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Lewis Acid-Catalyzed Enantioselective Friedel–Crafts Alkylation of Pyrrole in Water
[Image: see text] Highly enantioselective Friedel–Crafts alkylation of pyrroles with 2-enoyl-pyridine N-oxides in water/chloroform (10:1) was developed under catalysis of Lewis acid. The Friedel–Crafts alkylation products can be obtained in high yields and excellent enantioselectivities. Moreover, s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271029/ https://www.ncbi.nlm.nih.gov/pubmed/32548375 http://dx.doi.org/10.1021/acsomega.9b04115 |
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author | Sun, Jianan Gui, Yang Huang, Yekai Li, Jindong Zha, Zhenggen Yang, Yu Wang, Zhiyong |
author_facet | Sun, Jianan Gui, Yang Huang, Yekai Li, Jindong Zha, Zhenggen Yang, Yu Wang, Zhiyong |
author_sort | Sun, Jianan |
collection | PubMed |
description | [Image: see text] Highly enantioselective Friedel–Crafts alkylation of pyrroles with 2-enoyl-pyridine N-oxides in water/chloroform (10:1) was developed under catalysis of Lewis acid. The Friedel–Crafts alkylation products can be obtained in high yields and excellent enantioselectivities. Moreover, several control experiments were carried out to study the reaction mechanism. |
format | Online Article Text |
id | pubmed-7271029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-72710292020-06-15 Lewis Acid-Catalyzed Enantioselective Friedel–Crafts Alkylation of Pyrrole in Water Sun, Jianan Gui, Yang Huang, Yekai Li, Jindong Zha, Zhenggen Yang, Yu Wang, Zhiyong ACS Omega [Image: see text] Highly enantioselective Friedel–Crafts alkylation of pyrroles with 2-enoyl-pyridine N-oxides in water/chloroform (10:1) was developed under catalysis of Lewis acid. The Friedel–Crafts alkylation products can be obtained in high yields and excellent enantioselectivities. Moreover, several control experiments were carried out to study the reaction mechanism. American Chemical Society 2020-05-11 /pmc/articles/PMC7271029/ /pubmed/32548375 http://dx.doi.org/10.1021/acsomega.9b04115 Text en Copyright © 2020 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 | Sun, Jianan Gui, Yang Huang, Yekai Li, Jindong Zha, Zhenggen Yang, Yu Wang, Zhiyong Lewis Acid-Catalyzed Enantioselective Friedel–Crafts Alkylation of Pyrrole in Water |
title | Lewis Acid-Catalyzed Enantioselective Friedel–Crafts
Alkylation of Pyrrole in Water |
title_full | Lewis Acid-Catalyzed Enantioselective Friedel–Crafts
Alkylation of Pyrrole in Water |
title_fullStr | Lewis Acid-Catalyzed Enantioselective Friedel–Crafts
Alkylation of Pyrrole in Water |
title_full_unstemmed | Lewis Acid-Catalyzed Enantioselective Friedel–Crafts
Alkylation of Pyrrole in Water |
title_short | Lewis Acid-Catalyzed Enantioselective Friedel–Crafts
Alkylation of Pyrrole in Water |
title_sort | lewis acid-catalyzed enantioselective friedel–crafts
alkylation of pyrrole in water |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271029/ https://www.ncbi.nlm.nih.gov/pubmed/32548375 http://dx.doi.org/10.1021/acsomega.9b04115 |
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