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.
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Ylidaddukte der Penteltrichloride
Bis(acetylsalicylato-j2O,O00)diaquacadmium(II)
Aroylthioureas: new organic ionophores for heavy-metal ion selective electrodes
Et3, and efficient Mediator for Xanthate Transfer Based Radical Processes.
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.