Answers are grounded in this paper and cite their sources.
Ammonia-borane serves as an efficient substoichiometric (10%) precatalyst for the direct amidation of both aromatic and aliphatic carboxylic acids. In situ generation of amine-boranes precedes the amidation and, unlike the amidation with stoichiometric amine-boranes, this process is facile with 1 equiv of the acid. This methodology has high functional group tolerance and chromatography-free purification but is not amenable for esterification. The latter feature has been exploited to prepare hydroxyl- and thiol-containing amides.
No takes yet. Share an insight, caveat, or question.
Ramachandran et al. (2021) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: