Issue 46, 2015

One-pot synthesis of benzoxaborole derivatives from the palladium-catalyzed cross-coupling reaction of alkoxydiboron with unprotected o-bromobenzylalcohols

Abstract

Under very mild conditions, functionalized benzoxaborole derivatives were prepared in good to excellent yields via a palladium-catalyzed Miyaura borylation reaction of readily available unprotected o-bromobenzylalcohols, and bis(pinacolato)diboron (B2pin2) without the assistance of an acid. Blue-light-emitting materials based on spiro benzoxaborole building blocks have been obtained with potential applications in organic electronics and biomedicine.

Graphical abstract: One-pot synthesis of benzoxaborole derivatives from the palladium-catalyzed cross-coupling reaction of alkoxydiboron with unprotected o-bromobenzylalcohols

Supplementary files

Article information

Article type
Paper
Submitted
25 Aug 2015
Accepted
23 Sep 2015
First published
24 Sep 2015

Org. Biomol. Chem., 2015,13, 11362-11368

One-pot synthesis of benzoxaborole derivatives from the palladium-catalyzed cross-coupling reaction of alkoxydiboron with unprotected o-bromobenzylalcohols

J. Zhu, Y. Wei, D. Lin, C. Ou, L. Xie, Y. Zhao and W. Huang, Org. Biomol. Chem., 2015, 13, 11362 DOI: 10.1039/C5OB01781E

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