91503-62-7Relevant articles and documents
Primary amides. A general nitrogen source for catalytic asymmetric aminohydroxylation of olefins
Demko, Zachary P.,Bartsch, Michael,Sharpless, K. Barry
, p. 2221 - 2223 (2007/10/03)
(equation presented) N-Bromo,N-lithio salts of primary carboxamides have been shown to be efficient nitrogen sources for catalytic asymmetric aminohydroxylation of olefins, behaving much like the parent N-bromoacetamide in these reactions. α-Chloro-N-brom
A CONVENIENT SYNTHESIS OF N-BROMOACETAMIDES BY USE OF SODIUM BROMITE
Kajigaeshi, Shoji,Nakagawa, Takashi,Fujisari, Shizuo
, p. 2045 - 2046 (2007/10/02)
Reaction of aliphatic and aromatic amides in acetic acid with aqueous sodium bromite (NaBrO2) under mild conditions gave N-bromoamides in fairly good yields.