location: Current position: Home >> Scientific Research >> Paper Publications

Iodine-mediated cross-dehydrogenative coupling of pyrazolones and alkenes

Hits:

Indexed by:期刊论文

Date of Publication:2018-09-14

Journal:ORGANIC & BIOMOLECULAR CHEMISTRY

Included Journals:SCIE

Volume:16

Issue:34

Page Number:6275-6283

ISSN No.:1477-0520

Abstract:An iodine-mediated alkenylation of pyrazolones with simple alkenes under an air atmosphere has been developed. By this protocol, the pharmaceutically relevant pyrazolone scaffold was directly adorned with a readily transformable olefinic functional group through a cross-dehydrogenative coupling process in moderate to excellent yields. The coupling products could be facilely manipulated by, for example, the Heck reaction and hydrogenation treatment, thus enriching the pyrazolone derivatives. Based on the observation of the reaction intermediate and mechanistical experiments, two possible reaction pathways were proposed.

Pre One:Sulfur-Centered Reactivity of Oxidized Iron-Thiolate Complex toward Unsaturated Hydrocarbon Addition

Next One:Highly beta(Z)-Selective Hydrosilylation of Terminal Alkynes Catalyzed by Thiolate-Bridged Dirhodium Complexes