Synthesis 2018; 50(04): 803-808
DOI: 10.1055/s-0036-1591719
paper
© Georg Thieme Verlag Stuttgart · New York

Borane-Catalysed Hydroboration of Alkynes and Alkenes

Nate W. J. Ang
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
Cornelia S. Buettner
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
Scott Docherty
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
Alessandro Bismuto
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
Jonathan R. Carney
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
Jamie H. Docherty
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
Michael J. Cowley
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
,
EaStCHEM School of Chemistry, Joseph Black Building, University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK   Email: Stephen.Thomas@ed.ac.uk
› Author Affiliations
Further Information

Publication History

Received: 04 September 2017

Accepted after revision: 10 October 2017

Publication Date:
20 November 2017 (online)


Published as part of the Bürgenstock Special Section 2017 Future Stars in Organic Chemistry

Abstract

Simple, commercially available borane adducts, H3B·THF and H3B·SMe2, have been used to catalyse the hydroboration of alkynes and alkenes with pinacolborane to give the alkenyl and alkyl boronic esters, respectively. Alkynes and terminal alkenes underwent highly regioselective hydroboration to give the linear boronic ester products. Good functional group tolerance was observed for substrates bearing ester, amine, ether and halide substituents. This catalytic process shows comparable reactivity to transition-metal-catalysed hydroboration protocols.

Supporting Information