Asymmetric organic catalysis with modified cinchona alkaloids
摘要：
Insights into the role played by modified cinchona alkaloids in the Sharpless asymmetric dihydroxylation inspired studies of modified cinchona alkaloids as chiral organic catalysts that lead to the development of highly enantioselective alcoholyses for the desymmetrization, kinetic resolution, and dynamic kinetic resolution of cyclic anhydrides, cyanation of ketones, and 1,4-addition of thiols to cylic enones. These studies demonstrate the potential of modified cinchona alkaloids as broadly useful chiral organic catalysts for asymmetric synthesis.
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关键词：
organic chemistry, review diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism
DOI：
10.1021/ar030048s
被引量：
年份：
2004
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