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Nickel-catalyzed reductive cleavage of aryl alkyl ethers to arenes in absence of external reductant.

ABSTRACT: The reductive cleavage of the C-O bonds of aryl ethers has great potential in organic synthesis. Although several catalysts that can promote the reductive cleavage of aryl ethers have been reported, all such systems require the use of an external reductant, e.g., hydrosilane or hydrogen. Here, we report the development of a new nickel-based catalytic system that can cleave the C-O bonds of ethers in the absence of an external reductant. The hydrogen atom required in this new reductive cleavage reaction is provided by the alkoxy group of the substrate, which serves as an internal reductant. The absence of an external reductant enables the unique chemoselectivity, i.e., the selective reduction of an alkoxy group over alkenes and ketones.

SUBMITTER: Tobisu M

PROVIDER: S-EPMC5659071 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

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Nickel-catalyzed reductive cleavage of aryl alkyl ethers to arenes in absence of external reductant.

Tobisu Mamoru M Morioka Toshifumi T Ohtsuki Akimichi A Chatani Naoto N

Chemical science 20150327 6

The reductive cleavage of the C-O bonds of aryl ethers has great potential in organic synthesis. Although several catalysts that can promote the reductive cleavage of aryl ethers have been reported, all such systems require the use of an external reductant, <i>e.g.</i>, hydrosilane or hydrogen. Here, we report the development of a new nickel-based catalytic system that can cleave the C-O bonds of ethers in the absence of an external reductant. The hydrogen atom required in this new reductive cle ...[more]

PMID: 29511506

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