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Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes
[Image: see text] The sulfenylation of the vinyl C–H bond in ketene dithioacetals leading to the synthesis of polythiolated alkenes is achieved via the promotion of molecular iodine. In addition, alkyl thiols also exhibit tolerance to the C–H bond elaboration reaction for the synthesis of correspond...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645039/ https://www.ncbi.nlm.nih.gov/pubmed/31459275 http://dx.doi.org/10.1021/acsomega.8b01946 |
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author | Deng, Leiling Liu, Yunyun |
author_facet | Deng, Leiling Liu, Yunyun |
author_sort | Deng, Leiling |
collection | PubMed |
description | [Image: see text] The sulfenylation of the vinyl C–H bond in ketene dithioacetals leading to the synthesis of polythiolated alkenes is achieved via the promotion of molecular iodine. In addition, alkyl thiols also exhibit tolerance to the C–H bond elaboration reaction for the synthesis of corresponding alkylthiolated ketene dithioacetals. |
format | Online Article Text |
id | pubmed-6645039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66450392019-08-27 Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes Deng, Leiling Liu, Yunyun ACS Omega [Image: see text] The sulfenylation of the vinyl C–H bond in ketene dithioacetals leading to the synthesis of polythiolated alkenes is achieved via the promotion of molecular iodine. In addition, alkyl thiols also exhibit tolerance to the C–H bond elaboration reaction for the synthesis of corresponding alkylthiolated ketene dithioacetals. American Chemical Society 2018-09-25 /pmc/articles/PMC6645039/ /pubmed/31459275 http://dx.doi.org/10.1021/acsomega.8b01946 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Deng, Leiling Liu, Yunyun Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes |
title | Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation
of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes |
title_full | Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation
of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes |
title_fullStr | Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation
of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes |
title_full_unstemmed | Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation
of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes |
title_short | Metal-Free Vinyl C–H Sulfenylation/Alkyl Thiolation
of Ketene Dithioacetals for the Synthesis of Polythiolated Alkenes |
title_sort | metal-free vinyl c–h sulfenylation/alkyl thiolation
of ketene dithioacetals for the synthesis of polythiolated alkenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645039/ https://www.ncbi.nlm.nih.gov/pubmed/31459275 http://dx.doi.org/10.1021/acsomega.8b01946 |
work_keys_str_mv | AT dengleiling metalfreevinylchsulfenylationalkylthiolationofketenedithioacetalsforthesynthesisofpolythiolatedalkenes AT liuyunyun metalfreevinylchsulfenylationalkylthiolationofketenedithioacetalsforthesynthesisofpolythiolatedalkenes |