Issue 4, 2009
From the journal:

Chemical Communications

A cycloaddition route to novel triazole boronic esters†

Jianhui Huang,a   Simon J. F. Macdonaldb  and  Joseph P. A. Harrity*a  

* Corresponding authors

a Department of Chemistry, University of Sheffield, Sheffield, UK
E-mail: j.harrity@sheffield.ac.uk

b GlaxoSmithKline Research and Development, Gunnels Wood Road, Stevenage, Hertfordshire, UK

Abstract

The [3 + 2] cycloaddition of alkynylboronates and azides provides a direct route to novel triazole boronic esters, the regioselectivity of this process and functionalisation of the heterocycle products is described.

Graphical abstract: A cycloaddition route to novel triazole boronic esters

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Article information

DOI
https://doi.org/10.1039/B817052E
Article type
Communication
Submitted
29 Sep 2008
Accepted
20 Oct 2008
First published
14 Nov 2008

Chem. Commun., 2009, 436-438

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A cycloaddition route to novel triazole boronic esters

J. Huang, S. J. F. Macdonald and J. P. A. Harrity, Chem. Commun., 2009, 436 DOI: 10.1039/B817052E

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