Regioselective Transition Metal-Free Catalytic Ring Opening of 2H-Azirines by Phenols and Naphthols; One-Pot Access to Benzo- and Naphthofurans

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Autor(es): dc.contributorUniversity of Calcutta-
Autor(es): dc.contributorCSIR-Central Drug Research Institute-
Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.contributorImam Abdulrahman Bin Faisal University-
Autor(es): dc.contributorUniversidade Estadual de Campinas (UNICAMP)-
Autor(es): dc.creatorRoy, Arnab-
Autor(es): dc.creatorBiswas, Subrata-
Autor(es): dc.creatorDuari, Surajit-
Autor(es): dc.creatorMaity, Srabani-
Autor(es): dc.creatorMishra, Abhishek Kumar-
Autor(es): dc.creatorSouza, Aguinaldo R. de-
Autor(es): dc.creatorElsharif, Asma M.-
Autor(es): dc.creatorMorgon, Nelson H.-
Autor(es): dc.creatorBiswas, Srijit-
Data de aceite: dc.date.accessioned2025-08-21T17:25:28Z-
Data de disponibilização: dc.date.available2025-08-21T17:25:28Z-
Data de envio: dc.date.issued2025-04-29-
Data de envio: dc.date.issued2023-11-16-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1021/acs.joc.3c01266-
Fonte completa do material: dc.identifierhttps://hdl.handle.net/11449/305696-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/305696-
Descrição: dc.descriptionBenzofuran and naphthofuran derivatives are synthesized from readily available phenols and naphthols. Regioselective ring openings of 2H-azirine followed by in situ aromatization using a catalytic amount of Brønsted acid have established the novelty of the methodology. The involvement of a series of 2H-azirines with a variety of phenols, 1-naphthols, and 2-naphthols showed the generality of the protocol. In-depth density functional theory calculations revealed the reaction mechanism with the energies of the intermediates and transition states of a model reaction. An alternate pathway of the mechanism has also been proposed with computer modeling.-
Descrição: dc.descriptionDepartment of Chemistry University of Calcutta, 92, A. P. C. Road, West Bengal-
Descrição: dc.descriptionDepartment of Medicinal and Process Chemistry CSIR-Central Drug Research Institute, Uttar Pradesh-
Descrição: dc.descriptionDepartment of Chemistry School of Science São Paulo State University, São Paulo-
Descrição: dc.descriptionDepartment of Chemistry Imam Abdulrahman Bin Faisal University-
Descrição: dc.descriptionDepartment of Physical Chemistry Institute of Chemistry Campinas State University, São Paulo-
Descrição: dc.descriptionDepartment of Chemistry School of Science São Paulo State University, São Paulo-
Formato: dc.format15580-15588-
Idioma: dc.languageen-
Relação: dc.relationJournal of Organic Chemistry-
???dc.source???: dc.sourceScopus-
Título: dc.titleRegioselective Transition Metal-Free Catalytic Ring Opening of 2H-Azirines by Phenols and Naphthols; One-Pot Access to Benzo- and Naphthofurans-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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