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Thieme Gruppe, Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry, 2, p. 0247-0250, 2004

DOI: 10.1055/s-2003-44968

Wiley-VCH Verlag, ChemInform, 24(35), 2004

DOI: 10.1002/chin.200424112

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A flexible approach for the asymmetric synthesis of N-protected (R)-5-alkyl tetramates and (R)-5-alkyl tetramic acid derivatives

Journal article published in 2004 by Pq-Q. Huang ORCID, 黄培强, Jun Deng
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

A flexible two-step asymmetric approach to N-protected (R)-5-alkyl tetramates and (R)-5-alkyl tetramic acid derivatives is described. The method is based on the diastereoselective alkylation of (R)-phenylglycinol derived tetramates 7 and 8, which are the first synthetic equivalents to chiral nonracemic tetramate 5-carbanionic synthons A.