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
Synthesis and Structures of some Lithium and Sodium (Aminoalcoholato)hydrido Aluminates
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles
A practical access to acyl radicals from acyl hydrazides
Synthesis of new homochiral 2,3-dialkylpiperazines derived from (R)-(?)-phenylglycinol
Structural studies of spiroarsoranes derived from 2-aminophenols
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.