| Literature DB >> 26449515 |
Xiangjin Lian1, Lili Lin1, Guojin Wang1, Xiaohua Liu1, Xiaoming Feng2.
Abstract
A catalytic asymmetric dearomatization of 2-naphthols with azodicarboxylates has been accomplished by using a N,N'-dioxide-scandium(III) complex as a chiral catalyst. A number of optically active β-naphthalenone compounds with a nitrogen-containing quaternary carbon stereocenter were obtained in up to 99 % yield and up to 99 % ee under mild reaction conditions. The reaction could be scaled up to a gram-scale with the yield and ee maintained. Based on these experiments and on previous reports, a possible transition state was proposed.Entities:
Keywords: amination reaction; asymmetric catalysis; dearomatization; naphthols; scandium
Year: 2015 PMID: 26449515 DOI: 10.1002/chem.201503276
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236