Journal
TETRAHEDRON
Volume 71, Issue 47, Pages 8871-8875Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2015.10.011
Keywords
Borylation; Suzuki-Miyaura; Cross-coupling; One-pot; Arenes
Categories
Funding
- National Science Foundation of China [21172035, 21302018]
- Research Fund for the Doctoral Program of Higher Education of China [20120075120017, 20120075110001]
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One-step synthesis of several alpha,omega pinacol boronates starting from m-dibromobenzene derivative and bis(pinacolato)diboron through Miyaura reaction has been reported. The present approach provided low to moderate yields of monomer boronates, and trace to low yields of dimmer, trimer and tetramer boronates. Furthermore, the resulted boronates can be followed by Suzuki-Miyaura cross-coupling without purification, which enhances the practical usefulness of this method. (C) 2015 Elsevier Ltd. All rights reserved.
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