4.7 Article

Room Temperature Cross-Coupling of Highly Functionalized Organozinc Reagents with Thiomethylated N-Heterocycles by Nickel Catalysis

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 75, Issue 6, Pages 2131-2133

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo1001615

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Funding

  1. DFG and the European Research Council (ERC)

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A variety of thiomethyl-substituted N-heterocycles such as pyridines, isoquinolines, pyrimidines, pyrazines, pyridazines, quinazolines, triazines, benzothiazoles, or benzoxazoles undergo smooth Ni-catalyzed cross-coupling reactions with functionalized aryl-, heteroaryl-, alkyl-, and benzylic zinc reagents using an Inexpensive Ni(acac)(2)/DPE-Phos catalytic system at 25 degrees C.

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