NEW APPROACHES TO THE SYNTHESIS OF TRANS-ALKENE ISOSTERES OF DIPEPTIDES

被引：82

作者：

SPALTENSTEIN, A ^{[1
]}

CARPINO, PA ^{[1
]}

MIYAKE, F ^{[1
]}

HOPKINS, PB ^{[1
]}

机构：

[1] UNIV WASHINGTON,DEPT CHEM,DANIEL BAGLEY LABS,SEATTLE,WA 98195

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1987年 / 52卷 / 17期

关键词：

D O I：

10.1021/jo00226a007

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3759 / 3766

页数：8

共 27 条

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[6] A METHOD FOR THE DETERMINATION OF THE CONFIGURATION OF THE L-PRO-L, D-PHE PSEUDODIPEPTIDE ISOMERS CONTAINING A TRANS-ETHYLENE ISOSTERIC REPLACEMENT OF THE PEPTIDE-BOND
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[7] ALLYLSELENIDES POSSESSING A TERMINAL DOUBLE-BOND 1ST REGIOSELECTIVE SYNTHESIS AND REACTIONS
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[J]. TETRAHEDRON LETTERS, 1983, 24 (32) : 3413 - 3416
[8] EVANS DA, 1982, J AM CHEM SOC, V104, P1727
[9] FEARON K, IN PRESS J MED CHEM
[10] HANESSIAN S, 1979, Tetrahedron Letters, P3391

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