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SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols
A cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for forming allylic alcohols mediated by SO(2)F(2) was developed. This method provides a mild process for the preparation of allylic alcohol moieties witho...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072135/ https://www.ncbi.nlm.nih.gov/pubmed/35531509 http://dx.doi.org/10.1039/c9ra05346h |
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author | Jiang, Ying Alharbi, Njud S. Sun, Bing Qin, Hua-Li |
author_facet | Jiang, Ying Alharbi, Njud S. Sun, Bing Qin, Hua-Li |
author_sort | Jiang, Ying |
collection | PubMed |
description | A cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for forming allylic alcohols mediated by SO(2)F(2) was developed. This method provides a mild process for the preparation of allylic alcohol moieties without the requirement of transition metals. |
format | Online Article Text |
id | pubmed-9072135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90721352022-05-06 SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols Jiang, Ying Alharbi, Njud S. Sun, Bing Qin, Hua-Li RSC Adv Chemistry A cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for forming allylic alcohols mediated by SO(2)F(2) was developed. This method provides a mild process for the preparation of allylic alcohol moieties without the requirement of transition metals. The Royal Society of Chemistry 2019-09-20 /pmc/articles/PMC9072135/ /pubmed/35531509 http://dx.doi.org/10.1039/c9ra05346h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Jiang, Ying Alharbi, Njud S. Sun, Bing Qin, Hua-Li SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols |
title | SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols |
title_full | SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols |
title_fullStr | SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols |
title_full_unstemmed | SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols |
title_short | SO(2)F(2) mediated cascade dehydrogenative Morita–Baylis–Hillman reaction of the C(sp(3))–H of primary alcohols with the C(sp(2))–H of electron-deficient olefins for the assembly of allylic alcohols |
title_sort | so(2)f(2) mediated cascade dehydrogenative morita–baylis–hillman reaction of the c(sp(3))–h of primary alcohols with the c(sp(2))–h of electron-deficient olefins for the assembly of allylic alcohols |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072135/ https://www.ncbi.nlm.nih.gov/pubmed/35531509 http://dx.doi.org/10.1039/c9ra05346h |
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