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.
Artículos relacionados
The Structural Chemistry of N-Monolithium Borazines
A flexible access to highly functionalised boronates
O-benzyl-N-(2-furoyl)thiocarbamate
A practical access to acyl radicals from acyl hydrazides
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes