Issue 46, 2018

Synthesis and cycloaddition reactions of strained alkynes derived from 2,2′-dihydroxy-1,1′-biaryls

Abstract

A series of strained alkynes, based on the 2,2′-dihydroxy-1,1′-biaryl structure, were prepared in a short sequence from readily-available starting materials. These compounds can be readily converted into further derivatives including examples containing fluorescent groups with potential for use as labelling reagents. The alkynes are able to react in cycloadditions with a range of azides without the requirement for a copper catalyst, in clean reactions with no observable side reactions.

Graphical abstract: Synthesis and cycloaddition reactions of strained alkynes derived from 2,2′-dihydroxy-1,1′-biaryls

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2018
Accepted
05 Oct 2018
First published
12 Nov 2018
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2018,16, 8965-8975

Synthesis and cycloaddition reactions of strained alkynes derived from 2,2′-dihydroxy-1,1′-biaryls

A. Mistry, R. C. Knighton, S. Forshaw, Z. Dualeh, J. S. Parker and M. Wills, Org. Biomol. Chem., 2018, 16, 8965 DOI: 10.1039/C8OB01768A

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