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Copper-Catalyzed Diboron-Mediated cis-Semi-Hydrogenation of Alkynes under Facile Conditions.


ABSTRACT: Cis-alkenes are ubiquitous in biological molecules, which makes it greatly significant to develop efficient methods toward construction of cis-olefins. Herein, we reported a facile semi-hydrogenation of alkynes to cis-alkenes in an efficient way with cuprous bromide/tributylphosphine as the catalyst and bis(pinacolato)diboron/methanol as the hydrogen donor. The method features convenient and facile reaction conditions, wide substrate scope, high yields, and high stereoselectivity.

SUBMITTER: Zeng Y 

PROVIDER: S-EPMC9656742 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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Copper-Catalyzed Diboron-Mediated <i>cis</i>-Semi-Hydrogenation of Alkynes under Facile Conditions.

Zeng Yuxi Y   Zhang Honggang H   Ma Daofan D   Wang Guangwei G  

Molecules (Basel, Switzerland) 20221025 21


<i>Cis</i>-alkenes are ubiquitous in biological molecules, which makes it greatly significant to develop efficient methods toward construction of <i>cis</i>-olefins. Herein, we reported a facile semi-hydrogenation of alkynes to <i>cis</i>-alkenes in an efficient way with cuprous bromide/tributylphosphine as the catalyst and bis(pinacolato)diboron/methanol as the hydrogen donor. The method features convenient and facile reaction conditions, wide substrate scope, high yields, and high stereoselect  ...[more]

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