Preparation of α-Halovinyl Sulfides by Eliminative Deoxygenation of α-Halosulfoxides
RD Miller, R Hässig
Index: Moller, R. D.; Haessig, R. Synthetic Communications, 1984 , vol. 14, # 14 p. 1285 - 1290
Full Text: HTML
Citation Number: 9
Abstract
Abstract Vinyl sulfides are useful synthetic intermediates1 which have received increasing attention recently both as masked carbonyl moieties2 and in carbon-carbon bond forming reactions. 3 With regard to the latter, vinyl sulfide derivatives which are substituted in the α- position with halogen, tin, selenium, etc., are particularly useful due to the ready formation of anions upon treatment with a variety of organometallic reagents. 3 d− 1 We report here ...
Related Articles:
Synthesis of 1, 1-disubstituted ethenes by means of sequential cross-coupling reactions
[Fiandanese, V.; Marchese, G.; Naso, F.; Ronzini, L. Synthesis, 1987 , # 11 p. 1034 - 1036]