| Literature DB >> 32602725 |
Zhaohui Li1, Long Liu1, Kaiqiang Xu1, Tianzeng Huang1, Xinyi Li1, Bin Song1, Tieqiao Chen1.
Abstract
A palladium-catalyzed N-acylation of tertiary amines by carboxylic acids was achieved through C-N cleavage. This reaction showed a wide substrate scope. Both aromatic and aliphatic acids served well as the acylating reagents and coupled with tertiary amines to produce the corresponding amides in good to excellent yields. With the strategy, bioactive carboxylic acids were also efficiently modified, highlighting the synthetic value of the process in organic synthesis.Entities:
Year: 2020 PMID: 32602725 DOI: 10.1021/acs.orglett.0c01869
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005