Issue 47, 2017

Facile access to unsymmetrically substituted tellurium–boron based heterocycles

Abstract

Reactions of Te–B heterocycles Te((Ph)C[double bond, length as m-dash]C(C6F5))2B(C6F5) 1 with alcohols is shown to afford species of the form Te((Ph)C[double bond, length as m-dash]C(C6F5))2BOR. The subsequent reaction with either 4-Br-C6H4CCH or 3-(C4H3S)CCH proceeds with the liberation of C6F5CCPh to give unsymmetrically substituted Te–B based heterocycles of the form Te((Ph)C[double bond, length as m-dash]C(C6F5))(HC[double bond, length as m-dash]CR)BOCH2Ph.

Graphical abstract: Facile access to unsymmetrically substituted tellurium–boron based heterocycles

Supplementary files

Article information

Article type
Communication
Submitted
10 May 2017
Accepted
19 May 2017
First published
19 May 2017

Chem. Commun., 2017,53, 6311-6314

Facile access to unsymmetrically substituted tellurium–boron based heterocycles

F. A. Tsao and D. W. Stephan, Chem. Commun., 2017, 53, 6311 DOI: 10.1039/C7CC03648E

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