Azide-Enolate 1,3-Dipolar Cycloaddition as an Efficient Approach for the Synthesis of 1,5-Disubstituted 1,2,3-Triazoles from Alkyl/Aryl Azides and beta-Ketophosphonates
Por:
Gonzalez-Calderon, Davir, Fuentes-Benites, Aydee, Diaz-Torres, Eduardo, Gonzalez-Gonzalez, Carlos A., Gonzalez-Romero, Carlos
Publicada:
1 feb 2016
Resumen:
A simple procedure to prepare 1,5-disubstituted 1,2,3-triazoles
efficiently from alkyl/aryl azides and beta-ketophosphonates in the
presence of KOH by an azide-enolate 1,3-dipolar cycloaddition in good
yields was developed.
Filiaciones:
Gonzalez-Calderon, Davir:
Univ Autonoma Estado Mexico, Fac Quim, Dept Quim Organ, Paseo Colon Paseo Tollocan S-N, Toluca 50120, Estado De Mexic, Mexico
Fuentes-Benites, Aydee:
Univ Autonoma Estado Mexico, Fac Quim, Dept Quim Organ, Paseo Colon Paseo Tollocan S-N, Toluca 50120, Estado De Mexic, Mexico
Diaz-Torres, Eduardo:
Univ Nacl Autonoma Mexico, Inst Quim, Circuito Exterior S-N,Ciudad Univ, Mexico City 04510, DF, Mexico
Gonzalez-Gonzalez, Carlos A.:
Univ Autonoma Estado Mexico, Fac Quim, Dept Quim Organ, Paseo Colon Paseo Tollocan S-N, Toluca 50120, Estado De Mexic, Mexico
Gonzalez-Romero, Carlos:
Univ Autonoma Estado Mexico, Fac Quim, Dept Quim Organ, Paseo Colon Paseo Tollocan S-N, Toluca 50120, Estado De Mexic, Mexico
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