Producción Científica Profesorado

Phenylboronic Acid/CuSO4 as an Efficient Catalyst for the Synthesis of1,4-Disubstituted-1,2,3-Triazoles from Terminal Acetylenes and Alkyl Azides



Lopez Ruíz, Heraclio

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

O-benzyl-N-(2-furoyl)thiocarbamate

Enantioselective synthesis of ?-amino acids. Part 11: Diastereoselective alkylation of chiral deriva...

Synthesis and Study of Isomeric Benzo[1,4]oxazines and Benzothiazolines by NMR Spectroscopy and X-Ra...

Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole d...

Structural studies of spiroarsoranes derived from 2-aminophenols

Comparative Structural Characterization of the Biquaternized N-CH3 and N-BH3 Derivatives of the cis-...

A practical access to acyl radicals from acyl hydrazides

New boronates prepared from 2,4-pentanedione derived ligands of the NO2 and N2O2 type comparison to...

Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.

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