| Literature DB >> 27690249 |
Gongming Zhu1,2, Guangjun Bao2, Yiping Li2, Junxian Yang2, Wangsheng Sun2, Jing Li1,2, Liang Hong1, Rui Wang1,2.
Abstract
A highly enantioselective oxidative dearomatization of naphthols with quinones catalyzed by a chiral spirocyclic phosphoric acid is described. The strategy provides concise access to enantioenriched cyclohexadienones with a quinone moiety. Remarkably, the obtained products could be easily transformed to a potentially useful dihydronaphtho[2,1-b]benzofuran scaffold.Entities:
Year: 2016 PMID： 27690249 DOI： 10.1021/acs.orglett.6b02609
Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005