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New Reactions of Contraction of the o-Quinone Ring with the Formation of Derivatives of 2-(2-Indolyl)-cyclopenta[b]pyrrole-3,4-diones and Pyrindino[1,2-a]indoles: A Combined Experimental and Density Functional Theory Investigation

[Image: see text] Derivatives of 2-(2-indolyl)-cyclopenta[b]pyrrole-3,4-diones and pyrindino[1,2-a]indoles were synthesized by a new reaction of contraction of the o-quinone ring, and their structures were investigated by X-ray crystallography and nuclear magnetic resonance spectroscopy. The mechani...

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Detalles Bibliográficos
Autores principales: Sayapin, Yurii A., Dorogan, Igor V., A. Gusakov, Evgeny, Bang, Duong Nghia, Tkachev, Valery V., Tupaeva, Inna Olegovna, Tran, Dai Lam, Nguyen, Trang Van, Duong, Toan Ngoc, Vu Dinh, Hoang, A. Krasnikova, Tatyana, M. Aldoshin, Serguei, Minkin, Vladimir I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296560/
https://www.ncbi.nlm.nih.gov/pubmed/34308053
http://dx.doi.org/10.1021/acsomega.1c02033
Descripción
Sumario:[Image: see text] Derivatives of 2-(2-indolyl)-cyclopenta[b]pyrrole-3,4-diones and pyrindino[1,2-a]indoles were synthesized by a new reaction of contraction of the o-quinone ring, and their structures were investigated by X-ray crystallography and nuclear magnetic resonance spectroscopy. The mechanisms of the reactions were suggested based on density functional theory calculations of the critical parts of the potential energy surfaces.