SYNTHESIS OF (+)-TETRAHYDROPSEUDODISTOMIN

被引：35

作者：

KNAPP, S

HALE, JJ

机构：

[1] Department of Chemistry, Rutgers The State University of New Jersey, New Brunswick

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1993年 / 58卷 / 10期

关键词：

D O I：

10.1021/jo00062a003

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The stereocontrolled synthesis of (+)-tetrahydropseudodistomin (3) from D-serine features the use of the dibenzyltriazone group for amino protection and establishes the absolute stereochemistry of the naturally occurring calmodulin antagonists pseudodistomin A and B (1 and 2b, respectively).

引用

页码：2650 / 2651

页数：2

共 9 条

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[7] VIAUD MC, 1990, SYNTHESIS-STUTTGART, P130
[8] N-(TRIFLUOROACETYL)AMINO ACIDS .21. REDUCTIVE ELIMINATION OF N-TRIFLUOROACETYL AND N-TRICHLOROACETYL GROUP BY SODIUM BORON HYDRIDE AND APPLICATIONS IN PEPTIDE CHEMISTRY
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