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...
Guardado en:
Autores principales: | Rodriguez, C., Nudelman, N.S. |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_08943230_v34_n4_p322_Rodriguez |
Aporte de: |
Ejemplares similares
-
Intramolecular carbolithiation-cyclization-electrophilic substitution: Solvent effect and mechanistic study
Publicado: (2014) -
Intramolecular carbolithiation-cyclization-electrophilic substitution: Solvent effect and mechanistic study
por: Rodriguez, C., et al. -
Intramolecular carbolithiation-cyclization-electrophilic substitution: Solvent effect and mechanistic study
Publicado: (2013) -
Synthesis of substituted benzofurans by the tandem one-pot intramolecular carbolithiation-cyclization-substitution sequence
por: Rodríguez, C., et al. -
Synthesis of substituted benzofurans by the tandem one-pot intramolecular carbolithiation-cyclization-substitution sequence
Publicado: (2014)