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Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives
A highly enantioselective Michael addition reaction of anthrone with nitroalkenes by chiral tetraoxacalix[2]arene[2]triazine catalysts was investigated as a novel topic. The stereoselective conversion progressed smoothly by employing 10 mol% of the catalyst and afforded the corresponding Michael add...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065986/ https://www.ncbi.nlm.nih.gov/pubmed/35515554 http://dx.doi.org/10.1039/c9ra03029h |
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author | Genc, Hayriye Nevin |
author_facet | Genc, Hayriye Nevin |
author_sort | Genc, Hayriye Nevin |
collection | PubMed |
description | A highly enantioselective Michael addition reaction of anthrone with nitroalkenes by chiral tetraoxacalix[2]arene[2]triazine catalysts was investigated as a novel topic. The stereoselective conversion progressed smoothly by employing 10 mol% of the catalyst and afforded the corresponding Michael adducts with acceptable to high enantioselectivities (up to 97% ee) and very high yields (up to 96%). |
format | Online Article Text |
id | pubmed-9065986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90659862022-05-04 Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives Genc, Hayriye Nevin RSC Adv Chemistry A highly enantioselective Michael addition reaction of anthrone with nitroalkenes by chiral tetraoxacalix[2]arene[2]triazine catalysts was investigated as a novel topic. The stereoselective conversion progressed smoothly by employing 10 mol% of the catalyst and afforded the corresponding Michael adducts with acceptable to high enantioselectivities (up to 97% ee) and very high yields (up to 96%). The Royal Society of Chemistry 2019-07-05 /pmc/articles/PMC9065986/ /pubmed/35515554 http://dx.doi.org/10.1039/c9ra03029h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Genc, Hayriye Nevin Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
title | Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
title_full | Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
title_fullStr | Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
title_full_unstemmed | Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
title_short | Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
title_sort | enantioselective michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065986/ https://www.ncbi.nlm.nih.gov/pubmed/35515554 http://dx.doi.org/10.1039/c9ra03029h |
work_keys_str_mv | AT genchayriyenevin enantioselectivemichaelreactionofanthronecatalyzedbychiraltetraoxacalix2arene2triazinederivatives |