Producción Científica Profesorado

Phenylboronic Acid/CuSO4 as an Efficient Catalyst for the Synthesis of 1,4-Disubstituted-1,2,3-Triazoles from Terminal Acetylenes and Alkyl Azides



Rojas Lima, Susana

2015

José Emilio de la Cerda-Pedro, Susana Rojas-Lima, Rosa Santillan and Heraclio López-Ruiz*, Phenylboronic Acid/CuSO4 as an Efficient Catalyst for the Synthesis of 1,4-Disubstituted-1,2,3-Triazoles from Terminal Acetylenes and Alkyl Azides, J. Mex. Chem. Soc. 2015, 59(2), 130-136


Abstract


The synthesis of 1,4-disubstituted-1,2,3-triazoles from alkylazides and terminal alkynes at room temperature and under microwaveheating was attained using Cu(I), generated in-situ fromcopper(II) sulfate and phenylboronic acid, as catalyst. Twelve newtriazoles were obtained in moderate to good yields (53-98%), and theproducts were obtained by crystallization from the mixture reactionwithout further purification



Producto de Investigación




Artículos relacionados

Further insight into three center hydrogen bonding. Participation in tautomeric equilibria of hetero...

Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes

r-Alkylation of (S)-Asparagine with Self-Regeneration of the Stereogenic Center: Enantioselective Sy...

ChemInform Abstract: Facile Preparation of [4.4]Metacyclophane- and [5.5]Paracyclophane-Type Macrocy...

Furocoumarins of three species of the genus Dorstenia

The Structural Chemistry of N-Monolithium Borazines

Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles

A flexible access to highly functionalised boronates

Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles

Preparation of Seven- and Eight-Membered Boron Heterocycles from Different Salen Ligands and Arylbor...