Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles

The photo-induced denitrogenative annulations of a variety of 1-alkenylbenzotriazoles were investigated. By judiciously manipulating the structural variations of 1-alkenylbenzotriazoles, two characteristic polycyclic skeletons associated with monoterpene indole alkaloids were constructed through a d...

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Detalles Bibliográficos
Autores principales: Wang, Zhiguo, Chen, Yi, Dong, Zhen, Tang, Yefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823906/
https://www.ncbi.nlm.nih.gov/pubmed/36615557
http://dx.doi.org/10.3390/molecules28010363
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author Wang, Zhiguo
Chen, Yi
Dong, Zhen
Tang, Yefeng
author_facet Wang, Zhiguo
Chen, Yi
Dong, Zhen
Tang, Yefeng
author_sort Wang, Zhiguo
collection PubMed
description The photo-induced denitrogenative annulations of a variety of 1-alkenylbenzotriazoles were investigated. By judiciously manipulating the structural variations of 1-alkenylbenzotriazoles, two characteristic polycyclic skeletons associated with monoterpene indole alkaloids were constructed through a diverted and controllable manner. The present work not only enriches the photochemistry of 1-alkenylbenzotriazoles, but also offers a unified approach to access skeletally diverse indole alkaloid scaffolds.
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spelling pubmed-98239062023-01-08 Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles Wang, Zhiguo Chen, Yi Dong, Zhen Tang, Yefeng Molecules Article The photo-induced denitrogenative annulations of a variety of 1-alkenylbenzotriazoles were investigated. By judiciously manipulating the structural variations of 1-alkenylbenzotriazoles, two characteristic polycyclic skeletons associated with monoterpene indole alkaloids were constructed through a diverted and controllable manner. The present work not only enriches the photochemistry of 1-alkenylbenzotriazoles, but also offers a unified approach to access skeletally diverse indole alkaloid scaffolds. MDPI 2023-01-02 /pmc/articles/PMC9823906/ /pubmed/36615557 http://dx.doi.org/10.3390/molecules28010363 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Zhiguo
Chen, Yi
Dong, Zhen
Tang, Yefeng
Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles
title Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles
title_full Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles
title_fullStr Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles
title_full_unstemmed Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles
title_short Natural Product-Oriented Photo-Induced Denitrogenative Annulations of 1-Alkenylbenzotriazoles
title_sort natural product-oriented photo-induced denitrogenative annulations of 1-alkenylbenzotriazoles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823906/
https://www.ncbi.nlm.nih.gov/pubmed/36615557
http://dx.doi.org/10.3390/molecules28010363
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AT dongzhen naturalproductorientedphotoinduceddenitrogenativeannulationsof1alkenylbenzotriazoles
AT tangyefeng naturalproductorientedphotoinduceddenitrogenativeannulationsof1alkenylbenzotriazoles

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