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dc.contributor.authorJing-Xing Du
dc.contributor.authorHui-Ying Huang
dc.contributor.authorPei-Qiang Huang
dc.contributor.author黄培强
dc.date.accessioned2011-12-13T01:22:49Z
dc.date.available2011-12-13T01:22:49Z
dc.date.issued2004-10
dc.identifier.citationTETRAHEDRON-ASYMMETRY,2004,15(21):3461-3466zh_CN
dc.identifier.issn0957-4166
dc.identifier.urihttp://dx.doi.org/doi:10.1016/j.tetasy.2004.09.020
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/11369
dc.description.abstractBased on the highly regio- and diastereoselective reductive-ethoxycarbonylmethylation of protected (S)-malimide 4, a new approach to the Geissman-Waiss lactone 1 and a key intermediate 3 for the synthesis of pyrrolidine trans-lactones (e.g., 2) is described. The synthesis features a one-step and a two-step chemoselective reduction of an amide carbonyl in the presence of an ester group as the key steps. (C) 2004 Elsevier Ltd. All rights reserved.zh_CN
dc.language.isoenzh_CN
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDzh_CN
dc.titleA novel approach to the Geissman-Waiss lactone and a key intermediate in the synthesis of pyrrolidine trans-lactoneszh_CN
dc.typeArticlezh_CN


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