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Asymmetric total synthesis of (+)-1-deoxy-6-epi-castanospermine
引用本文:徐一鸣,周维善. Asymmetric total synthesis of (+)-1-deoxy-6-epi-castanospermine[J]. 中国化学, 1998, 16(1): 34-44. DOI: 10.1002/cjoc.19980160107
作者姓名:徐一鸣  周维善
作者单位:Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
基金项目: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.
摘    要:(+)-1-Deoxy-6-epi-castanospermine was asymmetrically synthesized in ten steps from α-furfuryl amine derivative 6 in 2.9% overall yield. The kinetic resolution of α-furfuryl amine derivative 6 and Sharpless AD reaction of 14 were used as key steps.


Asymmetric total synthesis of (+)-1-deoxy-6-epi-castanospermine
XU,Yi-Ming ZHOU,Wei-Shan. Asymmetric total synthesis of (+)-1-deoxy-6-epi-castanospermine[J]. Chinese Journal of Chemistry, 1998, 16(1): 34-44. DOI: 10.1002/cjoc.19980160107
Authors:XU  Yi-Ming ZHOU  Wei-Shan
Affiliation:XU,Yi-Ming ZHOU,Wei-ShanShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
Abstract:(+)-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.
Keywords:Kinetic resolution   total synthesis   (+)-1-deoxy-6-epi-castanosperrnine
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