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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/24197
Title: Stereoselective synthesis of β-carboethoxy-γ-lactams via imino Mukaiyama aldol-type reaction of 1,4-bis(trimethylsilyloxy)-1,4-diethoxy-1,3-butadiene
Authors: Manat Pohmakotr
Nattawut Yotapan
Patoomratana Tuchinda
Chutima Kuhakarn
Vichai Reutrakul
Mahidol University
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 14-May-2007
Citation: Tetrahedron. Vol.63, No.20 (2007), 4328-4337
Abstract: The reaction of the (bis)trimethylsilyloxy derivative of diethyl succinate with imines in the presence of ZnCl2provides a general stereoselective entry to β-carboethoxy-γ-lactams. © 2007 Elsevier Ltd. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34047262894&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/24197
ISSN: 00404020
Appears in Collections:Scopus 2006-2010

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