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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...

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Detalles Bibliográficos
Autores principales: Hanania, Nicole, Nassir, Molhm, Eghbarieh, Nadim, Masarwa, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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