SYNTHESIS OF CYCLIC ACYLATED ENAMINO ESTER DIPEPTIDE ANALOGS VIA THE BROMOLACTONIZATION OF A KETO ACID PHOSPHORANE

被引：29

作者：

ABELL, AD

TAYLOR, JM

机构：

[1] Department of Chemistry, University of Canterbury, Christchurch

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1993年 / 58卷 / 01期

关键词：

D O I：

10.1021/jo00053a006

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The acylated cyclic enamino ester dipeptide analogues 12, 13, and 17-19 have been prepared via lactonization of the keto acid phosphorane 8 followed by incorporation of an amino acid into the product enol lactones 9, 10, and 16.

引用

页码：14 / 15

页数：2

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