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Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress

Dehydroabietane-type bifunctional organocatalysts derived from rosane-type diterpenes of dehydroabietic acid (DHAA) and dehydroabietylamine (DA) have been utilized in a wide variety of highly enantioselective reactions. Since one well-documented review exclusively reported on the development of terp...

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Autores principales: Zhang, Zhen-Wei, Liu, Shao-Wu, Huang, Hong-Ping, Xie, Yu-Hang, Huang, Ruo-Chen, Deng, Yan-Qiu, Lin, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594059/
https://www.ncbi.nlm.nih.gov/pubmed/37881754
http://dx.doi.org/10.1039/d3ra06715g
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author Zhang, Zhen-Wei
Liu, Shao-Wu
Huang, Hong-Ping
Xie, Yu-Hang
Huang, Ruo-Chen
Deng, Yan-Qiu
Lin, Ning
author_facet Zhang, Zhen-Wei
Liu, Shao-Wu
Huang, Hong-Ping
Xie, Yu-Hang
Huang, Ruo-Chen
Deng, Yan-Qiu
Lin, Ning
author_sort Zhang, Zhen-Wei
collection PubMed
description Dehydroabietane-type bifunctional organocatalysts derived from rosane-type diterpenes of dehydroabietic acid (DHAA) and dehydroabietylamine (DA) have been utilized in a wide variety of highly enantioselective reactions. Since one well-documented review exclusively reported on the development of terpene-derived bifunctional thioureas in asymmetric organocatalysis in 2013, fragmentary progress on the dehydroabietane-type bifunctional thioureas and squaramides has been mentioned in other reviews. In this mini-review, we systematically analyze and reorganize the published literature on dehydroabietane-type bifunctional organocatalysts in the recent decade according to the type of catalysts. Our aim is for this review to provide helpful research information and serve as a foundation for further design and application of rosin-based organocatalysts.
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spelling pubmed-105940592023-10-25 Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress Zhang, Zhen-Wei Liu, Shao-Wu Huang, Hong-Ping Xie, Yu-Hang Huang, Ruo-Chen Deng, Yan-Qiu Lin, Ning RSC Adv Chemistry Dehydroabietane-type bifunctional organocatalysts derived from rosane-type diterpenes of dehydroabietic acid (DHAA) and dehydroabietylamine (DA) have been utilized in a wide variety of highly enantioselective reactions. Since one well-documented review exclusively reported on the development of terpene-derived bifunctional thioureas in asymmetric organocatalysis in 2013, fragmentary progress on the dehydroabietane-type bifunctional thioureas and squaramides has been mentioned in other reviews. In this mini-review, we systematically analyze and reorganize the published literature on dehydroabietane-type bifunctional organocatalysts in the recent decade according to the type of catalysts. Our aim is for this review to provide helpful research information and serve as a foundation for further design and application of rosin-based organocatalysts. The Royal Society of Chemistry 2023-10-24 /pmc/articles/PMC10594059/ /pubmed/37881754 http://dx.doi.org/10.1039/d3ra06715g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Zhen-Wei
Liu, Shao-Wu
Huang, Hong-Ping
Xie, Yu-Hang
Huang, Ruo-Chen
Deng, Yan-Qiu
Lin, Ning
Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
title Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
title_full Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
title_fullStr Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
title_full_unstemmed Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
title_short Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
title_sort dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594059/
https://www.ncbi.nlm.nih.gov/pubmed/37881754
http://dx.doi.org/10.1039/d3ra06715g
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