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dc.contributor.authorHuang, PQ
dc.contributor.author黄培强
dc.contributor.authorYe, JL
dc.contributor.authorChen, Z
dc.contributor.authorRuan, YP
dc.contributor.author阮源萍
dc.contributor.authorGao, JX
dc.contributor.author高景星
dc.date.accessioned2012-08-02T01:15:32Z
dc.date.available2012-08-02T01:15:32Z
dc.date.issued2006-08-15
dc.identifier.citationSYNTHETIC COMMUNICATIONS,1998,28(3):417-426zh_CN
dc.identifier.issn0039-7911
dc.identifier.urihttp://dx.doi.org/doi:10.1080/00397919808005095
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/13396
dc.description.abstractA concise and versatile approach to the activated form of(3S, 4R)-statine 6 and its analogues is described. The key steps involve reductive alkylation of (S)-O-tert-butyldimethysilylmalimide 12.zh_CN
dc.language.isoenzh_CN
dc.publisherMARCEL DEKKER INCzh_CN
dc.titleA versatile approach to the activated form of (3S, 4R)-statine and its analogueszh_CN
dc.typeArticlezh_CN


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