| Literature DB >> 28225623 |
Qiao Yan1, Emma Gin1, Malgorzata Wasinska-Kalwa1, Martin G Banwell1, Paul D Carr1.
Abstract
The title natural products 2-7 have been prepared by reductive cyclization of the relevant 2-arylcyclohex-2-en-1-one (e.g. 20) to the corresponding tetrahydrocarbazole and dehydrogenation (aromatization) of this to give the target carbazole (e.g. 4). Compounds such as 20 were prepared using a palladium-catalyzed Ullmann cross-coupling reaction between the appropriate 2-iodocyclohex-2-en-1-one and o-halonitrobenzene.Entities:
Year: 2017 PMID: 28225623 DOI: 10.1021/acs.joc.7b00044
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354