BETA-STANNYLATED YNAMINES AS AMINOETHYNYLATION REAGENTS

被引：42

作者：

HIMBERT, G

机构：

[1] Fachbereich Chemie der Universität, Kaiserslautern, D-6750

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1979年 / 18卷 / 05期

关键词：

D O I：

10.1002/anie.197904051

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Introduction of a R2NCC group, e.g. into acyl chlorides and imidoyl chlorides, is possible with the reagent 1. The reactive CC linked C2 unit in the product permits further reactions. (Figure Presented.) Copyright © 1979 by Verlag Chemie, GmbH, Germany

引用

页码：405 / 406

页数：2

共 10 条

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[2] INVESTIGATIONS ON DIAZO-COMPOUNDS AND AZIDES .25. AZIDE ADDITIONS ON (SILYLETHYNYL)AMINES, (GERMYLETHYNYL)AMINES, AND (STANNYLETHYNYL)AMINES [J].

HIMBERT, G ;

FRANK, D ;

REGITZ, M .

CHEMISCHE BERICHTE-RECUEIL, 1976, 109 (01) :370-394

[3]

HIMBERT G, 1972, SYNTH-INT J METHODS, P571

[4]

HIMBERT G, 1979, J CHEM RES-S, P88

[5]

HIMBERT G, 1978, J CHEM RES, P102

[6]

HIMBERT G, UNPUBLISHED

[7]

HIMBERT G, 1978, J CHEM RES M, P1445

[8] REACTIONS OF YNAMINES [J].

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[9] PUSH-PULL ACETYLENES AS REAGENTS FOR PEPTIDE-SYNTHESIS [J].

LIENHARD, U ;

FAHRNI, HP ;

NEUENSCHWANDER, M .

HELVETICA CHIMICA ACTA, 1978, 61 (05) :1609-1621

[10]

REGITZ M, UNPUBLISHED

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