| Literature DB >> 29767992 |
Wei Xu1, Gaonan Wang1, Xin Xie1, Yuanhong Liu1.
Abstract
A gold-catalyzed cycloisomerization of ynamide-ynes via a formal dehydro-Diels-Alder reaction has been developed, providing an attractive route to diversely substituted benzo[ b]carbazoles. The reaction likely proceeds via regioselective attack of the pendant alkyne moiety to a keteniminium ion intermediate followed by benzannulation. The method offers several advantages such as high efficiency, mild reaction conditions, and wide functional group tolerance and serves as a highly useful complement to the thermal DDA reactions of ynamide-ynes.Entities:
Year: 2018 PMID: 29767992 DOI: 10.1021/acs.orglett.8b01145
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005