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

Et3, and efficient Mediator for Xanthate Transfer Based Radical Processes.

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

Phenylmethyl 2,3,4-tri-O-acetyl--D-fucopyranoside

Aroylthioureas: new organic ionophores for heavy-metal ion selective electrodes

A flexible access to highly functionalised boronates

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio

Diastereomeric C-glycosyloxanthrones from picramnia antidesma

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

A practical access to acyl radicals from acyl hydrazides

Synthesis of nitrogen-, oxygen- and sulphur-containing tripodal ligands with a trimethylbenzene core...