Issue 91, 2012

Flow synthesis of arylboronic esters bearing electrophilic functional groups and space integration with Suzuki–Miyaura coupling without intentionally added base

Abstract

We found that an integrated flow microreactor system enables the preparation of boronic esters bearing electrophilic functional groups using organolithium chemistry and that it allows for their use in Suzuki–Miyaura cross-coupling without intentionally added base. Based on this method, cross-coupling of two aryl halides bearing electrophilic functional groups was accomplished to obtain the corresponding biaryl compounds in one flow.

Graphical abstract: Flow synthesis of arylboronic esters bearing electrophilic functional groups and space integration with Suzuki–Miyaura coupling without intentionally added base

Supplementary files

Article information

Article type
Communication
Submitted
26 Aug 2012
Accepted
27 Sep 2012
First published
28 Sep 2012

Chem. Commun., 2012,48, 11211-11213

Flow synthesis of arylboronic esters bearing electrophilic functional groups and space integration with Suzuki–Miyaura coupling without intentionally added base

A. Nagaki, Y. Moriwaki and J. Yoshida, Chem. Commun., 2012, 48, 11211 DOI: 10.1039/C2CC36197C

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