Preparation of Optically Active Pyrrol-2-ylmethanols by Kinetic Resolution Using the Modified Sharpless Asymmetric Epoxidation Reagent
Kinetic resolution of pyrrol-2-ylmethanols was carried out by using the modified Sharpless asymmetric epoxidation reagent to give the slow-reaction enantiomers (R)-3a-g and (S)-3b,d with high enantioselectivity (>90percent e.e.) and high chemical yield (30 - 43percent)
Zhou, Wei-Shan,Wei, Dong
p. 1971 - 1980
(2007/10/02)
Preparation of Optically Active α-Pyrryl Carbinols by Kinetic Resolution Using the Modified Sharpless Asymmetric Epoxidation Reagent
Kinetic resolution of α-pyrryl carbinol was carried out by using the modified Sharpless asymmetric epoxidation reagent to give the slow-reacting enantiomers, (R)-3a-f and (S)-3b,d in high enantioselectivity (>90percent e.e.) and high chemical yield (30-43
Zhou, Wei-Shan,Wei, Dong
p. 767 - 770
(2007/10/02)
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