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[BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres
Oxoborane carbamate and carboxylate analogues result from the in situ trapping of [BO(2)](−) produced by elimination of 2,3‐dimethyl‐2‐butene from a pinacolatoboryl anion.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496551/ https://www.ncbi.nlm.nih.gov/pubmed/32401402 http://dx.doi.org/10.1002/anie.202005674 |
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author | Pécharman, Anne‐Frédérique Hill, Michael S. McMullin, Claire L. Mahon, Mary F. |
author_facet | Pécharman, Anne‐Frédérique Hill, Michael S. McMullin, Claire L. Mahon, Mary F. |
author_sort | Pécharman, Anne‐Frédérique |
collection | PubMed |
description | Oxoborane carbamate and carboxylate analogues result from the in situ trapping of [BO(2)](−) produced by elimination of 2,3‐dimethyl‐2‐butene from a pinacolatoboryl anion. |
format | Online Article Text |
id | pubmed-7496551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74965512020-09-25 [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres Pécharman, Anne‐Frédérique Hill, Michael S. McMullin, Claire L. Mahon, Mary F. Angew Chem Int Ed Engl Communications Oxoborane carbamate and carboxylate analogues result from the in situ trapping of [BO(2)](−) produced by elimination of 2,3‐dimethyl‐2‐butene from a pinacolatoboryl anion. John Wiley and Sons Inc. 2020-06-04 2020-08-03 /pmc/articles/PMC7496551/ /pubmed/32401402 http://dx.doi.org/10.1002/anie.202005674 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Pécharman, Anne‐Frédérique Hill, Michael S. McMullin, Claire L. Mahon, Mary F. [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres |
title | [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres |
title_full | [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres |
title_fullStr | [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres |
title_full_unstemmed | [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres |
title_short | [BO(2)](−) as a Synthon for the Generation of Boron‐Centered Carbamate and Carboxylate Isosteres |
title_sort | [bo(2)](−) as a synthon for the generation of boron‐centered carbamate and carboxylate isosteres |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496551/ https://www.ncbi.nlm.nih.gov/pubmed/32401402 http://dx.doi.org/10.1002/anie.202005674 |
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