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Asymmetric total synthesis of (+)-1-deoxy-6-epi-castanospermine

Asymmetric total synthesis of (+)-1-deoxy-6-epi-castanospermine
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摘要 (+)-l-Deoxy-6-epi-castanospermine was asymmetrically synthesized in ten steps from a-furfuryl amine derivative 6 in 2.9% overall yield. The kinetic resolution of a-furfuryl mine derivative 6 and Sharpless AD reaction of 14 were used as key steps. (+)-l-Deoxy-6-epi-castanospermine was asymmetrically synthesized in ten steps from a-furfuryl amine derivative 6 in 2.9% overall yield. The kinetic resolution of a-furfuryl mine derivative 6 and Sharpless AD reaction of 14 were used as key steps.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1998年第1期34-44,共11页 中国化学(英文版)
基金 Project (29732061) supported by the National Natural Science Foundation of China and the State Key Laboratory of Bio-Organic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences.
关键词 Kinetic resolution total synthesis (+)-1-deoxy-6-epi-castanospermine Kinetic resolution total synthesis (+)-1-deoxy-6-epi-castanospermine
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