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

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

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

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

3-Benzoyl-2-isopropyl-4-alkyloxazolidin-5-ones as Efficient and Inexpensive Sources of Enantiopure ?...

Addition reaction of benzylbenzylidenenamine to lithium enolates of1,3-dioxolan-4-one: synthesis of ...

Synthesis and Structures of some Lithium and Sodium (Aminoalcoholato)hydrido Aluminates

Diastereomeric C-glycosyloxanthrones from picramnia antidesma

Enantioselective synthesis of ?-amino acids. Part 10: Preparation of novel ?,?- and ?,?-disubstitute...

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

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction