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A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes
We report a designed stereodivergent strategy for the synthesis of gem‐diborylcyclopropanes. The reaction provides a highly modular approach to prepare cyclopropane ring variants bearing gem‐(Bpin,Bpin), gem‐(Bpin,Bdan), and gem‐(Bpin,BF(3)K), with outstanding levels of stereocontrol. This was achie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092851/ https://www.ncbi.nlm.nih.gov/pubmed/36161797 http://dx.doi.org/10.1002/chem.202202748 |
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author | Hanania, Nicole Nassir, Molhm Eghbarieh, Nadim Masarwa, Ahmad |
author_facet | Hanania, Nicole Nassir, Molhm Eghbarieh, Nadim Masarwa, Ahmad |
author_sort | Hanania, Nicole |
collection | PubMed |
description | We report a designed stereodivergent strategy for the synthesis of gem‐diborylcyclopropanes. The reaction provides a highly modular approach to prepare cyclopropane ring variants bearing gem‐(Bpin,Bpin), gem‐(Bpin,Bdan), and gem‐(Bpin,BF(3)K), with outstanding levels of stereocontrol. This was achieved by diastereoselective Pd‐catalyzed cyclopropanation reactions of gem‐diborylalkenes with α‐diazoarylacetates and α‐diazoaryl‐trifluoromethyl. The key to the success of this general protocol was the diastereoselective trifluorination reaction of gem‐diborylcyclopropanes, followed by the stereospecific interconversion of the trifluoroborate salts into the Bdan group. |
format | Online Article Text |
id | pubmed-10092851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100928512023-04-13 A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes Hanania, Nicole Nassir, Molhm Eghbarieh, Nadim Masarwa, Ahmad Chemistry Research Articles We report a designed stereodivergent strategy for the synthesis of gem‐diborylcyclopropanes. The reaction provides a highly modular approach to prepare cyclopropane ring variants bearing gem‐(Bpin,Bpin), gem‐(Bpin,Bdan), and gem‐(Bpin,BF(3)K), with outstanding levels of stereocontrol. This was achieved by diastereoselective Pd‐catalyzed cyclopropanation reactions of gem‐diborylalkenes with α‐diazoarylacetates and α‐diazoaryl‐trifluoromethyl. The key to the success of this general protocol was the diastereoselective trifluorination reaction of gem‐diborylcyclopropanes, followed by the stereospecific interconversion of the trifluoroborate salts into the Bdan group. John Wiley and Sons Inc. 2022-10-31 2022-12-27 /pmc/articles/PMC10092851/ /pubmed/36161797 http://dx.doi.org/10.1002/chem.202202748 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Hanania, Nicole Nassir, Molhm Eghbarieh, Nadim Masarwa, Ahmad A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes |
title | A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes |
title_full | A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes |
title_fullStr | A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes |
title_full_unstemmed | A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes |
title_short | A Stereodivergent Approach to the Synthesis of gem‐Diborylcyclopropanes |
title_sort | stereodivergent approach to the synthesis of gem‐diborylcyclopropanes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092851/ https://www.ncbi.nlm.nih.gov/pubmed/36161797 http://dx.doi.org/10.1002/chem.202202748 |
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