ALPHA-AMINOALDEHYDES FROM ENAMINES AND CHLORAMINE-T

被引：8

作者：

DYONG, I

QUAN, LC

机构：

[1] Organisch-Chemisches Institut, Universität, Münster, D-4400

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1979年 / 18卷 / 12期

关键词：

D O I：

10.1002/anie.197909331

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A facile entry to the α‐amino aldehyde group, which occurs in antibiotic sugars and other natural products, is provided by the reaction of enamines 1 with chloramine T. The conditions are very mild and the yields are high. (Figure Presented.) Copyright © 1979 by Verlag Chemie, GmbH, Germany

引用

页码：933 / 933

页数：1

共 14 条

[1]

CHONG AO, 1977, J AM CHEM SOC, V99, P3402

[2]

DUHAMEL L, 1972, TETRAHEDRON LETT, P4743

[3]

DUHAMEL L, 1975, B SOC CHIM FR II-CH, P329

[4] SYNTHESES OF BIOLOGICALLY IMPORTANT CARBOHYDRATES .19. REGIOSELECTIVITY OF THE VIC CIS-OXYAMINATION OF 3,4-UNSATURATED CARBOHYDRATES - DIRECTED SYNTHESES OF 4-AMINO-4-DEOXYALDOSIDES AND OF 3-AMINO-3-DEOXYALDOSIDES [J].