Publication:
Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction

Issued Date

2020-06-01

Resource Type

Article

ISSN

00201693

DOI

10.1016/j.ica.2020.119538

Other identifier(s)

2-s2.0-85080088425

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Inorganica Chimica Acta. Vol.506, (2020)

Suggested Citation

Phongsakorn Boontiem, Supavadee Kiatisevi Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction. Inorganica Chimica Acta. Vol.506, (2020). doi:10.1016/j.ica.2020.119538 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/53637

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Title

Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction

Author(s)

Phongsakorn Boontiem
 Supavadee Kiatisevi

Other Contributor(s)

Mahidol University

Abstract

© 2020 Elsevier B.V. Facile and economical method for Miyaura borylation reaction between B2pin2 and aryl bromides is reported. The catalytic system containing 2 mol% PdCl2(PPh3)2 and KOAc serves to enable borylations to occur under solvent-free and atmospheric conditions. The developed protocol can be applied to synthesize symmetrical and unsymmetrical biaryls via one-pot two-step Suzuki–Miyaura cross-coupling reaction and also offers the up-scalability.

Keyword(s)

Chemistry
 Materials Science

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/53637

Collections

Scopus 2020