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Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies

[Image: see text] H(8)–BINOL, a partially reduced form of BINOL, is widely employed in a broad array of organocatalyzed asymmetric methodologies. Over the last 25 years, asymmetric organocatalysis has witnessed an incredible improvement, and an advancement still continues to get a single enantio-enr...

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Autor principal: Kshatriya, Rajpratap
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10210047/
https://www.ncbi.nlm.nih.gov/pubmed/37251114
http://dx.doi.org/10.1021/acsomega.2c05535
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author Kshatriya, Rajpratap
author_facet Kshatriya, Rajpratap
author_sort Kshatriya, Rajpratap
collection PubMed
description [Image: see text] H(8)–BINOL, a partially reduced form of BINOL, is widely employed in a broad array of organocatalyzed asymmetric methodologies. Over the last 25 years, asymmetric organocatalysis has witnessed an incredible improvement, and an advancement still continues to get a single enantio-enriched product. The broad-spectrum applications of H(8)–BINOL organocatalyst in C–C bond formation, C-heteroatom bond construction, name reactions, pericyclic reactions, and one pot and multicomponent reaction are attracting the attention of researchers. A diversified unique H(8)–BINOL-based catalyst has been synthesized and screened for catalytic activity. In this Review we frame out the H(8)–BINOL catalyzed novel discoveries from the last two decades.
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spelling pubmed-102100472023-05-26 Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies Kshatriya, Rajpratap ACS Omega [Image: see text] H(8)–BINOL, a partially reduced form of BINOL, is widely employed in a broad array of organocatalyzed asymmetric methodologies. Over the last 25 years, asymmetric organocatalysis has witnessed an incredible improvement, and an advancement still continues to get a single enantio-enriched product. The broad-spectrum applications of H(8)–BINOL organocatalyst in C–C bond formation, C-heteroatom bond construction, name reactions, pericyclic reactions, and one pot and multicomponent reaction are attracting the attention of researchers. A diversified unique H(8)–BINOL-based catalyst has been synthesized and screened for catalytic activity. In this Review we frame out the H(8)–BINOL catalyzed novel discoveries from the last two decades. American Chemical Society 2023-05-11 /pmc/articles/PMC10210047/ /pubmed/37251114 http://dx.doi.org/10.1021/acsomega.2c05535 Text en © 2023 The Author. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/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 Kshatriya, Rajpratap
Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies
title Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies
title_full Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies
title_fullStr Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies
title_full_unstemmed Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies
title_short Recent Advancement in H(8)–BINOL Catalyzed Asymmetric Methodologies
title_sort recent advancement in h(8)–binol catalyzed asymmetric methodologies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10210047/
https://www.ncbi.nlm.nih.gov/pubmed/37251114
http://dx.doi.org/10.1021/acsomega.2c05535
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