Publication:
Stereoselective synthesis of β-carboethoxy-γ-lactams via imino Mukaiyama aldol-type reaction of 1,4-bis(trimethylsilyloxy)-1,4-diethoxy-1,3-butadiene

Issued Date

2007-05-14

Resource Type

Article

ISSN

00404020

DOI

10.1016/j.tet.2007.03.006

Other identifier(s)

2-s2.0-34047262894

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron. Vol.63, No.20 (2007), 4328-4337

Suggested Citation

Manat Pohmakotr, Nattawut Yotapan, Patoomratana Tuchinda, Chutima Kuhakarn, Vichai Reutrakul Stereoselective synthesis of β-carboethoxy-γ-lactams via imino Mukaiyama aldol-type reaction of 1,4-bis(trimethylsilyloxy)-1,4-diethoxy-1,3-butadiene. Tetrahedron. Vol.63, No.20 (2007), 4328-4337. doi:10.1016/j.tet.2007.03.006 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/24197

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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

Author(s)

Manat Pohmakotr
 Nattawut Yotapan
 Patoomratana Tuchinda
 Chutima Kuhakarn
 Vichai Reutrakul

Other Contributor(s)

Mahidol University

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.

Keyword(s)

Biochemistry, Genetics and Molecular Biology
 Chemistry
 Pharmacology, Toxicology and Pharmaceutics

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URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/24197

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Scopus 2006-2010