A NOVEL SYNTHESIS OF K-13

被引：46

作者：

BEUGELMANS, R ^{[1
]}

BIGOT, A ^{[1
]}

ZHU, JP ^{[1
]}

机构：

[1] CNRS,INST CHIM SUBST NAT,F-91198 GIF SUR YVETTE,FRANCE

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 40期

关键词：

D O I：

10.1016/0040-4039(94)85322-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new and concise synthesis of 17-membered macrocyclic tripeptide K-13 is achieved featuring intramolecular SNAr reaction as a key step.

引用

收藏

页码：7391 / 7394

页数：4

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共 35 条

[31] ASYMMETRIC SYNTHESES VIA HETEROCYCLIC INTERMEDIATES .6. ENANTIOSELECTIVE SYNTHESIS OF (R)-AMINO ACIDS USING L-VALINE AS CHIRAL AGENT [J].

SCHOLLKOPF, U ;

GROTH, U ;

DENG, C .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1981, 20 (09) :798-799

[32] PIPERAZINOMYCIN, A NEW ANTIFUNGAL ANTIBIOTIC .1. FERMENTATION, ISOLATION, CHARACTERIZATION AND BIOLOGICAL PROPERTIES [J].

TAMAI, S ;

KANEDA, M ;

NAKAMURA, S .

JOURNAL OF ANTIBIOTICS, 1982, 35 (09) :1130-1136

[33] STRUCTURAL STUDIES ON SOME ANTIBIOTICS OF THE VANCOMYCIN GROUP, AND ON THE ANTIBIOTIC-RECEPTOR COMPLEXES, BY H-1-NMR [J].

WILLIAMS, DH .

ACCOUNTS OF CHEMICAL RESEARCH, 1984, 17 (10) :364-369

[34] D-ALANYL-D-ALANINE LIGASES AND THE MOLECULAR MECHANISM OF VANCOMYCIN RESISTANCE [J].

WRIGHT, GD ;

WALSH, CT .

ACCOUNTS OF CHEMICAL RESEARCH, 1992, 25 (10) :468-473

[35] K-13, A NOVEL INHIBITOR OF ANGIOTENSIN-I CONVERTING ENZYME PRODUCED BY MICROMONOSPORA-HALOPHYTICA SUBSP EXILISIA .2. STRUCTURE DETERMINATION [J].

YASUZAWA, T ;

SHIRAHATA, K ;

SANO, H .

JOURNAL OF ANTIBIOTICS, 1987, 40 (04) :455-458

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