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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2014
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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. |
format | Online Article Text |
id | pubmed-4501314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
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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