Control of diastereofacial selectivity in the nucleophilic epoxidation of γ-oxygenated-α,β-unsaturated sulphones
摘要:
Epoxidation of gamma-oxygenated-alpha,beta-unsaturated sulphones 4-8 with lithium t-butyl hydroperoxide proceeds with moderate to high diastereoselectivity to give 2-phenylsulphonyl oxiranes 9-13. The sense of diastereoselectivity is dependent on the steric bulk of the alkyl substituent at the gamma-centre.
MAHLER, HELLMUT;BRAUN, MANFRED, CHEM. BER., 124,(1991) N, C. 1379-1395
作者:MAHLER, HELLMUT、BRAUN, MANFRED
DOI:——
日期:——
Control of diastereofacial selectivity in the nucleophilic epoxidation of γ-oxygenated-α,β-unsaturated sulphones
作者:Richard F.W. Jackson、Stephen P. Standen、William Clegg
DOI:10.1016/s0040-4039(00)92395-5
日期:1991.9
Epoxidation of gamma-oxygenated-alpha,beta-unsaturated sulphones 4-8 with lithium t-butyl hydroperoxide proceeds with moderate to high diastereoselectivity to give 2-phenylsulphonyl oxiranes 9-13. The sense of diastereoselectivity is dependent on the steric bulk of the alkyl substituent at the gamma-centre.