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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Chemical Society
2023
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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. |
format | Online Article Text |
id | pubmed-10210047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kshatriyarajpratap recentadvancementinh8binolcatalyzedasymmetricmethodologies |