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.
A flexible access to highly functionalised boronates
Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters
Furocoumarins of three species of the genus Dorstenia
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles