| Literature DB >> 26420729 |
Hui Wang1, Julian Koeller1, Weiping Liu1, Lutz Ackermann2.
Abstract
C-H/N-O functionalizations by cobalt(III) catalysis allowed the expedient synthesis of a broad range of isoquinolines. Thus, internal and challenging terminal alkynes proved to be viable substrates for an isohypsic annulation, which was shown to proceed by a facile C-H cobaltation.Entities:
Keywords: CH activation; N-O cleavage; alkyne; cobalt; isoquinoline
Year: 2015 PMID: 26420729 DOI: 10.1002/chem.201503624
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236