The Versatile Phenylthio Group. A Powerful Aid in Synthesis

References

• Cohen , T. and Bhupathy , M. 1989 . Acc. Chem. Res. , 22 : 152
   Google Scholar
• Cohen , T. 1990 . Heteroatom Chemistry , Edited by: Block , E. New York : VCH Publishers . Chapter 7
   Google Scholar
• Screttas , C. G. and Micha-Screttas , M. 1978 . J. Org. Chem. , 43 : 1064
   Web of Science ®Google Scholar
• Cohen , T. , Daniewski , W. M. and Weisenfeld , R. B. 1978 . Tetrahedron Lett. , : 4665
   Google Scholar
• Cohen , T. , Herman , G. , Falck , J. R. and Mura , A. R. Jr . 1975 . J. Org. Chem. , 40 : 812
   Google Scholar
• Cohen , T. , Kuhn , D. and Falck , J. R. 1975 . J. Am. Chem. Soc , 97 : 4749
   Google Scholar
• Durst , T. 1984 . Comprehensive Carbanion Chemistry. Part B , Edited by: Buncel , E. and Durst , T. New York : Elsevier . Chapter 5
   Google Scholar
• Cohen , T. and Doubleday , M. D. 1990 . J. Org. Chem. , 55 : 4784
   Google Scholar
• Cohen , T. and Matz , J. R. 1980 . Synth. Commun. , 10 : 311
   Web of Science ®Google Scholar
• Bank , S. and Platz , M. 1973 . Tetrahedron Lett. , : 2097 The sodium analogue was known
   Google Scholar
• Freeman , P. K. and Hutchinson , L. L. 1980 . J. Org. Chem. , 45 : 1924
   Google Scholar
• 1983 . 48 : 4705
   Google Scholar
• Cohen , T. and Matz , J. R. 1980 . J. Am. Chem. Soc. , 102 : 6900
   Web of Science ®Google Scholar
• Schöllkopf , U. 1970 . Methoden der Organischen Chemie, , 4th ed. , Edited by: Müller , E. Vol. 13 , 133 87 Stuttgart : Houben-Weyl, Georg Theime Verlag . Footnote 8 Part 1
   Google Scholar
• Peterson , D. 1972 . J. Organomet. Chem. Rev., Sect. , A 7 : 295
   Google Scholar
• Still , W. C. 1978 . J. Am. Chem. Soc. , 100 : 1481
   Web of Science ®Google Scholar
• Still , W. C. and Mitra , A. 1978 . Ibid. , 100 : 1927
   Google Scholar
• Seebach , D. and Meyer , N. 1976 . Angew. Chem. Int. Ed. Engl , 15 : 438 See also
   Google Scholar
• Sawyer , J. S. , Kucerovy , A. , Macdonald , T. L. and McGarvey , G. J. 1988 . J. Am. Chem. Soc. , 110 : 842 They have since been prepared by tin-lithium exchange, albeit in considerably lower overall yield
   Google Scholar
• Cohen , T. and Lin , M.-T. 1984 . J. Am. Chem. Soc. , 106 : 1130
   Google Scholar
• Lancelin , J.-M. , Morin-Allory , L. and Sinay , P. 1984 . J. Chem. Soc., Chem, Commun. , 355
   Google Scholar
• Verner , E. and Cohen , T. 1992 . J. Am. Chem. Soc. , 114 : 375
   Google Scholar
• Verner , E. and Cohen , T. 1992 . J. Org. Chem. , 57 : 1072
   Google Scholar
• Cohen , T. and Guo , B.-S. 1986 . Tetrahedron , 42 : 2803
   Google Scholar
• Guo , B. S. , Doubleday , W. and Cohen , T. 1987 . J. Am. Chem. Soc. , 109 : 4710
   Google Scholar
• Cabral , J. A. , Cohen , T. , Doubleday , W. W. , Duchelle , E. F. , Fraenkel , G. , Guo , B.-S and Yü , S. H. J. Org. Chem. , in press
   Google Scholar
• Nakagawa , I. and Hata , T. 1975 . Tetrahedron Lett. , 1409
   Google Scholar
• Mukaiyama , T. , Matsueda , R. and Suzuki , M. 1970 . Tetrahedron Lett. , 1901
   Google Scholar
• Schlosser , M. , Hartmann , J. and David , V. 1974 . Helv. Chim. Acta , 57 : 1567
   Google Scholar
• Bates , R. B. and Beavers , W. A. 1974 . J. Am. Chem. Soc. , 96 : 5001
   Google Scholar
• Houk , K. N. , Strozier , R. W. , Rondan , N. G. , Fraser , R. R. and Chauqui-Offermanns , W. 1980 . J. Am. Chem. Soc. , 102 : 1426
   Google Scholar
• Reference 15 and citations therein
   Google Scholar
• Abraham , W. D. and Cohen , T. 1991 . J. Am. Chem. Soc. , 113 : 2314
   Google Scholar
• McCullough , D. W. , Bhupathy , M. , Piccolino , E. and Cohen , T. 1991 . Tetrahedron , 42 : 9727
   Google Scholar
• Moore , R. E. 1977 . Acc. Chem. Res. , 10 : 40
   Web of Science ®Google Scholar
• Cherkauskas , J. P. and Cohen , T. 1992 . J. Org. Chem. , 57 : 6
   Web of Science ®Google Scholar
• Kuwajima , I. and Nakamura , E. 1990 . Topics in Current Chemistry , 155 : 11 Reviews of homoenolate equivalents
   Google Scholar
• Hoppe , D. 1984 . Angew. Chem. Int. Ed. Engl. , 23 : 932
   Google Scholar
• Stowell , J. C. 1984 . Chem. Rev. , 84 : 409
   Web of Science ®Google Scholar
• Werstiuk , N. H. 1983 . Tetrahedron , 39 : 205
   Google Scholar
• Paterson , I. and Fleming , I. 1979 . Tetrahedron Lett. , 995
   Google Scholar
• Paterson , I. 1988 . Tetrahedron , 44 : 4207
   Google Scholar
• Posner , G. H. , Whitten , C. E. and Sterling , J. J. 1973 . J. Am. Chem. Soc. , 95 : 7788
   Web of Science ®Google Scholar
• Cherkauskas , J. P. , Zhang , B. and Cohen , T. unpublished work
   Google Scholar
• Ramón , D. J. and Yus , M. 1991 . J. Org. Chem. , 56 : 3825 For a method of producing the primary organolithium analogues, see
   Google Scholar
• Mudryk , B. , Shook , C. A. and Cohen , T. 1990 . J. Am. Chem. Soc. , 112 : 6389
   Google Scholar
• Boivin , T. L. B. 1987 . Tetrahedron , 43 : 3309
   Web of Science ®Google Scholar
• Mudryk , B. and Cohen , T. 1991 . J. Org. Chem. , 56 : 5760
   Web of Science ®Google Scholar
• Grovenstein , E. J. 1978 . Angew. Chem., Int. Ed. Engl. , 17 : 313 A review of some earlier examples
   Google Scholar
• Maercker , A. , Bsata , M. , Buchmeier , W. and Engelen , B. 1984 . Chem. Ber. , 117 : 2547 For an apparent exception in a system with a special driving force, see
   Google Scholar
• Mudryk , B. and Cohen , T. unpublished results
   Google Scholar
• Rychnovsky , S. C. 1989 . J. Org. Chem. , 54 : 4982 Rychnovsky had shown that organolithiums are far less destructive of THE when the latter is diluted with a substantial amount of hexane
   Google Scholar
• Cohen , T. and Myers , M. 1988 . J. Org. Chem. , 53 : 458
   Google Scholar
• Cohen , T. , Jung , S.-H. , Romberger , M. L. and McCullough , D. W. 1988 . Tetrahedron Lett. , 29 : 25
   Web of Science ®Google Scholar
• Shook , C. A. and Cohen , T. unpublished results
   Google Scholar
• Sherbine , J. P. 1985 . Ph. D. Thesis University of Pittsburgh .
   Google Scholar
• Romberger , M. L. 1989 . Ph. D. Thesis University of Pittsburgh .
   Google Scholar
• Jung , S.-H. , Xiao , M. and Cohen , T. unpublished results
   Google Scholar