Palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine

Chunhui Huang; Alexandros Giokaris; Vladimir Gevorgyan

doi:10.1246/cl.2011.1053

Palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine

Chunhui Huang, Alexandros Giokaris, Vladimir Gevorgyan

Research output: Contribution to journal › Article › peer-review

22 Scopus citations

Abstract

A direct palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine with aryl bromides has been developed. This reaction is quite general with respect to the aryl or hetaryl bromide.

Original language	English (US)
Pages (from-to)	1053-1054
Number of pages	2
Journal	Chemistry Letters
Volume	40
Issue number	9
DOIs	https://doi.org/10.1246/cl.2011.1053
State	Published - 2011
Externally published	Yes

ASJC Scopus subject areas

General Chemistry

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title = "Palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine",

abstract = "A direct palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine with aryl bromides has been developed. This reaction is quite general with respect to the aryl or hetaryl bromide.",

author = "Chunhui Huang and Alexandros Giokaris and Vladimir Gevorgyan",

year = "2011",

doi = "10.1246/cl.2011.1053",

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AU - Huang, Chunhui

AU - Giokaris, Alexandros

AU - Gevorgyan, Vladimir

PY - 2011

Y1 - 2011

N2 - A direct palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine with aryl bromides has been developed. This reaction is quite general with respect to the aryl or hetaryl bromide.

AB - A direct palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine with aryl bromides has been developed. This reaction is quite general with respect to the aryl or hetaryl bromide.

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AN - SCOPUS:80052605209

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JO - Chemistry Letters

JF - Chemistry Letters

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Palladium-catalyzed highly regioselective C-3 arylation of imidazo[1,5-a]pyridine

Abstract

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