Highly efficient synthesis of chiral β-hydroxy sulfides with high enantiomeric purity via CBS-oxazaborolidine-catalyzed borane reduction
摘要:
A simple and efficient synthesis of chiral beta-hydroxy p-tolylsulfides with high enantiomeric purity by CBS-oxazaborolidine-catalyzed asymmetric borane reduction of beta-keto p-tolyisulfides using N-ethyl-N-isopropylaniline-borane complex as the borane carrier is reported. (C) 2002 Elsevier Science Ltd. All rights reserved.
Arora, Kanwar J. S.; Collier, John R.; Deodhar, Dinker J., Journal of Chemical Research, Miniprint, 1985, # 6, p. 2148 - 2183
作者:Arora, Kanwar J. S.、Collier, John R.、Deodhar, Dinker J.、Hesabi, Masoud-M.、Hill, John
DOI:——
日期:——
Highly efficient synthesis of chiral β-hydroxy sulfides with high enantiomeric purity via CBS-oxazaborolidine-catalyzed borane reduction
作者:Byung Tae Cho、Ok Kyoung Choi、Dong Jun Kim
DOI:10.1016/s0957-4166(02)00193-3
日期:2002.5
A simple and efficient synthesis of chiral beta-hydroxy p-tolylsulfides with high enantiomeric purity by CBS-oxazaborolidine-catalyzed asymmetric borane reduction of beta-keto p-tolyisulfides using N-ethyl-N-isopropylaniline-borane complex as the borane carrier is reported. (C) 2002 Elsevier Science Ltd. All rights reserved.