Orientational effects in ring-opening reactions of some unsymmetrically substituted episulfides
NV Schwartz
Index: Schwartz,N.V. Journal of Organic Chemistry, 1968 , vol. 33, # 7 p. 2895 - 2902
Full Text: HTML
Citation Number: 28
Abstract
The reactions of propylene sulfide, isobutylene sulfide, and chloropropylene sulfide with hydrogen chloride] acetyl chloride, and anhydrous chlorine have been found, contrary to earlier reports, to yield mixtures of isomeric products resulting from ring opening at both CS bonds. Propylene sulfide was treated with a number of other electrophilic reagents such as hydrogen bromide, acetyl bromide, bromine, acetic anhydride, and benzoyl chloride. In each case, mixtures ...
Related Articles:
[Bordwell; Andersen Journal of the American Chemical Society, 1953 , vol. 75, p. 4959,4961]
[Robinson, Philip L.; Kelly, Jeffery W.; Slayton, A. Evans Phosphorus and Sulfur and the Related Elements, 1987 , vol. 31, p. 59 - 70]
[Prochazka,M.; Durdovic,P. Collection of Czechoslovak Chemical Communications, 1977 , vol. 42, p. 2401 - 2407]