Issue 22, 2014

Silyl alkynylphosphine-boranes: key precursors of triazolylphosphines via tandem desilylation-Click chemistry

Abstract

A versatile synthesis of 1,2,3-triazolyl-4-phosphines from the borane complexes of phosphino-alkynes is reported. The efficiency of the procedure relies on the use of readily available silyl-protected alkynylphosphine-boranes, which were subjected to desilylation with TBAF followed by copper-catalyzed azide–alkyne-cycloaddition in one pot. Subsequent treatment with DABCO afforded the targeted triazolylphosphines in high yields. The reported method was applied to the synthesis of the first example of an enantioenriched P-stereogenic triazolylphosphine (98.8% ee).

Graphical abstract: Silyl alkynylphosphine-boranes: key precursors of triazolylphosphines via tandem desilylation-Click chemistry

Supplementary files

Article information

Article type
Paper
Submitted
20 Feb 2014
Accepted
25 Mar 2014
First published
27 Mar 2014

Org. Biomol. Chem., 2014,12, 3635-3640

Silyl alkynylphosphine-boranes: key precursors of triazolylphosphines via tandem desilylation-Click chemistry

R. Veillard, E. Bernoud, I. Abdellah, J. Lohier, C. Alayrac and A. Gaumont, Org. Biomol. Chem., 2014, 12, 3635 DOI: 10.1039/C4OB00397G

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