Literature DB >> 33530687

Preparation of α-Perfluoroalkyl Ketones from α,β-Unsaturated Ketones via Formal Hydroperfluoroalkylation.

Kalipada Jana1, Isao Mizota1, Armido Studer1.   

Abstract

Formal hydroperfluoroalkylation of enones is achieved in a two-step process comprising conjugate hydroboration and subsequent radical perfluoroalkylation. The 1,4-hydroboration of the enone is conducted in the absence of any transition metal catalyst with catecholborane in 1,2-dichloroethane, and the generated boron enolate is in situ α-perfluoroalkylated with a perfluoroalkyl iodide upon blue LED irradiation in the presence of an amine additive. Both reactions proceed under very mild conditions at room temperature.

Entities:  

Year:  2021        PMID: 33530687     DOI: 10.1021/acs.orglett.0c04260

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Crystal structure and Hirshfeld surface analysis of 7,7-dimethyl-2-phenyl-3,3a,4,6,7,8,9,9a-octa-hydro-1H-benzo[f]iso-indole-1,5(2H)-dione.

Authors:  Dong Cheng; Xinlei Gao; Jiating Huang; Xiang-Zhen Meng
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2022-03-10

2.  Allylboronic Esters as Acceptors in Radical Addition, Boron 1,2-Migration, and Trapping Cascades.

Authors:  Kalipada Jana; Armido Studer
Journal:  Org Lett       Date:  2022-01-26       Impact factor: 6.005

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.