Intramolecular carbolithiation-cyclization-electrophilic substitution: Solvent effect and mechanistic study

The intramolecular carbolithiation-cyclization-electrophilic substitution sequence proves to be a promising strategy for synthetic organic chemists. Our current research in this area focuses on the one-pot halogen/lithium exchange of 2-bromophenyl-3-phenylprop-2-enyl ether, followed by intramolecula...

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Detalles Bibliográficos
Publicado:	2013
Materias:	Carbolithiation-cyclization-electrophilic substitution Conducted tour mechanism Inversion mechanism SE2 electrophilic substitution Solvent effect
Acceso en línea:	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v_n_p_Rodriguez http://hdl.handle.net/20.500.12110/paper_08943230_v_n_p_Rodriguez
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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