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Chemoselective Boronic Ester Synthesis by Controlled Speciation**

Control of boronic acid solution speciation is presented as a new strategy for the chemoselective synthesis of boronic esters. Manipulation of the solution equilibria within a cross-coupling milieu enables the formal homologation of aryl and alkenyl boronic acid pinacol esters. The generation of a n...

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Autores principales: Fyfe, James W B, Seath, Ciaran P, Watson, Allan J B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501314/
https://www.ncbi.nlm.nih.gov/pubmed/25267096
http://dx.doi.org/10.1002/anie.201406714
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author Fyfe, James W B
Seath, Ciaran P
Watson, Allan J B
author_facet Fyfe, James W B
Seath, Ciaran P
Watson, Allan J B
author_sort Fyfe, James W B
collection PubMed
description Control of boronic acid solution speciation is presented as a new strategy for the chemoselective synthesis of boronic esters. Manipulation of the solution equilibria within a cross-coupling milieu enables the formal homologation of aryl and alkenyl boronic acid pinacol esters. The generation of a new, reactive boronic ester in the presence of an active palladium catalyst also facilitates streamlined iterative catalytic C=C bond formation and provides a method for the controlled oligomerization of sp(2)-hybridized boronic esters.
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spelling pubmed-45013142015-07-21 Chemoselective Boronic Ester Synthesis by Controlled Speciation** Fyfe, James W B Seath, Ciaran P Watson, Allan J B Angew Chem Int Ed Engl Communications Control of boronic acid solution speciation is presented as a new strategy for the chemoselective synthesis of boronic esters. Manipulation of the solution equilibria within a cross-coupling milieu enables the formal homologation of aryl and alkenyl boronic acid pinacol esters. The generation of a new, reactive boronic ester in the presence of an active palladium catalyst also facilitates streamlined iterative catalytic C=C bond formation and provides a method for the controlled oligomerization of sp(2)-hybridized boronic esters. WILEY-VCH Verlag 2014-11-03 2014-09-29 /pmc/articles/PMC4501314/ /pubmed/25267096 http://dx.doi.org/10.1002/anie.201406714 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Fyfe, James W B
Seath, Ciaran P
Watson, Allan J B
Chemoselective Boronic Ester Synthesis by Controlled Speciation**
title Chemoselective Boronic Ester Synthesis by Controlled Speciation**
title_full Chemoselective Boronic Ester Synthesis by Controlled Speciation**
title_fullStr Chemoselective Boronic Ester Synthesis by Controlled Speciation**
title_full_unstemmed Chemoselective Boronic Ester Synthesis by Controlled Speciation**
title_short Chemoselective Boronic Ester Synthesis by Controlled Speciation**
title_sort chemoselective boronic ester synthesis by controlled speciation**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501314/
https://www.ncbi.nlm.nih.gov/pubmed/25267096
http://dx.doi.org/10.1002/anie.201406714
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