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Advances in Catalytic Asymmetric Dearomatization

[Image: see text] Asymmetric catalysis has been recognized as the most enabling strategy for accessing chiral molecules in enantioenriched forms. Catalytic asymmetric dearomatization is an emerging and dynamic research subject in asymmetric catalysis, which has received considerable attention in rec...

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Detalles Bibliográficos
Autores principales: Zheng, Chao, You, Shu-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006174/
https://www.ncbi.nlm.nih.gov/pubmed/33791426
http://dx.doi.org/10.1021/acscentsci.0c01651
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author Zheng, Chao
You, Shu-Li
author_facet Zheng, Chao
You, Shu-Li
author_sort Zheng, Chao
collection PubMed
description [Image: see text] Asymmetric catalysis has been recognized as the most enabling strategy for accessing chiral molecules in enantioenriched forms. Catalytic asymmetric dearomatization is an emerging and dynamic research subject in asymmetric catalysis, which has received considerable attention in recent years. The direct transformations from readily available aromatic feedstocks to structurally diverse three-dimensional polycyclic molecules make catalytic asymmetric dearomatization reactions of broad interest for both organic synthesis and medicinal chemistry. However, the inherent difficulty for the disruption of aromaticity demands a large energy input during the dearomatization process, which might be incompatible with the conditions generally required by asymmetric catalysis. In this Outlook, we will discuss representative strategies and examples of catalytic asymmetric dearomatization reactions of various aromatic compounds and try to convince readers that by overcoming the above obstacles, catalytic asymmetric dearomatization reactions could advance chemical sciences in many respects.
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spelling pubmed-80061742021-03-30 Advances in Catalytic Asymmetric Dearomatization Zheng, Chao You, Shu-Li ACS Cent Sci [Image: see text] Asymmetric catalysis has been recognized as the most enabling strategy for accessing chiral molecules in enantioenriched forms. Catalytic asymmetric dearomatization is an emerging and dynamic research subject in asymmetric catalysis, which has received considerable attention in recent years. The direct transformations from readily available aromatic feedstocks to structurally diverse three-dimensional polycyclic molecules make catalytic asymmetric dearomatization reactions of broad interest for both organic synthesis and medicinal chemistry. However, the inherent difficulty for the disruption of aromaticity demands a large energy input during the dearomatization process, which might be incompatible with the conditions generally required by asymmetric catalysis. In this Outlook, we will discuss representative strategies and examples of catalytic asymmetric dearomatization reactions of various aromatic compounds and try to convince readers that by overcoming the above obstacles, catalytic asymmetric dearomatization reactions could advance chemical sciences in many respects. American Chemical Society 2021-02-22 2021-03-24 /pmc/articles/PMC8006174/ /pubmed/33791426 http://dx.doi.org/10.1021/acscentsci.0c01651 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Zheng, Chao
You, Shu-Li
Advances in Catalytic Asymmetric Dearomatization
title Advances in Catalytic Asymmetric Dearomatization
title_full Advances in Catalytic Asymmetric Dearomatization
title_fullStr Advances in Catalytic Asymmetric Dearomatization
title_full_unstemmed Advances in Catalytic Asymmetric Dearomatization
title_short Advances in Catalytic Asymmetric Dearomatization
title_sort advances in catalytic asymmetric dearomatization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006174/
https://www.ncbi.nlm.nih.gov/pubmed/33791426
http://dx.doi.org/10.1021/acscentsci.0c01651
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