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dc.contributor.authorPei-Qiang Huang
dc.contributor.author黄培强
dc.contributor.authorZhao-Ying Li
dc.date.accessioned2011-10-16T14:54:21Z
dc.date.available2011-10-16T14:54:21Z
dc.date.issued2005-10
dc.identifier.citationTETRAHEDRON-ASYMMETRY,2005,16(20):3367-3370zh_CN
dc.identifier.issn0957-4166
dc.identifier.urihttp://dx.doi.org/doi:10.1016/j.tetasy.2005.09.009
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/10938
dc.description.abstractStarting from (S)-phenylalanine, an asymmetric synthesis of (S)-homocitric acid lactone was achieved using Seebach's SRS methodology. An intermediate for the synthesis of the (S)-per-homocitric acid lactone has also been synthesized. (c) 2005 Elsevier Ltd. All rights reserved.zh_CN
dc.language.isoenzh_CN
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDzh_CN
dc.titleAsymmetric synthesis of (S)-homocitric acid lactonezh_CN
dc.typeArticlezh_CN


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