Cobalt-catalyzed arylation of aldimines via directed C-H bond functionalization: Addition of 2-arylpyridines and self-coupling of aromatic aldimines

Ke Gao; Naohiko Yoshikai

doi:10.1039/c2cc31114c

Cobalt-catalyzed arylation of aldimines via directed C-H bond functionalization: Addition of 2-arylpyridines and self-coupling of aromatic aldimines

Ke Gao, Naohiko Yoshikai

PHA - Molecular Pharmaceutical Science

Nanyang Technological University

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

108 Citations (Scopus)

Abstract

A cobalt-N-heterocyclic carbene catalyst, in combination with an appropriate Grignard reagent, promotes a chelation-assisted aromatic C-H functionalization reaction via addition to an aromatic aldimine.

Original language	English
Pages (from-to)	4305-4307
Number of pages	3
Journal	Chemical Communications
Volume	48
Issue number	36
DOIs	https://doi.org/10.1039/c2cc31114c
Publication status	Published - 2012 Apr 4

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title = "Cobalt-catalyzed arylation of aldimines via directed C-H bond functionalization: Addition of 2-arylpyridines and self-coupling of aromatic aldimines",

abstract = "A cobalt-N-heterocyclic carbene catalyst, in combination with an appropriate Grignard reagent, promotes a chelation-assisted aromatic C-H functionalization reaction via addition to an aromatic aldimine.",

author = "Ke Gao and Naohiko Yoshikai",

year = "2012",

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doi = "10.1039/c2cc31114c",

language = "English",

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AB - A cobalt-N-heterocyclic carbene catalyst, in combination with an appropriate Grignard reagent, promotes a chelation-assisted aromatic C-H functionalization reaction via addition to an aromatic aldimine.

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Cobalt-catalyzed arylation of aldimines via directed C-H bond functionalization: Addition of 2-arylpyridines and self-coupling of aromatic aldimines

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