| Literature DB >> 31021096 |
Suhas Shahaji Gawali1, Biplab Keshari Pandia1, Chidambaram Gunanathan1.
Abstract
A simple protocol of manganese catalyzed selective α-alkenylation of ketones using primary alcohols is reported. The reactions proceeded well with a low loading of catalyst (0.3 mol %). The overall transformation operates through O-H bond activation of primary alcohols via dearomatization-aromatization metal ligand cooperation in the catalyst to provide the corresponding aldehydes, which further undergo condensation with methylene ketones to deliver α,β-unsaturated ketones. This selective α-alkenylation proceeds with the release of water and liberation of molecular hydrogen.Entities:
Year: 2019 PMID: 31021096 DOI: 10.1021/acs.orglett.9b01327
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005