ChemInform Abstract: Highly Selective Catalytic trans‐Hydroboration of Alkynes Mediated by Borenium Cations and B(C6F5)3

Utilization of highly Lewis‐acidic boranes allows for transition metal‐free hydroboration of (hetero)aryl‐ and vinyl substituted terminal alkynes.

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Veröffentlicht in:	ChemInform 2016-08, Vol.47 (36), p.no-no
Hauptverfasser:	McGough, John S., Butler, Samuel M., Cade, Ian A., Ingleson, Michael J.
Format:	Artikel
Sprache:	eng
Schlagworte:	alkenes (benzene compounds) e/z‐selectivity (incl. e/z‐isomerism) hydroboration, boration organo‐boron compounds
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description	Utilization of highly Lewis‐acidic boranes allows for transition metal‐free hydroboration of (hetero)aryl‐ and vinyl substituted terminal alkynes.
doi_str_mv	10.1002/chin.201636168
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subjects	alkenes (benzene compounds) e/z‐selectivity (incl. e/z‐isomerism) hydroboration, boration organo‐boron compounds
title	ChemInform Abstract: Highly Selective Catalytic trans‐Hydroboration of Alkynes Mediated by Borenium Cations and B(C6F5)3
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