Dearomative [3 + 2] cycloaddition reaction of nitrobenzothiophenes with nonstabilized azomethine ylides

A highly diastereoselective dearomative [3 + 2] 1,3-dipolar cycloaddition reaction of nitrobenzothiophenes with an in situ-generated nonstabilized azomethine ylides has been developed. The transformation provides a series of functionalized fused tricyclic benzo[4,5]thieno[2,3-c]pyrroles in good yiel...

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Detalles Bibliográficos
Autores principales: Wang, Kai-Kai, Xie, Yan-Xin, Li, Yan-Li, Chen, Rongxiang, Wang, Zhan-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055820/
https://www.ncbi.nlm.nih.gov/pubmed/35520074
http://dx.doi.org/10.1039/d0ra05687a

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055820/
https://www.ncbi.nlm.nih.gov/pubmed/35520074
http://dx.doi.org/10.1039/d0ra05687a

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