Literature DB >> 31971810

Regioselective Wacker-Type Oxidation of Internal Olefins in tBuOH Using Oxygen as the Sole Oxidant and tBuONO as the Organic Redox Cocatalyst.

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


  2 in total

1.  Carbonyl 1,2-transposition through triflate-mediated α-amination.

Authors:  Zhao Wu; Xiaolong Xu; Jianchun Wang; Guangbin Dong
Journal:  Science       Date:  2021-11-04       Impact factor: 63.714

2.  Iron-Catalyzed Wacker-type Oxidation of Olefins at Room Temperature with 1,3-Diketones or Neocuproine as Ligands*.

Authors:  Florian Puls; Philipp Linke; Olga Kataeva; Hans-Joachim Knölker
Journal:  Angew Chem Int Ed Engl       Date:  2021-05-14       Impact factor: 15.336

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.