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Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones
Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones have been established for the synthesis of enantioenriched γ-hydroxybutyric acid derivatives in the presence of Cu(ii)/trisoxazoline catalyst. These reactions offered the desired products in 70% to 93% yields with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990749/ https://www.ncbi.nlm.nih.gov/pubmed/36895764 http://dx.doi.org/10.1039/d2ra08257h |
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author | Zhang, Dongxin Chen, Lvjia Deng, Huiqing Zhang, Ying Cheng, Qihang Zhang, Qian-Feng |
author_facet | Zhang, Dongxin Chen, Lvjia Deng, Huiqing Zhang, Ying Cheng, Qihang Zhang, Qian-Feng |
author_sort | Zhang, Dongxin |
collection | PubMed |
description | Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones have been established for the synthesis of enantioenriched γ-hydroxybutyric acid derivatives in the presence of Cu(ii)/trisoxazoline catalyst. These reactions offered the desired products in 70% to 93% yields with 79% to 99% enantiomeric excesses. |
format | Online Article Text |
id | pubmed-9990749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-99907492023-03-08 Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones Zhang, Dongxin Chen, Lvjia Deng, Huiqing Zhang, Ying Cheng, Qihang Zhang, Qian-Feng RSC Adv Chemistry Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones have been established for the synthesis of enantioenriched γ-hydroxybutyric acid derivatives in the presence of Cu(ii)/trisoxazoline catalyst. These reactions offered the desired products in 70% to 93% yields with 79% to 99% enantiomeric excesses. The Royal Society of Chemistry 2023-03-07 /pmc/articles/PMC9990749/ /pubmed/36895764 http://dx.doi.org/10.1039/d2ra08257h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhang, Dongxin Chen, Lvjia Deng, Huiqing Zhang, Ying Cheng, Qihang Zhang, Qian-Feng Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
title | Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
title_full | Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
title_fullStr | Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
title_full_unstemmed | Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
title_short | Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
title_sort | asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990749/ https://www.ncbi.nlm.nih.gov/pubmed/36895764 http://dx.doi.org/10.1039/d2ra08257h |
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