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Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols

Copper-catalyzed cross-coupling reactions of vinyl epoxide with arylboronates to obtain aryl-substituted homoallylic alcohols are described. The reaction selectivity was different to that of previously reported vinyl epoxide ring-opening reactions using aryl nucleophiles. The reaction proceeded unde...

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Detalles Bibliográficos
Autores principales: Lu, Xiao-Yu, Li, Jin-Song, Wang, Jin-Yu, Wang, Shi-Qun, Li, Yue-Ming, Zhu, Yu-Jing, Zhou, Ran, Ma, Wen-Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092012/
https://www.ncbi.nlm.nih.gov/pubmed/35559282
http://dx.doi.org/10.1039/c8ra09048c
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author Lu, Xiao-Yu
Li, Jin-Song
Wang, Jin-Yu
Wang, Shi-Qun
Li, Yue-Ming
Zhu, Yu-Jing
Zhou, Ran
Ma, Wen-Jing
author_facet Lu, Xiao-Yu
Li, Jin-Song
Wang, Jin-Yu
Wang, Shi-Qun
Li, Yue-Ming
Zhu, Yu-Jing
Zhou, Ran
Ma, Wen-Jing
author_sort Lu, Xiao-Yu
collection PubMed
description Copper-catalyzed cross-coupling reactions of vinyl epoxide with arylboronates to obtain aryl-substituted homoallylic alcohols are described. The reaction selectivity was different to that of previously reported vinyl epoxide ring-opening reactions using aryl nucleophiles. The reaction proceeded under mild conditions, affording aryl-substituted homoallylic alcohols with high selectivity and in good to excellent yields. The reaction provides convenient access to aryl-substituted homoallylic alcohols from vinyl epoxide
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spelling pubmed-90920122022-05-11 Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols Lu, Xiao-Yu Li, Jin-Song Wang, Jin-Yu Wang, Shi-Qun Li, Yue-Ming Zhu, Yu-Jing Zhou, Ran Ma, Wen-Jing RSC Adv Chemistry Copper-catalyzed cross-coupling reactions of vinyl epoxide with arylboronates to obtain aryl-substituted homoallylic alcohols are described. The reaction selectivity was different to that of previously reported vinyl epoxide ring-opening reactions using aryl nucleophiles. The reaction proceeded under mild conditions, affording aryl-substituted homoallylic alcohols with high selectivity and in good to excellent yields. The reaction provides convenient access to aryl-substituted homoallylic alcohols from vinyl epoxide The Royal Society of Chemistry 2018-12-12 /pmc/articles/PMC9092012/ /pubmed/35559282 http://dx.doi.org/10.1039/c8ra09048c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Lu, Xiao-Yu
Li, Jin-Song
Wang, Jin-Yu
Wang, Shi-Qun
Li, Yue-Ming
Zhu, Yu-Jing
Zhou, Ran
Ma, Wen-Jing
Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
title Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
title_full Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
title_fullStr Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
title_full_unstemmed Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
title_short Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
title_sort cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092012/
https://www.ncbi.nlm.nih.gov/pubmed/35559282
http://dx.doi.org/10.1039/c8ra09048c
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