| Literature DB >> 28485600 |
Saima Perveen1, Zhifei Zhao1, Guoxiang Zhang1, Jian Liu1, Muhammad Anwar1, Xinqiang Fang1.
Abstract
1,2-Dihydronaphthalenes are important molecules in both medicinal and synthetic chemistry, but methods for the catalytic asymmetric construction of this class of molecules are limited. The diastereo- and enantioselective N-heterocyclic carbene-catalyzed cascade annulation reactions using benzodiketones and enals under oxidative conditions, which afford a variety of 1,2-dihydronaphthalenes with two adjacent stereocenters in up to 99% yield, with >20:1 dr, and up to 99% ee, are reported. Furthermore, the product can be easily transformed to a series of useful compounds such as alcohol, amide, and epoxide.Entities:
Year: 2017 PMID: 28485600 DOI: 10.1021/acs.orglett.7b00555
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005