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Issue 20, 2015
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Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether

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Abstract

Reactions of boranes with Te(CCPh)2 proceed via initial intermolecular 1,1-carboboration followed by either an intramolecular carboboration or an FLP addition to a second molecule of the intermediate, yielding 1-bora-4-tellurocyclohexa-2,5-diene heterocycles or tricylic derivatives of 1,4-ditellurocyclohexa-2,5-diene, respectively. The latter species is also shown to convert to the former upon heating.

Graphical abstract: Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether

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Supplementary files

Article information


Submitted
19 Nov 2014
Accepted
04 Feb 2015
First published
04 Feb 2015

Chem. Commun., 2015,51, 4287-4289
Article type
Communication
Author version available

Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether

F. A. Tsao, Alan. J. Lough and D. W. Stephan, Chem. Commun., 2015, 51, 4287
DOI: 10.1039/C4CC09258A

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