Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9241
Title: Molecular complexity and diversity from aromatics. Intramolecular cycloaddition of cyclohexa-2,4-dienones and sigmatropic shift in excited state: a unified approach towards synthesis of polycyclic frameworks related to crotogoudin, conidiogenol, and crinipellins
Authors: Mobin, Shaikh M.
Keywords: aromatic compound;conidiogenol;crinipellin;crotogoudin;cyclohexa 2,4 dienone derivative;diterpenoid;unclassified drug;aromatization;Article;cycloaddition;Diels Alder reaction;oxidation;photoreactivity;priority journal;reaction analysis;synthesis
Issue Date: 2016
Publisher: Elsevier Ltd
Citation: Behera, T. K., Jarhad, D. B., Mobin, S. M., & Singh, V. (2016). Molecular complexity and diversity from aromatics. intramolecular cycloaddition of cyclohexa-2,4-dienones and sigmatropic shift in excited state: A unified approach towards synthesis of polycyclic frameworks related to crotogoudin, conidiogenol, and crinipellins. Tetrahedron, 72(35), 5377-5393. doi:10.1016/j.tet.2016.07.023
Abstract: Synthesis of polycyclic systems related to conidiogenol, crinipellin, and crotogoudin from simple aromatic precursor has been described. Oxidative dearomatization, tandem retro-Diels–Alder/Diels–Alder reaction, and photoreaction are the key features of our approach. © 2016 Elsevier Ltd
URI: https://doi.org/10.1016/j.tet.2016.07.023
https://dspace.iiti.ac.in/handle/123456789/9241
ISSN: 0040-4020
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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