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Literature DB >> 19924879

Highly regioselective palladium-catalyzed oxidative coupling of indolizines and vinylarenes via C-H bond cleavage.

Abstract

A highly regioselective oxidative coupling reaction between indolizines and vinylarenes has been accomplished in the presence of palladium catalysts to give only the branched alpha-product in high efficiency. The regioselectivity is promoted significantly by bidentate nitrogen ligands.

Entities: Chemical

Year: 2009 PMID： 19924879 DOI： 10.1021/ol902315w

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

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Cited

2 in total

1. Regioselective formation of alpha-vinylpyrroles from the ruthenium-catalyzed coupling reaction of pyrroles and terminal alkynes involving C-H bond activation.

Authors: Ruili Gao; Chae S Yi
Journal: J Org Chem Date: 2010-05-07 Impact factor: 4.354

2. Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C-H Functionalization.

Authors: Phillippa Cooper; Giacomo E M Crisenza; Lyman J Feron; John F Bower
Journal: Angew Chem Int Ed Engl Date: 2018-09-26 Impact factor: 15.336

2 in total