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
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles
Phenylmethyl 2,3,4-tri-O-acetyl--D-fucopyranoside
Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes
Synthesis and Structures of some Lithium and Sodium (Aminoalcoholato)hydrido Aluminates
Structural studies of spiroarsoranes derived from 2-aminophenols