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α‐Aminoaldehydes from Enamines and Chloramine‐T
Author(s) -
Dyong Ingolf,
LamChi Quan
Publication year - 1979
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.197909331
Subject(s) - chloramine , aldehyde , chloramine t , chemistry , organic chemistry , chlorine , catalysis
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.