91503-62-7Relevant academic research and scientific papers
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
Organic Synthesis Using Sodium Bromate. II. A Facile Synthesis of N-Bromo Imides and Amides Using Sodium Bromate and Hydrobromic Acid (or Sodium Bromide) in the Presence of Sulfuric Acid
Fujisaki, Shizuo,Hamura, Satoshi,Eguchi, Hisao,Nishida, Akiko
, p. 2426 - 2428 (2007/10/02)
The reaction of imides and amides in water (or aqueous acetic acid) with sodium bromate and hydrobromic acid (or sodium bromide) in the presence of sulfuric acid under mild conditions gave the corresponding N-bromides in high yields.
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.
