Efficient formation of aromatic thiols from thiomethylated precursors

Tetrahedron Letters

Volumn 40, Issue 30, 1999, Pages 5479-5482

  Pinchart, Alain ^a   Dallaire, Carol ^a   Van Bierbeek, Alain ^a   Gingras, Marc ^a  

^a UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUND; METHYL GROUP; THIOL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DEMETHYLATION; REACTION ANALYSIS; SYNTHESIS; TEMPERATURE SENSITIVITY;

EID: 0033166246     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01052-7     Document Type: Article

References (8)

1. Metzner, P.: Thuillier, A. Sulfur Reagents in Organic Synthesis; Academic Press: London, 1994, pp. 3-6.
2. Recent reviews: a) Baird, C. P.; Rayner, C. M. J. Chem. Soc. Perkin Trans. 1, 1998, 1973-1975;
3. b) Taylor, P. C. Comprehensive Organic Functional Group Transformation: Katritzky, A. R.; Meth-Cohn, O.; Rees, C. W.; Ley, S. V. Eds; Pergamon Press, London, 1995, Vol. 2, pp. 705-708.
4. a) Pinchart, A.; Dallaire, C.; Gingras, M. Tetrahedron Lett. 1998, 39, 543-546;
5. b) The Pummerer reaction is a high yielding method but several steps are required: Young, R. N.; Gauthier, J. Y.: Coombs, W. Tetrahedron Lett. 1984, 25, 1753-1756.
6. MeSNa: a) Testaferri, L.; Tingoli, M.: Tiecco, M. Tetrahedron Lett. 1980, 21, 3099-3100;
7. b) Testaferri, L.; Tiecco, M.; Tingoli, M.; Chianelli, D.; Montanucci, M. Synthesis 1983, 751-755. nPrSNa: Shaw, J. E. J. Org. Chem. 1991, 56, 3728.
8. b) Testaferri, L.; Tiecco, M.; Tingoli, M.;Chianelli, D.; Montanucci, M. Synthesis 1983, 751-755. nPrSNa: Shaw, J. E. J. Org. Chem. 1991, 56, 3728.