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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...

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Autores principales: Li, Fang-Ling, Wang, Lei, Li, Cui-Hua, Liu, Ning, Dai, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
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.
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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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