| Literature DB >> 30565825 |
Xuan Jiang1, Mao-Mao Zhang1, Wei Xiong1, Liang-Qiu Lu1, Wen-Jing Xiao1,2.
Abstract
The palladium-catalyzed Heck reaction is a well-known, Nobel Prize winning transformation for producing alkenes. Unlike the alkenyl and aryl variants of the Heck reaction, the alkyl-Heck reaction is still underdeveloped owing to the competitive side reactions of alkyl-palladium species. Herein, we describe the development of a deaminative alkyl-Heck-type reaction that proceeds through C-N bond activation by visible-light photoredox catalysis. A variety of aliphatic primary amines were found to be efficient starting materials for this new process, affording the corresponding alkene products in good yields under mild reaction conditions. Moreover, this strategy was successfully applied to deaminative carbonylative alkyl-Heck-type reactions.Entities:
Keywords: Heck reaction; amines; carbonylative reactions; deaminative transformations; photocatalysis
Year: 2019 PMID: 30565825 DOI: 10.1002/anie.201813689
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336