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Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter
A practical sulfa-Michael/aldol cascade reaction of 1,4-dithiane-2,5-diol and α-aryl-β-nitroacrylates has been developed, which allows efficient access to functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter in moderate to good yields with high enantioselectivities.
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086683/ https://www.ncbi.nlm.nih.gov/pubmed/35548804 http://dx.doi.org/10.1039/c8ra04325f |
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author | Zhu, Xiao-Yu Lv, Mei-Heng Zhao, Ya-Nan Lan, Li-Yan Li, Wen-Ze Xiao, Lin-Jiu |
author_facet | Zhu, Xiao-Yu Lv, Mei-Heng Zhao, Ya-Nan Lan, Li-Yan Li, Wen-Ze Xiao, Lin-Jiu |
author_sort | Zhu, Xiao-Yu |
collection | PubMed |
description | A practical sulfa-Michael/aldol cascade reaction of 1,4-dithiane-2,5-diol and α-aryl-β-nitroacrylates has been developed, which allows efficient access to functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter in moderate to good yields with high enantioselectivities. |
format | Online Article Text |
id | pubmed-9086683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90866832022-05-10 Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter Zhu, Xiao-Yu Lv, Mei-Heng Zhao, Ya-Nan Lan, Li-Yan Li, Wen-Ze Xiao, Lin-Jiu RSC Adv Chemistry A practical sulfa-Michael/aldol cascade reaction of 1,4-dithiane-2,5-diol and α-aryl-β-nitroacrylates has been developed, which allows efficient access to functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter in moderate to good yields with high enantioselectivities. The Royal Society of Chemistry 2018-10-03 /pmc/articles/PMC9086683/ /pubmed/35548804 http://dx.doi.org/10.1039/c8ra04325f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhu, Xiao-Yu Lv, Mei-Heng Zhao, Ya-Nan Lan, Li-Yan Li, Wen-Ze Xiao, Lin-Jiu Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
title | Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
title_full | Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
title_fullStr | Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
title_full_unstemmed | Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
title_short | Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
title_sort | organocatalytic sulfa-michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086683/ https://www.ncbi.nlm.nih.gov/pubmed/35548804 http://dx.doi.org/10.1039/c8ra04325f |
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