Scientific Production Faculty

A Cu[I] catalyzed mild and general synthesis of 1,4-disubstituted-1,2,3-triazoles from terminal acetylenes and in situ generated alkyl azides.



Lopez Ruiz, Heraclio

2014

A Cu[I] catalyzed mild and general synthesis of 1,4-disubstituted-1,2,3-triazoles from terminal acetylenes and in situ generated alkyl azides. José Emilio de la Cerda-Pedro, Yoarhy Alejandro Amador-Sánchez, Mayra Cortés-Hernández, Jovana Pérez-Pérez, Susana Rojas-Lima and Heraclio López-Ruiz,Heterocycles 89, 27-41 (2014). DOI: 10.3987/COM-13-12764.


Abstract


Cuprous cyanide, generated in situ from cupric sulfate and sodium cyanide, catalyzes the synthesis of 1,4-disubstituted-1,2,3-triazoles from in situ generated alkyl azides and mono-substituted alkynes in a one pot room temperature process.



Research Product




Related articles

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

Effect of TiO2Al2O3 SolGel Supports on the Superficial Ni and Mo Species in Oxidized and Sulfided Ni...

A practical access to acyl radicals from acyl hydrazides

Cathepsins X and B Can Be Differentiated through Their Respective Mono- and Dipeptidyl Carboxypeptid...

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

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

Highly diastereoselective alkylation, acylation and aldol condensation of cis- and trans-(N-acyloyl)...

Facile synthesis of 1,3,6-oxadiazepines from 2,2?-(1,2-ethanediyldiimino)bisphenols

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

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio