, 56, 4976-4977 (DOI).
  75. Sequential Radical Ring Closure-Radical Ring Opening: Use in the Preparation of Benzofurans, Clive, D.L.J.; Daigneault, S. J. Org. Chem. 1991, 56, 5285-5289 (DOI).
  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. J. Chem. Soc., Perkin Trans. 1 1991, 2797-2799 (DOI).
  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. 1991, 56, 6447-6458 (DOI). (See J. Org. Chem. 1993, 58, 3472 for correction of typographical error.)
  78. Radical Cyclizations of Geminal Radical Precursors, Clive, D.L.J.; Cole, D.C. J. Chem. Soc., Perkin Trans. 1 1991, 3263-3270 (DOI).
  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. 1991, 32, 7159-7160 (DOI).
  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. J. Chem. Soc., Chem. Commun. 1991, 1755-1757 (DOI).
  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; Vol. 11, 335-377.
  82. Total Synthesis of Crystalline (±)-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. Chem. Soc., Chem. Commun. 1992, 1489-1490 (DOI).
  83. Synthesis of Carbazomycin B, Clive, D.L.J.; Etkin, N.; Joseph, T.; Lown, J.W. J. Org. Chem. 1993, 58, 2442-2445 (DOI).
  84. trans Ring-fused Bicyclic Structures by 6-exo-Trigonal Radical Closure: Use of the Triethylborane-Stannane-Air System for lntramolecular Radical Addition to Aldehydes, Clive, D.L.J.; Postema, M.H.D. J. Chem. Soc., Chem. Commun. 1993, 429-430 (DOI). [See J. Chem. Soc., Chem. Commun. 1993, 1240 for correction of typographical error.)
  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 1993, 49, 7917-7930 (DOI).
  86. Formal Preparation of Semisynthetic Analogues of the Cholesterol-lowering Agent Mevinolin, Clive, D.L.J.; Zhang, C. J. Chem. Soc., Chem. Commun. 1993, 647-649 (DOI).
  87. A General Method for Iterative Cyclopentannulation: Sequential Use of Claisen Rearrangement and Radical Enyne Closure, Clive, D.L.J.; Manning, H.W. J. Chem. Soc., Chem. Commun. 1993, 666-667 (DOI).
  88. Reaction of cis-Vicinal Dimesylates with Te2–: a Method for converting cis-Vicinal Diols into Olefins and its Use in the Preparation of 2′,3′-Didehydro-2′,3′-dideoxynucleosides, Clive, D.L.J.; Wickens, P.L. J. Chem. Soc., Chem. Commun. 1993, 923-924 (DOI).
  89. Formation of trans Ring-Fused Compounds by an Alkylation-Radical Cyclization Sequence, Clive, D.L.J.; Manning, H.W.; Boivin, T.L.B.; Postema, M.H.D. J. Org. Chem. 1993, 58, 6857-6873 (DOI).
  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. 1994, 235-236 (DOI).
  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. J. Org. Chem. 1994, 59, 1396-1406 (DOI).
  92. Synthesis of α-Amino Acids by Addition of Putative Azido Radicals to α-Methoxy Acrylonitriles Derived From Aldehydes and Ketones, Clive, D.L.J.; Etkin. N. Tetrahedron Lett. 1994, 35, 2459-2462 (DOI).
  93. Total Synthesis of Crystalline (±)-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. 1994, 116, 11275-11286 (DOI).
  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. Organomet. Chem. 1995, 489, C35-C37 (DOI).
  95. Synthesis of the Sesquiterpene (±)-Ceratopicanol: Use of Radicals Derived from Epoxides, Clive, D.L.J.; Magnuson, S.R. Tetrahedron Lett. 1995, 36, 15-18 (DOI).
  96. Studies on the Degradation of Mevinolin and Compactin: A Formal Route to Semisynthetic Analogues, Clive, D.L.J.; Zhang, C. J. Org. Chem. 1995, 60, 1413-1427 (DOI).
  97. 5-endo-Trigonal Radical Cyclization – A General Procedure for Making Five-membered Rings, Clive, D.L.J.; Cantin, M. J. Chem. Soc., Chem. Commun. 1995, 319-320 (DOI).
  98. A Nitrogen-Containing Stannane for Free Radical Chemistry, Clive, D.L.J.; Yang, W. J. Org. Chem. 1995, 60, 2607-2609 (DOI).
  99. Total Synthesis of Crystalline (±)-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; Vol. 16, 27-74 (DOI).
  100. Preparation of a Semisynthetic Analogue of Mevinolin and Compactin, Clive, D.L.J.; Wickens, P.L.; da Silva, G.V.J. J. Org. Chem. 1995, 60, 5532-5536 (DOI).
  101. Wittig chain extension of unprotected carbohydrates: formation of carbohydrate-derived α,β-unsaturated esters, Railton, C.J.; Clive, D.L.J. Carbohydr. Res. 1996, 281, 69-77 (DOI).
  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 (±)-Ceratopicanol, Clive, D.L.J.; Magnuson, S.M.; Manning, H.M.; Mayhew, D.L. J. Org. Chem. 1996, 61, 2095-2108 (DOI).
  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 1996, 52, 6085-6116 (DOI).
  104. Synthesis of (±)-Calicheamicinone by Two Related Methods, Clive, D.L.J.; Bo, Y.; Tao. Y.; Daigneault, S.; Wu, Y.-J.; Meignan, G. J. Am. Chem. Soc. 1996, 118, 4904-4905 (DOI).
  105. Synthesis of crystalline (±)-A58365B – an inhibitor of angiotensin-converting enzyme, Clive, D.L.J.; Zhou, Y.; de Lima, D.P. Chem. Commun. 1996, 1463-1464 (DOI).
  106. Preparation of tetrahydrofuran, γ-lactone, chromanol, and pyrrolidine systems by sequential 5-exo-digonal radical cyclization, 1,5- hydrogen transfer from silicon, and 5-endo-trigonal cyclization, Clive, D.L.J.; Yang, W. Chem Commun. 1996, 1605-1606 (DOI).
  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 Vicinal Diols to Olefins, Clive, D.L.J.; Wickens, P.L.; Sgarbi, P.W.M. J. Org. Chem. 1996, 61, 7426-7437 (DOI).
  108. Formal synthesis of (–)-calicheamicinone and of (+)-calicheamicinone, Clive, D.L.J.; Selvakumar, N. Chem. Commun. 1996, 2543-2544 (DOI).
  109. Synthesis of the aromatic unit of calicheamicin Hu, Y.-Z.; Clive, D.L.J. J. Chem. Soc., Perkin Trans. 1 1996, 1421-1424 (DOI).
  110. Prepaparation of α-(2,2-diphenylhydrazino)- and α-(benzyloxyamino)lactones by radical cyclization: use of glyoxylic acid diphenylhydrazone and glyoxylic acid O-benzyloxime, Clive, D.L.J.; Zhang, Chem. Commun. 1997, 549-550 (DOI).
  111. Synthesis of 2′,3′-Didehydro-2′,3′-dideoxynucleosides by Reaction of 5′-O-Protected Nucleoside 2′,3′-Dimesylates with Lithium Arylselenolates, Clive, D.L.J.; Sgarbi, P.W.M., Wickens, P.L. J. Org. Chem. 1997, 62, 3751-3753 (DOI).
  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. J. Org. Chem.1997, 62, 7028-7032 (DOI).
  113. Synthesis of the carbobicyclic substructure of CP-225,917 and CP-263,114, Sgarbi, P.W.M.; Clive, D.L.J. Chem Commun. 1997, 2157-2158 (DOI).
  114. Synthesis of the Angiotensin-Converting Enzyme Inhibitor (±)-A58365A, Clive, D.L.J.; Coltart, D.M. Tetrahedron Lett. 1998, 39, 2519-2522 (DOI).
  115. A synthetic route from D-glucose to D-myo-inositol-1,4,5-tris(dihydrogenphosphate): use of an unusual ene reaction and the Bu2SnCl2/Bu2SnH2 reagent, Clive, D.L.J.; Xiao H.; Postema, M.H.D.; Mashimbye, M.J. Tetrahedron Lett. 1998, 39, 4231-4234 (DOI).
  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 Lett. 1998, 39, 4789-4792 (DOI).
  117. Synthesis of (±)-Calicheamicinone by Two Methods, Clive, D.L.J.; Bo, Y.; Tao, Y.; Daigneault, S.; Wu, Y.-J.; Meignan, G. J. Am. Chem. Soc. 1998, 120, 10332-10349 (DOI).
  118. Synthesis of C-Glycosyl Lactones and Protected C-Glycosyl Amino Acids: Use of Radical Cyclization, Zhang, J.; Clive, D.L.J. J. Org. Chem.1999, 64, 770-779 (DOI).
  119. Synthesis and X-Ray Crystal Structure of (–)-Calicheamicinone, Clive, D.L.J.; Bo, Y.; Selvakumar, N.; McDonald, R.; Santarsiero, B.D. Tetrahedron 1999, 55, 3277-3290 (DOI).
  120. Synthesis of the Angiotensin-Converting Enzyme Inhibitors (–)-A58365A and (–)-A58365B from a Common Intermediate, Clive, D.L.J.; Coltart, D.M.; Zhou, Y. J. Org. Chem. 1999, 64, 1447-1454 (DOI).
  121. Synthesis of (+)-Furanomycin: Use of Radical Cyclization, Clive, D.L.J.; Zhang, J. J. Org. Chem. 1999, 64, 1754-1757 (DOI).
  122. Applications of 5-Endo-trigonal Cyclization: Construction of Compounds Relevant to the Synthesis of Prostaglandins and Methyl epi-Jasmonate, Sannigrahi, M.; Mayhew, D.L.; Clive, D.L.J. J. Org. Chem. 1999, 64, 2776-2788 (DOI).
  123. Formal Synthesis of D-myo-lnositol-1,4,5-Tris(dihydrogen phosphate): Cyclization by an Unusual Ene Reaction and Use of the Bu2SnCl2/Bu 2SnH2 Reagent for Generating an Equatorial Alcohol, Clive, D.L.J.; He, X.; Postema, M.H.D.; Mashimbye, M.J. J. Org. Chem. 1999, 64, 4397-4410 (DOI).
  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. J. Heterocyclic Chem. 1999, 36, 653-658 (DOI).
  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. 1999, 40, 4605-4609 (DOI).
  126. Model Studies Related to CP-225,917: Stereocontrolled Generation of the Quaternary Center, Clive, D.L.J.; Zhang, J. Tetrahedron Lett. 1999, 41, 12059-12068 (DOI).
  127. Synthesis of racemic brevioxime, Clive, D.L.J.; Hisaindee, S. Chem. Commun. 1999, 2251-2252 (DOI).
  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. 1999, 40, 8503-8507 (DOI).
  129. Radical cyclization of O-trityl oximino esters—a ring closure that preserves the oxime function, Clive, D.L.J.; Subedi, R. Chem. Commun. 2000, 237-238 (DOI).
  130. Synthesis of biaryls by intramolecular radical transfer: use of phospinates, Clive, D.L.J.; Kang, S. Tetrahedron Lett. 2000, 41, 1315-1319 (DOI).
  131. Effect of Aryl Substituents on Rate of Desulfonylation of Aryl Alkyl Sulfones: Superiority of p-Fluorophenyl- and 2-Naphthyl Sulfones, Clive, D.L.J.; Yeh, V.S.C. Synth. Commun. 2000, 30, 3267-3274 (DOI).
  132. Synthesis of Racemic Brevioxime and Related Model Compounds, Clive, D.L.J.; Hisaindee, S. J. Org. Chem. 2000, 65, 4923-4929 (DOI).
  133. Synthetic studies on calicheamicin γ1I — Synthesis of (–)-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. 2000, 1341-1350 (DOI).
  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. 2000, 41, 6259-6263 (DOI).
  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. 2000, 3113-3121 (DOI).
  136. Synthesis of (±)-Puraquinonic Acid – an Inducer of Cell Differentiation, Clive, D.L.J.; Sannigrahi, M.; Hisaindee, S. J. Org. Chem. 2001, 66, 954-961 (DOI).
  137. Preparation of α-(2,2-Diphenylhydrazino)lactones and Related Compounds by Radical Cyclization: Use of Glyoxylic Acid Hydrazone Derivatives, Clive, D.L.J.; Zhang, J.; Subedi, R.; Bouétard, V.; Hiebert, S.; Ewanuk, R. J. Org. Chem. 2001, 66, 1233-1241 (DOI).
  138. Preparation of Polycyclic Systems by Sequential 5-Exo-Digonal Radical Cyclization, 1,5-Hydrogen Transfer from Silicon, and 5-EndoTrigonal Cyclization, Clive, D.L.J.; Yang, W.; MacDonald, A.; Wang, Z.; Cantin, M. J. Org. Chem. 2001, 66, 1966-1983 (DOI).
  139. A synthesis of puraquinonic acid, Hisaindee, S.; Clive, D.L.J. Tetrahedron Lett. 2001, 42, 2253-2255 (DOI).
  140. Tandem ring-closing metathesis-radical cyclization based on 4-(phenylseleno)butanal and methyl 3-(phenylseleno)propanoate –a route to bicyclic compounds, Clive, D.L.J.; Cheng, H. Chem. Commun. 2001, 605-606 (DOI).
  141. Stereocontrolled formation of spiro enones by radical cyclization of bromo acetals, Clive, D.L.J.; Huang, X. Tetrahedron 2001, 57, 3845-3858 (DOI).
  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, Chimie/Chemistry 2001, 4, 505-512 (DOI).
  143. Synthesis of (+)-Juruenolide C: Use of a Sequential 5-Exo-Diagonal Radical Cyclization, 1,5-lntramolecular Hydrogen Transfer, and 5-Endo-Trigonal Cyclization, Clive, D.L.J.; Ardelean, E.-S. J. Org. Chem. 2001, 66, 4841-4844 (DOI).
  144. Synthesis of Biaryls by lntramolecular Radical Transfer in Phosphinates, Clive, D.L.J., Kang, S. J. Org. Chem. 2001, 66, 6083-6091 (DOI).
  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. 2001, 42, 6267-6270 (DOI).
  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 2002, 28, 21-50.
  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. 2001, 67, 1192-1198 (DOI).
  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. 2002, 43, 4559-4563 (DOI).
  149. Synthesis of the bicyclic dienone core of the antitumor agent ottelione B, Clive, D.L.J.; Fletcher S.P. Chem. Commun. 2002, 1940-1941 (DOI).
  150. A Free Radical Method for Reduction of Cyclohexanones – Preferential Formation of Equatorial Alcohols, Clive, D.L.J.; Cheng, H. Synth. Commun. 2003, 33, 1951-1961 (DOI).
  151. Synthesis of (+)-puraquinonic acid, Clive, D.L.J.; Yu, M. Chem. Commun. 2002, 2380-2381 (DOI).
  152. Studies related to furopyridinone antibiotics, Synthesis of 2-epi-CJ-16,170, Clive, D.L.J.; Huang, X. Tetrahedron 2002, 58, 10243-10250 (DOI).
  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. Chem. Commun. 2003, 526-527 (DOI).
  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. Chem. 2003, 81, 811-824 (DOI).
  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. 2003, 42, 3406-3409 (DOI).
  156. First synthesis of the antifungal and antibacterial agent cladobotryal, Clive, D.L.J.; Huang, X. Chem. Commun. 2003, 2062-2063 (DOI).
  157. Derivatized Amino Acids Relevant to Native Peptide Synthesis by Chemical Ligation and Acyl Transfer, Clive, D.L.J.; Hisaindee, S.; Coltart, D.M. J. Org. Chem. 2003, 68, 9247-9254 (DOI).
  158. Synthesis of (+)-nocardione A – use of formal radical cyclization onto a benzene ring, Clive, D.L.J.; Fletcher, S.P. Chem. Commun. 2003, 2464-2465 (DOI).
  159. Synthesis of natural (–)-hamigeran B, Clive, D.L.J.; Wang, J. Tetrahedron Lett. 2003, 44, 7731-7733 (DOI).
  160. Model Studies and First Synthesis of the Antifungal and Antibacterial Agent Cladobotryal, Clive, D.L.J., Huang, X. J. Org. Chem. 2004, 69, 1872-1879 (DOI).
  161. Synthesis of (±)-Hamigeran B, (–)-Hamigeran B, and (±)-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon–Oxygen Bond from Hydrogenolysis, Clive, D.L.J., Wang, J. J. Org. Chem. 2004, 69, 2773-2784 (DOI).
  162. Formal Radical Cyclization onto Benzene Rings: A General Method and Its Use in the Synthesis of ent-Nocardione A, Clive, D.L.J., Fletcher, S.P., Liu, D. J. Org. Chem. 2004, 69, 3282-3293 (DOI).
  163. Synthesis of Optically Pure (+)-Puraquinonic Acid and Assignment of Absolute Configuration to Natural (–)-Puraquinonic Acid. Use of Radical Cyclization for Asymmetric Generation of a Quaternary Center, Clive, D.L.J., Yu, M., Sannigrahi, M. J. Org. Chem. 2004, 69, 4116-4125 (DOI).
  164. Synthesis of the substituted spiro segment of halichlorine – use of radical cyclization and stereospecific cuprate addition to an α,β-unsaturated lactam, Yu, M.; Clive, D.L.J.; Yeh, V.S.C.; Kang, S.; Wang, J. Tetrahedron Lett. 2004, 45, 2879-2881 (DOI).
  165. [2.2.2]-Bicyclic systems relevant to synthetic studies on CP-225,917 – use of a new silylated cyclopentadiene, Clive, D.L.J., Cheng, H., Gangopadhyay, P., Huang, X., Prabhudas, B. Tetrahedron 2004, 60, 4205-4221 (DOI).
  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. Chem. Commun. 2005, 906-908 (DOI).
  167. Oxidation of p-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. 2005, 7, 23-26 (DOI).
  168. Synthetic Chemistry of the Hamigerans. A Review, Clive, D.L.J.; Wang, J. Org. Prep. Proc. Int. 2005, 37, 3-35 (DOI).
  169. Conversion of Furans into γ-Hydroxybutenolides: Use of Sodium Chlorite, Clive, D.L.J.; Minarruzaman; Ou, L. J. Org. Chem. 2004, 70, 3318-3320 (DOI).
  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. 2005, 46, 2853-2855 (DOI).
  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. 2005, 105, 4483-4514 (DOI).
  172. A short synthetic route to the core structures of otteliones A and B, Clive, D.L.J.; Liu, D. Tetrahedron Lett. 2005, 46, 5305-5307 (DOI).
  173. Synthesis of the Core Structure of the Fungal Metabolite Benesudon: Use of Oxidative Decarboxylation, Clive, D.L.J.; Minaruzzaman; Yang, H. Org. Lett. 2005, 7, 5581-5583 (DOI).
  174. Carbocyclization by Radical Closure onto O-Trityl Oximes: Dramatic Effect of Diphenyl Diselenide, Clive, D.L.J.; Pham, M.P.; Subedi, R. J. Am. Chem. Soc. 2007, 129, 2713-2717 (DOI).
  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. 2007, 46, 3738-3740 (DOI).
  176. A convenient general method for the synthesis of hydroxy diacids, Chiruta, C.; Jachak, S.; Clive, D.L.J. Tetrahedron Lett. 2007, 48, 3141-3143 (DOI).
  177. Total synthesis of (–)-conocarpan and assignment of the absolute configuration by chemical methods, Clive, D.L.J.; Stoffman, E.J.L. Chem. Commun. 2007, 2151-2153 (DOI).
  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. 2007, 35, D521-D526 (DOI).
  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. 2007, 72, 5608-5617 (DOI).
  180. Formation of Benzo-Fused Carbocycles by Formal Radical Cyclization onto an Aromatic Ring, Clive, D.L.J.; Sunasee, R. Org. Lett. 2007, 9, 2677-2680 (DOI).
  181. Synthesis of Dihydrooxepin Models Related to the Antitumor Antibiotic MPC1001, Peng, J.; Clive, D.L.J. Org. Lett. 2007, 9, 2939-2941 (DOI).
  182. All-Carbon lntramolecular Conjugate Displacement Reactions: an Effective Route to Carbocycles, Prabhudas, B.; Clive, D.L.J. Angew. Chem. Int. Ed. 2007, 46, 9295-9297 (DOI).
  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. 2007, 9, 5315-5317 (DOI).
  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. J. Org. Chem. 2008, 73, 2330-2344 (DOI).
  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. J. Org. Chem. 2008, 73, 3078-3087 (DOI).
  186. Formal radical closure onto aromatic rings—a general route to carbocycles, Clive, D.L.J.; Sunasee, R.; Chen, Z. Org. Biomol. Chem. 2008, 6, 2434-2441 (DOI).
  187. Synthesis of (–)-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. 2008, 6, 1831-1842 (DOI).
  188. [1-(Phenylseleno)alkyl]stannanes—Mixed Selenium/Tin Analogs of Acetals: Preparation from α-Hydroxystannanes and Use for Generating Selenium-Stabilized Carbanions, Fernandopulle, S.C.; Clive, D.L.J.; Yu, M. J. Org. Chem. 2008, 73, 6018-6021 (DOI).
  189. The Naturally Occurring Ketene Acetal Benesudon: Total Synthesis and Assignment of Relative and Absolute Stereochemistry, Clive, D.L.J.; Minaruzzaman; Yang, H. J. Org. Chem. 2008, 73, 6743-6752 (DOI).
  190. A Route to 1,4-Disubstituted Aromatics and its Application to the Synthesis of the Antibiotic Culpin, Sunasee, R.; Clive, D.L.J. J. Org. Chem. 2008, 73, 8016-8020 (DOI).
  191. Asymmetric Synthesis of the ABC-Ring System of the Antitumor Antibiotic MPC1001, Peng, J.; Clive, D.L.J. J. Org. Chem. 2009, 74, 513-519 (DOI).
  192. Conversion of Weinreb Amides into Benzene Rings Incorporating the Amide Carbonyl Carbon, Clive, D.L.J.; Pham, M.P. J. Org. Chem. 2009, 74, 1685-1690 (DOI).
  193. Formation of Carbocycles by lntramolecular Conjugate Displacement: Scope and Mechanistic Insights, Wang, L.; Prabhudas, B.; Clive, D.L.J. J. Am. Chem. Soc. 2009, 131, 6003-6012 (DOI).
  194. The coumarin→indole Transformation—a method for preparing 4-halo-5-hydroxyindoles from coumarins, Stoffman, E.J.L.; Clive, D.L.J. Org. Biomol. Chem. 2009, 7, 4862-4870 (DOI).
  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. J. Org. Chem. 2009, 74, 7417-7428 (DOI).
  196. Desymmetrization of 4-hydroxy-2,5-cyclohexadienones by radical cyclization: synthesis of optically pure γ-lactones, Sunasee, R.; Clive, D.L.J. Chem. Commun. 2010, 46, 701-703 (DOI).
  197. Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine, Stoffman, E.J.; Clive, D.L.J. Tetrahedron 2010, 66, 4452-4461 (DOI).
  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. 2010, 75, 5223-5233 (DOI).
  199. Formation of Unusual Seven-Membered Heterocycles Incorporating Nitrogen and Sulfur by lntramolecular Conjugate Displacement, Chen, Z.; Clive, D.L.J. J. Org. Chem. 2010, 75, 7014-7017 (DOI).
  200. Conversion of 1,4-Diketones into para-Disubstituted Benzenes, Ziffle, V.E.; Cheng, P.; Clive, D.L.J. J. Org. Chem. 2010, 75, 8024-8038 (DOI).
  201. The [[(tert-Butyl)dimethylsilyl]oxy]methyl Group for Sulfur Protection, Wang, L.; Clive, D.L.J. Org. Lett. 2011, 13, 1734-1737 (DOI).
  202. The Marine Alkaloid Halichlorine: Its Defenses and its Defeat, Clive, D.L.J. In Strategies and Tactics in Organic Synthesis; Harmata, M., Ed.; Vol. 8, Academic Press: Burlington, 2012, pp. 25-54 (DOI).
  203. Synthetic studies related to MPC1001: formation of a model epidithiodiketopiperazine, Wang, L.; Clive, D.L.J. Tetrahedron Lett. 2012, 53, 1504-1506 (DOI).
  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. 2013, 90, 10-24 (DOI).
  205. Formation of Optically Pure Cyclic Amines by lntramolecular Conjugate Displacement, Cheng, P.; Clive, D.L.J. J. Org. Chem. 2012, 77, 3348-3364 (DOI).
  206. A Dieckmann Cyclization Route to Piperazine-2,5-diones, Aboussafy, C.L.; Clive, D.L.J. J. Org. Chem. 2012, 77, 5125-5131 (DOI).
  207. Racemic marinopyrrole B by total synthesis, Cheng, P.; Clive, D.L.J.; Fernandopulle, S.; Chen, Z. Chem. Commun. 2013, 49, 558-560 (DOI).
  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. 2013, 78, 996-1013 (DOI).
  209. Asymmetric synthesis of carbocycles: use of intramolecular conjugate displacement, Sreedharan, D.T.; Clive, D.L.J. Org. Biomol. Chem. 2013, 11, 3128-3144 (DOI).
  210. The marinopyrroles, Clive, D.L.J.; Cheng, P. Tetrahedron 2013, 69, 5067-5078 (DOI).
  211. A General Route of 1,3′-Bipyrroles, Cheng, P.; Shao, W.; Clive, D.L.J. J. Org. Chem. 2013, 78, 11866-11873 (DOI).
  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. 2015, 80, 3211-3216 (DOI).
  213. Synthesis of (+)-lpalbidine Based on 6-exo-trig Radical Cyclization of a β-Amino Radical, Chea, J.; Clive, D.L.J. J. Org. Chem. 2015, 80, 10294-10298 (DOI).
  214. A Family of Routes to Substituted Phenols, Including Meta-Substituted Phenols, Shao, W.; Clive, D.L.J. J. Org. Chem. 2015, 80, 12280-12287 (DOI).
  215. [(tert-Butyldi methylsilyl)oxy]methanethiol and [(tert-Butyldiphenylsilyl)oxy]methanethiol—nucleophilic protected H2S equivalents, Dong, S.; Clive, D.L.J.; Gao, J.-M. Tetrahedron Lett. 2015, 56, 6857-6859 (DOI).
  216. Conversion of cycloalk-2-enones into 2-methylcycloalkane-1,3-diones—assessment of various Tamao-Fleming procedures and mechanistic insight into the use of the Me3SiMe2Si unit, Yu, G.; Clive, D.L.J. Org. Biomol. Chem. 2016, 14, 1653-1664 (DOI).
  217. Computations Reveal That Electron-Withdrawing Leaving Groups Facilitate lntramolecular Conjugate Displacement Reactions by Negative Hyperconjugation, Noey, E.L.; Jiménez-Osés, G.; Clive, D.L.J.; Houk, K.N. J. Org. Chem. 2016, 81, 4290-4294 (DOI).
  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. 2016, 52, 8271-8274 (DOI).
  219. Formation of meta-Substituted Phenols by Transition Metal-Free Aromatization: Use of 2-Bromocyclohex-2-en-1-ones, Yu, G.; Clive, D.L.J. J. Org. Chem. 2016, 81, 8470-8484 (DOI).
  220. Formation of meta-arylsulfanyl- and meta-(alkylsulfanyl)phenols from cyclohexane-1,3-diones, Do, N.V.T.; Patra, S.; Clive, D.L.J. Tetrahedron 2018, 74, 4343-4350 (DOI).
  221. Synthesis of phenolic components of Grains of Paradise, Hattori, H.; Mitsunaga, T.; Clive, D.L.J. Tetrahedron Lett. 2019, 60, 1989-1991 (DOI).
  222. Formation of Enol Ethers by Radical Decarboxylation of α-Alkoxy β-Phenylthio Acids, Palanivel, A.; Mubeen, S.; Warner, T.; Ahmed, N.; Clive, D.L.J. J. Org. Chem. 2019, 84, 12542-12552 (DOI).
  223. Formation of 3-Aminophenols from Cyclohexane-1,3-diones, Szymor-Pietrzak, D.; Khan, M.N.; Pagès, A.; Kumar, A.; Depner, N.; Clive, D.L.J. J. Org. Chem. 2021, 86, 619-631 (DOI).
  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 2023, 133, 133264 (1-13) (DOI).

Patents

  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).
  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).
  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).
  4. Synthesis of (±)-calicheamicinone, precursors, intermediates and derivatives. Clive, D.L.J.; Daigneault, S.; Bo, Y.; Tao, Y. PCT WO 97/41109 (6 November, 1997).

Encyclopedia Articles

  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.
  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.
  3. Sodium O,O-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.
  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.
  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.
  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.
  7. Triphenylstannane, Clive, D.L.J. “Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley: New York, 1994; Vol. 8, 5412-5416.
  8. 2,2-Dimethyl-5-[3-(diphenylstannyl)propyl]-1,3-dioxolan-4-one. Wang, J.; Clive, D.L.J. “Electronic Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley:  New York, 2003. 
  9. Diphenyl[2-(4-pyridyl)ethyl]tin hydride.  Yang, W.; Clive, D.L.J. “Electronic Encyclopedia of Reagents for Organic Synthesis”; Paquette, L.A., Ed.; Wiley:  New York, 2003.
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