| Literature DB >> 28829610 |
Guangrong Meng1, Roger Lalancette1, Roman Szostak2, Michal Szostak1.
Abstract
Despite recent progress in catalytic cross-coupling technologies, the direct activation of N-alkyl-N-aryl amides has been a challenging transformation. Here, we report the first Suzuki cross-coupling of N-methylamino pyrimidyl amides (MAPA) enabled by the controlled nN → πAr conjugation and the resulting remodeling of the partial double bond character of the amide bond. The new mode of amide activation is suitable for generating acyl-metal intermediates from unactivated primary and secondary amides.Entities:
Year: 2017 PMID: 28829610 DOI: 10.1021/acs.orglett.7b02288
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005