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Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis
Unsymmetrical 1,1-bis(boryl)alkanes and alkenes are organo-bismetallic equivalents, which are synthetically important because they allow for sequential selective transformations of C–B bonds. We reviewed the synthesis and chemical reactivity of 1,1-bis(boryl)alkanes and alkenes to provide informatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070756/ https://www.ncbi.nlm.nih.gov/pubmed/32093409 http://dx.doi.org/10.3390/molecules25040959 |
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author | Babu, K. Naresh Massarwe, Fedaa Reddy, Reddy Rajasekhar Eghbarieh, Nadim Jakob, Manuella Masarwa, Ahmad |
author_facet | Babu, K. Naresh Massarwe, Fedaa Reddy, Reddy Rajasekhar Eghbarieh, Nadim Jakob, Manuella Masarwa, Ahmad |
author_sort | Babu, K. Naresh |
collection | PubMed |
description | Unsymmetrical 1,1-bis(boryl)alkanes and alkenes are organo-bismetallic equivalents, which are synthetically important because they allow for sequential selective transformations of C–B bonds. We reviewed the synthesis and chemical reactivity of 1,1-bis(boryl)alkanes and alkenes to provide information for the synthetic community. In the first part of this review, we disclose the synthesis and chemical reactivity of unsymmetrical 1,1-bisborylalkanes. In the second part, we describe the synthesis and chemical reactivity of unsymmetrical 1,1-bis(boryl)alkenes. |
format | Online Article Text |
id | pubmed-7070756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70707562020-03-19 Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis Babu, K. Naresh Massarwe, Fedaa Reddy, Reddy Rajasekhar Eghbarieh, Nadim Jakob, Manuella Masarwa, Ahmad Molecules Review Unsymmetrical 1,1-bis(boryl)alkanes and alkenes are organo-bismetallic equivalents, which are synthetically important because they allow for sequential selective transformations of C–B bonds. We reviewed the synthesis and chemical reactivity of 1,1-bis(boryl)alkanes and alkenes to provide information for the synthetic community. In the first part of this review, we disclose the synthesis and chemical reactivity of unsymmetrical 1,1-bisborylalkanes. In the second part, we describe the synthesis and chemical reactivity of unsymmetrical 1,1-bis(boryl)alkenes. MDPI 2020-02-20 /pmc/articles/PMC7070756/ /pubmed/32093409 http://dx.doi.org/10.3390/molecules25040959 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Babu, K. Naresh Massarwe, Fedaa Reddy, Reddy Rajasekhar Eghbarieh, Nadim Jakob, Manuella Masarwa, Ahmad Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis |
title | Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis |
title_full | Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis |
title_fullStr | Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis |
title_full_unstemmed | Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis |
title_short | Unsymmetrical 1,1-Bisboryl Species: Valuable Building Blocks in Synthesis |
title_sort | unsymmetrical 1,1-bisboryl species: valuable building blocks in synthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070756/ https://www.ncbi.nlm.nih.gov/pubmed/32093409 http://dx.doi.org/10.3390/molecules25040959 |
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