Synthesis 2017; 49(21): 4775-4782
DOI: 10.1055/s-0036-1590912
special topic
© Georg Thieme Verlag Stuttgart · New York

Developing a Bench-Scale Green Diboration Reaction toward Industrial Application

Albert Farre
a  Department of Chemistry, University of Hull, Cottingham Road, Hull, HU6 7RX, UK
,
Rachel Briggs
a  Department of Chemistry, University of Hull, Cottingham Road, Hull, HU6 7RX, UK
,
Cristina Pubill-Ulldemolins*
b  School of Chemistry, University of St Andrews, St Andrews, KY16 9ST, UK
,
Amadeu Bonet*
a  Department of Chemistry, University of Hull, Cottingham Road, Hull, HU6 7RX, UK
c  Synkotech Biocompatible Materials S.L., Av. Paisos Catalans 18, 43007 Tarragona, Catalonia, Spain   Email: amadeu.bonet@synkotechbio.com
› Author Affiliations
Further Information

Publication History

Received: 12 August 2017

Accepted after revision: 28 August 2017

Publication Date:
10 October 2017 (eFirst)

Dedicated to Prof. Maria Elena Fernandez and Prof. Carles Bo, our scientific parents

Published as part of the Special Topic Modern Strategies for Borylation in Synthesis

Abstract

We report a new methodology for the organocatalytic diboration reaction using inexpensive, sustainable, nontoxic, commercially available halogen salts. This is an educative manuscript for the transformation of laboratory scale reactions into a sustainable approach of appeal to industry.

Supporting Information

 
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