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Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement

New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement products.

Detalles Bibliográficos
Autores principales: Tancock, James, Wirth, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272767/
https://www.ncbi.nlm.nih.gov/pubmed/26076108
http://dx.doi.org/10.3390/molecules200610866
Descripción
Sumario:New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement products.