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InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids

A novel polyene cyclization using the allene group as the initiator has been successfully developed. This methodology provides an efficient strategy for the construction of an abietane-type tricyclic skeleton with a functionalizable C2–C3 double bond and features a wide substrate scope and excellent...

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Autores principales: Huo, Chen-Yu, Zheng, Tian-Lu, Dai, Wei-Hao, Zhang, Zi-Hao, Wang, Jin-Da, Zhu, Dao-Yong, Wang, Shao-Hua, Zhang, Xiao-Ming, Xu, Xue-Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710309/
https://www.ncbi.nlm.nih.gov/pubmed/36544726
http://dx.doi.org/10.1039/d2sc04229k
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author Huo, Chen-Yu
Zheng, Tian-Lu
Dai, Wei-Hao
Zhang, Zi-Hao
Wang, Jin-Da
Zhu, Dao-Yong
Wang, Shao-Hua
Zhang, Xiao-Ming
Xu, Xue-Tao
author_facet Huo, Chen-Yu
Zheng, Tian-Lu
Dai, Wei-Hao
Zhang, Zi-Hao
Wang, Jin-Da
Zhu, Dao-Yong
Wang, Shao-Hua
Zhang, Xiao-Ming
Xu, Xue-Tao
author_sort Huo, Chen-Yu
collection PubMed
description A novel polyene cyclization using the allene group as the initiator has been successfully developed. This methodology provides an efficient strategy for the construction of an abietane-type tricyclic skeleton with a functionalizable C2–C3 double bond and features a wide substrate scope and excellent stereoselectivities. Potential utility of this approach has been well demonstrated by the collective total synthesis of seven abietane-type diterpenoids. Specifically, (±)-2,3-dihydroxyferruginol and (±)-2,3-dihydroxy-15,16-dinor-ent-pimar-8,11,13-triene were synthesized for the first time.
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spelling pubmed-97103092022-12-20 InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids Huo, Chen-Yu Zheng, Tian-Lu Dai, Wei-Hao Zhang, Zi-Hao Wang, Jin-Da Zhu, Dao-Yong Wang, Shao-Hua Zhang, Xiao-Ming Xu, Xue-Tao Chem Sci Chemistry A novel polyene cyclization using the allene group as the initiator has been successfully developed. This methodology provides an efficient strategy for the construction of an abietane-type tricyclic skeleton with a functionalizable C2–C3 double bond and features a wide substrate scope and excellent stereoselectivities. Potential utility of this approach has been well demonstrated by the collective total synthesis of seven abietane-type diterpenoids. Specifically, (±)-2,3-dihydroxyferruginol and (±)-2,3-dihydroxy-15,16-dinor-ent-pimar-8,11,13-triene were synthesized for the first time. The Royal Society of Chemistry 2022-11-02 /pmc/articles/PMC9710309/ /pubmed/36544726 http://dx.doi.org/10.1039/d2sc04229k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Huo, Chen-Yu
Zheng, Tian-Lu
Dai, Wei-Hao
Zhang, Zi-Hao
Wang, Jin-Da
Zhu, Dao-Yong
Wang, Shao-Hua
Zhang, Xiao-Ming
Xu, Xue-Tao
InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
title InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
title_full InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
title_fullStr InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
title_full_unstemmed InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
title_short InI(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
title_sort ini(3)-catalyzed polyene cyclization of allenes and its application in the total synthesis of seven abietane-type diterpenoids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710309/
https://www.ncbi.nlm.nih.gov/pubmed/36544726
http://dx.doi.org/10.1039/d2sc04229k
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