Publications

1. Chemistry of Tetracyclines, Clive, D.L.J. Quart. Rev. (London) 1968, 22, 435-456.

2. A New Method for Conversion of Aldoximes into Nitriles: Use of Chlorothionoformates, Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1970, 1014-1015.

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. Commun. 1971, 1112-1113.

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.

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.

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. Commun. 1972, 773-774.

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. Commun. 1973, 253.

8. Fragmentation of Selenoxides: a New Method for Dehydrogenation of Ketones, Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1973, 695-696.

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. Commun. 1974, 100.

10. Polyamide Supports for Polypeptide Synthesis, Atherton, E.; Clive, D.L.J.; Sheppard, R.C. J. Am. Chem. Soc. 1975, 97, 6584-6585.

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 11-17, 1976, pp. 291-297.

12. New Route to Bicyclic Lactones: Use of Benzeneselenenyl Chloride, Clive, D.L.J.; Chittattu, G. J. Chem. Soc., Chem. Commun. 1977, 484-485.

13. A new route to ring-fused tetrahydrofurans: reactions of Δ⁴-unsaturated alcohols with phenylselenenyl chloride, Clive, D.L.J.; Chittattu, G.; Wong, C.K. Can. J. Chem. 1977, 55, 3894-3897.

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. Commun. 1977, 657-658.

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. Commun. 1977, 658-659.

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. Commun. 1977, 725-727.

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. Commun. 1978, 41-42.

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. Commun. 1978, 379-380.

19. New Method of Access to Selenoacetal Chemistry: Use of Tris(Phenylseleno)borane, Clive, D.L.J.; Menchen, S.M. J. Chem. Soc., Chem. Commun. 1978, 356.

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. Commun. 1978, 441-442.

21. Modern Organoselenium Chemistry, Clive, D.L.J. Tetrahedron 1978, 34, 1049-1132.

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. Commun. 1978, 770-771.

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. Commun. 1979, 168-169.

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.

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.

27. Selenium and Tellurium Reagents for Organic Synthesis: 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.; Université 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.

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.

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.

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.

32. Generation of Carbon-Carbon Double Bonds from β-Oxygenated Phenylseleno, Phenylthio, and Iodo Species. A New Use for the Chlorotrimethylsilane-Sodium Iodide Reagent, Clive, D.L.J.; Kalè, V.N. J. Org. Chem. 1981, 46, 231-234.

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. Commun. 1981, 434-436.

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.

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. Commun. 1981, 643-644.

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.

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.

39. New Method for Coupling Allylic Halides: Use of Te^2- Species, Clive, D.L.J.; Anderson, P.C.; Moss, N.; Singh, A. J. Org. Chem. 1982, 47, 1641-1647.

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, 2572-2582.

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.

42. Formation of Carbon-Carbon Bonds by Ring Closure of b-Phenylselenocrotonates, Clive, D.L.J.; Beaulieu, P.L. J. Chem. Soc., Chem. Commun. 1983, 307-309.

43. Sapphyrins: Novel Aromatic Pentapyrrolic Macrocycles, Bauer, V.J.; Clive, D.L.J.; Dolphin, D.; Paine, J.B., III; Harris, F.L.; King, M.M.; Loder, J.; Wang, S.-W.C.; Woodward, R.B. J. Am. Chem. Soc. 1983, 105, 6429-6436.

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.

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.

46. Studies Related to Thromboxane A₂: A Formal Synthesis of Optically Active 9a,11a-Thiathromboxane A₂ Methyl Ester from Levoglucosan, Kalè, V.N.; Clive, D.L.J. J. Org. Chem. 1984, 49, 1554-1563.

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.

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.

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.

50. Radical Annulation: A Method for Preparation of Carbocycles, Angoh, A.G.; Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1985, 980-982.

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. J. Chem. Soc., Chem. Commun. 1985, 1205-1207.

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.

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.

54. Synthesis of Spiro-compounds Related to Fredericamycin A, Bennett, S.M.; Clive, D.L.J. J. Chem. Soc., Chem. Commun. 1986, 878-880.

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.

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.

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.

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.

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.

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.

61. Synthetic methodology involving radical cyclization: spiro compounds and α-oxo radicals, Clive, D.L.J. Pure Appl. Chem. 1988, 60, 1645-1654.

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.

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.

64. Conversion of Olefins into Five-membered Nitrogen Heterocycles by Radical Cyclization, Clive, D.L.J.; Mohammed, A.Y. Heterocycles 1989, 28, 1157-1167.

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.

66. Synthesis of (±)-Frullanolide: An Application of Radical Closure, Clive, D.L.J.; Joussef, A.C. J. Org. Chem. 1990, 55, 1096-1098.

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.

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.

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.

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.

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.

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. [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.

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.

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.

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.

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, S. J. Org. Chem. 1991, 56, 6447-6458. [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.

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.

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.

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.

83. Synthesis of Carbazomycin B, Clive, D.L.J.; Etkin, N.; Joseph, T.; Lown, J.W. J. Org. Chem. 1993, 58, 2442-2445.

84. trans Ring-fused Bicyclic Structures by 6-exo-Trigonal Radical Closure: Use of the Triethylborane-Stannane-Air System for Intramolecular Radical Addition to Aldehydes, Clive, D.L.J.; Postema, M.H.D. J. Chem. Soc., Chem. Commun. 1993, 429-430. [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.

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.

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.

88. Reaction of cis-Vicinal Dimesylates with Te^2-: 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.

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.

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. J. Chem. Soc., Chem. Commun. 1994, 235-236.

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.

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.

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.

    

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. Organometallic Chem. 1995, 489, C35-C37.

    

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.

    

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.

    

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.

    

98. A Nitrogen-Containing Stannane for Free Radical Chemistry, Clive, D.L.J.; Yang, W. J. Org. Chem. 1995, 60, 2607-2609.

    

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.

    

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.

     

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.

     

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.
     

     

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.

     

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.
     

     

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.

     

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.

     

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.

     

108. Formal synthesis of (-)-calicheamicinone and of (+)-calicheamicinone, Clive, D.L.J.; Selvakumar, N. J. Chem. Soc., Chem. Commun. 1996, 2543-2544.

     

109. Synthesis of the Aromatic Unit of Calicheamicin γ₁^I, Hu, Y.-Z.; Clive, D.L.J. J. Chem. Soc., Perkin Trans 1 1996, 1, 1421-1424.

     

110. Preaparation 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, J. J. Chem. Soc., Chem. Commun. 1997, 549-550.

     

111. Synthesis of 2',3'-Didehydro-2',3'-dideoxynucleosides by Reaction of 5'-O-Protected Nucleoside 2',3'-Dimesylates with Lithium Aryl Selenolates, Clive, D.L.J.; Sgarbi, P. W. M., Wickens, P. L. J. Org. Chem. 1997, 62, 3751-3753.

     

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.

     

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.

     

114. Synthesis of the Angiotensin-Converting Enzyme Inhibitor (±)-A58365A, Clive, D.L.J.; Coltart, D.M. Tetrahedron Lett. 1998, 39, 2519-2522.

     

115. A synthetic route from D-glucose to D-myo-inositol-1,4,5-tris(dihydrogenphosphate): use of an unusual ene reaction, Clive, D.L.J.; Xiao He, Postema, M.H.D.; Mashimbye, J. Tetrahedron Lett. 1998, 39, 4231-4234.

     

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.

     

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.

     

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.

     

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.

     

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.

     

121. Synthesis of (+)-Furanomycin: Use of Radical Cyclization, Clive, D. L. J.; Zhang, J. J. Org. Chem. 1999, 64, 1754-1757.

     

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.

     

123. Formal Synthesis of D-Myo-Inositol-1,4,5-tris(dihydrogen phosphate): Cyclization by an Unusual Ene Reaction and Use of the Bu₂SnCl₂/Bu₂SnH₂ 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.

     

124. Studies on the Preparation of 3,4-Disubstituted 2-Methoxypyridines, Pelisson, M.M.M.; da Silva, G.V.; Clive, D.L.J.; Coltart, D.M.; Hof, F.A. J. Heterocyclic Chem. 1999, 36, 653-658.
     

     

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.

     

126. Model Studies related to CP-225,917: Stereocontrolled Generation of the Quaternary Center, Clive, D.L.J.; Zhang, J. Tetrahedron 1999, 41, 12059-12068.

     

127. Synthesis of Racemic Brevioxime, Clive, D.L.J.; Hisaindee, S. Chem. Commun. 1999, 2251-2252.

     

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.

     

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.

     

130. Synthesis of Biaryls by Intramolecular Radical Transfer, Clive, D.L.J.; Kang, S. Tetrahedron Lett. 2000, 41, 1315-1319.

     

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.

     

132. Synthesis of Racemic Brevioxime and Related Model Compounds, Clive, D.L.J.; Hisaindee, S.J. Org. Chem. 2000, 65, 4923-4929.

     

133. Synthetic Studies on Calicheamicin γ₁^I - 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.
     

     

134. An Approach to the Anhydride Unit of CP-225,917 and CP-263,114, Clive, D.L.J.; Sun, S.; and (in part) Gagliardini, V.; Sano, M.K. Tetrahedron Lett. 2000, 41, 6259-6263.

     

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.; 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.

     

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.

     

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.
     

     

138. Preparation of Polycyclic 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.; MacDonald, A.; Wang, Z.; Cantin, M. J. Org. Chem. 2001, 66, 1966-1983.

     

139. A Synthesis of Puraquinonic Acid, Hisaindee, S.; Clive, D.L.J. Tetrahedron Lett. 2001, 42, 2253-2255.

     

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.

     

141. Stereocontrolled Formation of Spiro Enones by Radical Cyclization of Bromo Acetals, Clive, D.L.J.; Huang, X. Tetrahedron 2001, 57, 3845-3858.

     

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.
     

     

143. Synthesis of (+)-Juruenolide C — Use of a Sequential 5-Exo-Diagonal Radical Cyclization, 1,5-Intramolecular Hydrogen Transfer, and 5-Endo-Trigonal Cyclization, Clive, D.L.J.; Ardelean, E.-S., J. Org. Chem. 2001, 66, 4841-4844.
     

     

144. Synthesis of Biaryls by Intramolecular Radical Transfer in Phosphinates, Clive, D.L.J., Kang, S. J. Org. Chem. 2001, 66, 6083-6091.

     

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.

     

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 Actualité de Chimie Thérapeutique; 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.

     

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.

     

149. Synthesis of the Bicyclic Core of the Antitumor Agent Ottelione B, Clive, D.L.J.; Fletcher, S.P. J. Chem. Soc., Chem. Commun. 2002, 1940-1941.

     

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.

     

151. Synthesis of (+)-Puraquinonic Acid, Clive, D.L.J.; Yu, M. J. Chem. Soc., Chem. Commun. 2002, 2380-2381.

     

152. Studies Related to Furopyridinone Antibiotics, Clive, D.L.J.; Huang, X. Tetrahedron 2002, 58, 10243-10250.

     

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. J. Chem. Soc., Chem. Commun. 2003, 526-527.
     

     

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.

     

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. Edn. 2003, 42, 3406-3409.

     

156. First Synthesis of the Antifungal and Antibacterial Agent Cladobotryal, Clive, D.L.J.; Huang, X. J. Chem. Soc., Chem. Commun. 2003, 2062-2063.

     

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.

     

158. Synthesis of (+)-Nocardione A — Use of Formal Radical Cyclization onto a Benzene Ring, Clive, D.L.J.; Fletcher, S.P. J. Chem. Soc., Chem. Commun. 2003, 2464-2465.

     

159. Synthesis of Natural (-)-Hamigeran B, Clive, D.L.J.; Wang, J. Tetrahedron Lett. 2003, 44, 7731-7733.

     

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.

     

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.

     

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, 3282-3293.

     

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.

     

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.

     

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.

     

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. J. Chem. Soc., Chem. Commun. 2005, 906-908.

     

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.

     

168. Synthetic Chemistry of the Hamigerans. Clive, D.L.J.; Wang, J. Org. Prep. Proc. Int. 2005, 37, 3-35.

     

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.

     

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.
     

     

171. Synthetic Chemistry of Halichlorine and the Pinnaic Acid. Clive, D.L.J.; Yu, M.; Wang, J.; Yeh, V.S.C.; Kang, S. Chem. Rev. 2005, 105, 4483-4514.

     

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.

     

173. Synthesis of the Core of the Fungal Metabolite Benesudon — Use of Oxidative Decarboxylation. Clive, D.L.J.; Minaruzzaman; Yang, H. Org. Lett., 2005, 7, 5581-5583.

     

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.

     

175. A convenient general method for the synthesis of hydroxy diacids.  Chiruta, C.; Jachak, S.; Clive, D.L.J. Tetrahedron Lett. 2007, 48, 3141-3143.

     

176. Synthesis of 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.

     

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.

     

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. and Querengesser, L. Nucleic Acids Res. 2007, 35, D521-D526.

179. Intramolecular 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. J. Org. Chem. 2007, 72, 5608-5617.

     

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.

     

181. Synthesis of Dihydrooxepin Models Related to the Antitumor Antibiotic MPC1001.  Peng, J.; Clive, D.L.J. Org. Lett. 2007, 9, 2939-2941.

     

182. All-Carbon Intramolecular Conjugate Displacement (ICD) Reactions – an Effective Route to Carbocycles.  Prabhudas, B.; Clive, D.L.J.  Angew. Chem. Int. Ed. 2007, 46, 9295-9297.

     

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.

     

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.&

     

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.

     

186. 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.

     

187. 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.

     

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.

     

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.

     

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.

     

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.

     

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.

     

193. Generation of Carbocycles by Intramolecular Conjugate Displacement:  Scope and Mechanistic Insights.  Wang, L.; Prabhudas, B.; Clive, D.L.J.  J. Am. Chem. Soc. 2009, 131, 6003-6012.

     

194. The Coumarin to 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.

     

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.

     

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.&

     

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.

     

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.

     

199. Formation of Unusual Seven-Membered Heterocycles Incorporating Nitrogen and Sulfur by Intramolecular Conjugate Displacement.  Chen, Z.; Clive, D.L.J. J. Org. Chem. 2010, 75, 7014-7017.

     

200. Conversion of 1,4-Diketones into p-Disubstituted Benzenes.  Ziffle, V. E.; Cheng, P.; Clive, D.L.J. J. Org. Chem. 2010, 75, 8024-8038.

     

201. The [[(tert-Butyl)dimethylsilyl]oxy]methyl Group for Sulfur Protection.  Wang, L.; Clive, D.L.J. Org. Lett. 2011, 13, 1734-1737.

     

202. Synthetic studies related to MPC1001: formation of a model epidithiodiketopiperazine. Wang, L.; Clive, D.L.J. Tetrahedron Lett. 2012, 53, 1504-1506.

     

203. Formation of Optically Pure Cyclic Amines by Intramolecular Conjugate Displacement. Cheng, P.; Clive, D.L.J. J. Org. Chem. 2012, 77, 3348-3364.

     

204. A Dieckmann Cyclization Route to Piperazine-2,5-diones. Larrivée Aboussafy, C.; Clive, D.L.J. J. Org. Chem. 2012, 77, 5125-5131.

     

205. 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.

     

206. 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.

     

207. Racemic Marinopyrrole B by Total Synthesis. Cheng, P.; Clive, D.L.J.; Fernandopulle, S.; Chen, Z. Chem. Commun. 2013, 49, 558-560.

     

208. Synthetic Studies on CP-225,917 and CP-263,114: Access to Advanced Tetracyclic Systems by Intramolecular Conjugate Displacement and [2,3]-Wittig Rearrangement. Malihi, F.; Clive, D.L.J.; Chang, C.-C.; Minaruzzaman J. Org. Chem. 2013, 78, 996-1013.

     

209. Asymmetric synthesis of carbocycles: use of intramolecular conjugate displacement. Sreedharan, D.T.; Clive, D.L.J. Org. Biomol. Chem. 2013, 11, 3128-3144.

     

210. The Marinopyrroles. Clive, D.L.J.; Cheng, P. Tetrahedron 2013, 69, 5067-5078.

     

211. A General Synthesis of 1,3'-Bipyrroles. Cheng, P.; Shao, W.; Clive, D.L.J. J. Org. Chem. 2013, 78, 11866-11873.

     

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.

     

213. Synthesis of (+)-Ipalbidine 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.

     

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.

     

215. [(tert-Butyldimethylsilyl)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.

     

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, 17, 1653-1664.

     

217. Computations Reveal That Electron-Withdrawing Leaving Groups Facilitate Intramolecular Conjugate Displacement Reactions by Negative Hyperconjugation. Noey, E. L.; Jimènez-Osès, G.; Clive, D. L. J.; Houk, K. N. J. Org. Chem. 2016, 81, 4290-4294.

     

218. Synthesis of Models of the BC Ring Systems of MPC1001 and MPC1001F. Dong, S.; Indukuri, K.; Clive, D. L. J.; Gao, J.-M. Chem. Commun. 2016, 52, 8271-8274.

     

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.

     

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.

     

221. Synthesis of phenolic components of Grains of Paradise. Hattori, H.; Mitsunaga, T.; Clive, D. L. J. Tetrahedron Lett. 2019, 60, 1989-1991.

     

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.

     

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.

     

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).

     

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).

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.