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Volumn 153-154, Issue , 1999, Pages 79-97

New aspects of the thio-Wittig-reaction

Author keywords

Selenoketones; Staudinger chalcogenation; Thiaphosphetanes thia betaines

Indexed keywords


EID: 4244055876     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426509908546428     Document Type: Article
Times cited : (3)

References (77)
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    • 0000861506 scopus 로고
    • edited by D. R. Hogg The Chemical Society: London
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1977) Organic Compounds of Sulfur, Selenium, and Tellurium , vol.4 , pp. 124
    • Metzner, P.1    Hogg, D.R.2    Walter, W.3    Voss, J.4
  • 4
    • 0001260781 scopus 로고
    • edited by D. Klamann Georg Thieme, New York, Bd. E
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1985) Houben-Weyl, Methoden der Organischen Chemie , vol.11 , pp. 188
    • Voss, J.1
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    • edited by J. E. Baldwin Pergamon, Oxford
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1986) Selenium Reagents and Intermediates in Organic Synthesis , pp. 58
    • Paulmier, C.1
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    • 0002464379 scopus 로고
    • edited by S. Patai and Z. Rappoport Wiley, New York
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1986) The Chemistry of Organic Selenium and Tellurium Compounds , vol.1 , pp. 1
    • Jensen, K.A.1    Kjaer, A.2
  • 7
    • 0001284246 scopus 로고
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1987) The Chemistry of Organic Selenium and Tellurium Compounds , vol.2 , pp. 215
    • Guziec F.S., Jr.1
  • 8
    • 0002106278 scopus 로고
    • edited by D. Liotta Wiley, New York
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1987) Organoselenium Chemistry , pp. 277
    • Guziec F.S., Jr.1
  • 9
    • 84951813737 scopus 로고
    • The thiocarbonyl group
    • edited by S. Patai Wiley, New York
    • See e.g.: P. Metzner, D. R. Hogg, W. Walter, and J. Voss, in Organic Compounds of Sulfur, Selenium, and Tellurium: edited by D. R. Hogg (The Chemical Society: London, 1977), Vol. 4, p. 124. J. Voss, in Houben-Weyl, Methoden der Organischen Chemie; edited by D. Klamann (Georg Thieme, New York, 1985), Bd. E 11, p. 188. C. Paulmier, in Selenium Reagents and Intermediates in Organic Synthesis; edited by J. E. Baldwin (Pergamon, Oxford, 1986), p. 58. K. A. Jensen and A. Kjaer, in The Chemistry of Organic Selenium and Tellurium Compounds; edited by S. Patai and Z. Rappoport (Wiley, New York, 1986), Vol. 1, p. 1. F. S. Guziec, Jr., in The Chemistry of Organic Selenium and Tellurium Compounds; 1987, Vol. 2, p. 215. F. S. Guziec, Jr., in Organoselenium Chemistry, edited by D. Liotta (Wiley, New York, 1987), p. 277. E. Schaumann, in The Thiocarbonyl Group; in The Chemistry of Double-bonded Functional Groups, edited by S. Patai (Wiley, New York, 1989). Vol. 2, p. 1269.
    • (1989) The Chemistry of Double-bonded Functional Groups , vol.2 , pp. 1269
    • Schaumann, E.1
  • 10
    • 37049125143 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1975) J. Chem. Soc., Chem. Commun. , pp. 539
    • Back, T.G.1    Barton, D.H.R.2    Britten-Keley, M.R.3    Guziec F.S., Jr.4
  • 11
    • 0009418460 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1976) J. Chem. Soc., Perkin Trans I , pp. 2079
  • 12
    • 33845557603 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 7055
    • Cullen, E.R.1    Guziec F.S., Jr.2    Murphy, C.J.3    Wong, T.C.4    Andersen, K.K.5
  • 13
    • 0009373946 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1982) J. Chem. Soc., Perkin Trans 2 , pp. 473
  • 14
    • 0000752548 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1988) Bull. Chem. Soc. Jpn. , vol.61 , pp. 861
    • Ishii, A.1    Okazaki, R.2    Inamoto, N.3
  • 15
    • 33845184037 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 5949
    • Okazaki, R.1    Kumon, N.2    Inamoto, N.3
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    • 0002813388 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1986) J. Chem. Soc., Chem. Commun. , pp. 1152
    • Kirby, G.W.1    Tretheway, A.N.2
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    • 0009443989 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1988) J. Chem. Soc., Perkin Trans I , pp. 1933
  • 18
    • 33845374240 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 1314
    • Krafft, G.A.1    Meinke, P.T.2
  • 19
    • 0009319071 scopus 로고
    • For selected examples see e.g.: T. G. Back, D. H. R. Barton, M. R. Britten-Keley, and F. S. Guziec, Jr., J. Chem. Soc., Chem. Commun., 539 (1975); J. Chem. Soc., Perkin Trans I, 2079 (1976). E. R. Cullen, F. S. Guziec, Jr., C. J. Murphy, T. C. Wong, and K. K. Andersen, J. Am. Chem. Soc., 103, 7055 (1981); J. Chem. Soc., Perkin Trans 2, 473 (1982). A. Ishii, R. Okazaki, and N. Inamoto, Bull. Chem. Soc. Jpn., 61, 861 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. Soc., 111, 5949 (1989). G. W. Kirby and A. N. Tretheway, J. Chem. Soc., Chem. Commun., 1152 (1986); J. Chem. Soc., Perkin Trans I, 1933 (1988). G. A. Krafft and P. T. Meinke, J. Am. Chem. Soc., 108, 1314 (1986); Tetrahedron Lett., 28, 5121 (1987) ; J. Am. Chem. Soc., 110, 8671, 8679 (1988). M. Segi, T. Nakajima, S. Suga, S. Murai, I. Ryn, A. Ogawa, and N. Sonoda, J. Am. Chem. Soc., 110, 1976 (1988). R. Okazaki, N. Kumon, and N. Inamoto, J. Am. Chem. S, 111, 5949 (1989). M. Minoura, T. Kawashima, and R. Okazaki, J. Am. Chem. Soc., 115, 7019 (1993).
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5121
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