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-13-12764
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.
Preparation of N-aryl-substituted spiro-?-lactams via Staudinger cycloaddition
Et3, and efficient Mediator for Xanthate Transfer Based Radical Processes.
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles