| Literature DB >> 31971810 |
Qing Huang1, Ya-Wei Li1, Xiao-Shan Ning2, Guo-Qing Jiang1, Xiao-Wei Zhang1, Jian-Ping Qu1, Yan-Biao Kang2.
Abstract
A regioselective Wacker-Tsuji oxidation of internal olefins in tBuOH has been developed using oxygen as the terminal oxidant and tert-butyl nitrite as the simple organic redox cocatalyst without the involvement of hazardous cocatalysts or harsh reaction conditions. A series of internal olefins bearing various functional groups can be oxidized to the corresponding substituted ketones in generally good yields with high regioselectivities.Entities:
Year: 2020 PMID: 31971810 DOI: 10.1021/acs.orglett.9b04503
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005