

Publisher: John Wiley & Sons Inc
E-ISSN: 1099-0739|29|8|524-527
ISSN: 0268-2605
Source: APPLIED ORGANOMETALLIC CHEMISTRY (ELECTRONIC), Vol.29, Iss.8, 2015-08, pp. : 524-527
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
An efficient Pd‐catalyzed desulfitative approach to C‐3 arylation of indolizine derivatives has been developed, and the protocol uses readily available arylsulfonyl chlorides as the arylation reagent under nitrogen. This transformation was performed in a mixed solvent of 1‐methyl‐2‐pyrrolidone and dimethoxyethane using simple triphenylphosphine as a ligand, which provides a new method for the C‐3 arylation of indolizines. Copyright © 2015 John Wiley & Sons, Ltd.
Related content


Palladium‐Catalyzed Direct C–H Arylation of Dicyanobenzenes
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Vol. 2015, Iss. 15, 2015-05 ,pp. :




Desulfitative C‐Arylation of Glycals by Using Benzenesulfonyl Chlorides
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Vol. 2015, Iss. 3, 2015-01 ,pp. :


Palladium‐Catalyzed Direct CH Arylation of Isoxazoles at the 5‐Position
ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 33, 2015-08 ,pp. :


Palladium‐Catalyzed Direct CH Arylation of Isoxazoles at the 5‐Position
ANGEWANDTE CHEMIE, Vol. 127, Iss. 33, 2015-08 ,pp. :