Producción Científica Profesorado

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.



Rojas Lima, Susana

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 y Heraclio López-Ruiz,Heterocycles 89, 27-41 (2014). DOI: 10.3987/COM-13-12764http://www.heterocycles.jp/newlibrary/payments/form/23418/PDF


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.



Producto de Investigación




Artículos relacionados

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

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

Ylidaddukte der Penteltrichloride

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

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction

Structural studies of spiroarsoranes derived from 2-aminophenols

Synthesis and Study of Monomeric and Dimeric Boronates by Spectroscopic Methods and X-ray Crystallog...

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

A flexible access to highly functionalised boronates

Addition reaction of benzylbenzylidenenamine to lithium enolates of 1,3-dioxolan-4-one: synthesis of...