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Cu(II)-Catalyzed Homocouplings of (Hetero)Arylboronic Acids with the Assistance of 2-O-Methyl-d-Glucopyranose.


ABSTRACT: This is the first report of a natural ligand improving the copper-catalyzed homocouplings of (hetero)arylboronic acids. Various important synthetic biaryl intermediates in organic synthesis could be assembled via this method. To gain insight into this reaction, in situ React IR technology was used to confirm the effectivity of this catalyst system. This protocol could provide important biaryl compounds in high yields within a short time.

SUBMITTER: Yuan C 

PROVIDER: S-EPMC6832226 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Cu(II)-Catalyzed Homocouplings of (Hetero)Arylboronic Acids with the Assistance of 2-<i>O</i>-Methyl-d-Glucopyranose.

Yuan Chunling C   Zheng Li L   Zhao Yingdai Y  

Molecules (Basel, Switzerland) 20191012 20


This is the first report of a natural ligand improving the copper-catalyzed homocouplings of (hetero)arylboronic acids. Various important synthetic biaryl intermediates in organic synthesis could be assembled via this method. To gain insight into this reaction, in situ React IR technology was used to confirm the effectivity of this catalyst system. This protocol could provide important biaryl compounds in high yields within a short time. ...[more]

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