Issue 67, 2017

One-pot borylation/Suzuki–Miyaura sp2–sp3 cross-coupling

Abstract

We describe the first one-pot borylation/Suzuki–Miyaura sp2–sp3 cross-coupling between readily available aryl (pseudo)halides and activated alkyl chlorides. This method streamlines the synthesis of diaryl methanes, α-aryl carbonyls and allyl aryl compounds, substructures that are commonly found in life changing drug molecules.

Graphical abstract: One-pot borylation/Suzuki–Miyaura sp2–sp3 cross-coupling

Supplementary files

Article information

Article type
Communication
Submitted
29 Jun 2017
Accepted
01 Aug 2017
First published
02 Aug 2017

Chem. Commun., 2017,53, 9364-9367

One-pot borylation/Suzuki–Miyaura sp2–sp3 cross-coupling

L. Whitaker, H. Y. Harb and A. P. Pulis, Chem. Commun., 2017, 53, 9364 DOI: 10.1039/C7CC05037B

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