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Substrate-Controlled Product Divergence: Silver-Catalyzed Reaction of Trifluoromethyl Ketones with Terminal Alkynes
[Image: see text] A distinct dichotomy in product distribution was initially observed in the silver-catalyzed reaction of trifluoromethyl (CF(3)) ketones with terminal alkynes having two different types of electronic natures. The domino reaction smoothly proceeded almost exclusively with high stereo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640928/ https://www.ncbi.nlm.nih.gov/pubmed/31457493 http://dx.doi.org/10.1021/acsomega.6b00432 |
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author | Li, Fang-Ling Wang, Lei Li, Cui-Hua Liu, Ning Dai, Bin |
author_facet | Li, Fang-Ling Wang, Lei Li, Cui-Hua Liu, Ning Dai, Bin |
author_sort | Li, Fang-Ling |
collection | PubMed |
description | [Image: see text] A distinct dichotomy in product distribution was initially observed in the silver-catalyzed reaction of trifluoromethyl (CF(3)) ketones with terminal alkynes having two different types of electronic natures. The domino reaction smoothly proceeded almost exclusively with high stereoselectivity with terminal alkynes containing ester groups, whereas alkynylation occurred in good yield when terminal alkynes containing aryl or alkyl groups were present. The results indicated that the electronic nature of terminal alkynes can act as a switch that enables either the domino reaction or alkynylation between terminal alkynes and CF(3) ketones. |
format | Online Article Text |
id | pubmed-6640928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66409282019-08-27 Substrate-Controlled Product Divergence: Silver-Catalyzed Reaction of Trifluoromethyl Ketones with Terminal Alkynes Li, Fang-Ling Wang, Lei Li, Cui-Hua Liu, Ning Dai, Bin ACS Omega [Image: see text] A distinct dichotomy in product distribution was initially observed in the silver-catalyzed reaction of trifluoromethyl (CF(3)) ketones with terminal alkynes having two different types of electronic natures. The domino reaction smoothly proceeded almost exclusively with high stereoselectivity with terminal alkynes containing ester groups, whereas alkynylation occurred in good yield when terminal alkynes containing aryl or alkyl groups were present. The results indicated that the electronic nature of terminal alkynes can act as a switch that enables either the domino reaction or alkynylation between terminal alkynes and CF(3) ketones. American Chemical Society 2017-03-22 /pmc/articles/PMC6640928/ /pubmed/31457493 http://dx.doi.org/10.1021/acsomega.6b00432 Text en Copyright © 2017 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 | Li, Fang-Ling Wang, Lei Li, Cui-Hua Liu, Ning Dai, Bin Substrate-Controlled Product Divergence: Silver-Catalyzed Reaction of Trifluoromethyl Ketones with Terminal Alkynes |
title | Substrate-Controlled Product Divergence: Silver-Catalyzed
Reaction of Trifluoromethyl Ketones with Terminal Alkynes |
title_full | Substrate-Controlled Product Divergence: Silver-Catalyzed
Reaction of Trifluoromethyl Ketones with Terminal Alkynes |
title_fullStr | Substrate-Controlled Product Divergence: Silver-Catalyzed
Reaction of Trifluoromethyl Ketones with Terminal Alkynes |
title_full_unstemmed | Substrate-Controlled Product Divergence: Silver-Catalyzed
Reaction of Trifluoromethyl Ketones with Terminal Alkynes |
title_short | Substrate-Controlled Product Divergence: Silver-Catalyzed
Reaction of Trifluoromethyl Ketones with Terminal Alkynes |
title_sort | substrate-controlled product divergence: silver-catalyzed
reaction of trifluoromethyl ketones with terminal alkynes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640928/ https://www.ncbi.nlm.nih.gov/pubmed/31457493 http://dx.doi.org/10.1021/acsomega.6b00432 |
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