Producción Científica Profesorado

Synthesis of nitrogen-, oxygen- and sulphur-containing tripodal ligands with a trimethylbenzene core.



Lopez Ruíz, Heraclio

2011

López-Ruiz Heraclio,* Cortés-Hernández Mayra, Rojas- Lima Susana, Höpfl Herbert. Synthesis of nitrogen-, oxygen- and sulphur-containing tripodal ligands with a trimethylbenzene core. Journal of the Mexican Chemical Society, 55(3), 168-175. (2011)


Abstract


Synthetic procedures for the preparation of various nitrogen-, oxygen- and sulphur-containing tripodal ligands having a 1,3,5-trimethylbenzene core are reported.



Producto de Investigación




Artículos relacionados

Enantioselective synthesis of ?-amino acids. Part 11: Diastereoselective alkylation of chiral deriva...

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction

Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes

3-Benzoyl-2-isopropyl-4-alkyloxazolidin-5-ones as Efficient and Inexpensive Sources of Enantiopure ?...

Synthesis of New Chiral Derivatives of N,N?-Dimethylpropyleneurea (DMPU) and Examination of Their In...

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

An efficient potassium cyanide-promoted synthesis of 2-arylbenzoxazoles from [4.3.0]boron heterobicy...

Further insight into three center hydrogen bonding. Participation in tautomeric equilibria of hetero...

Diastereomeric C-glycosyloxanthrones from picramnia antidesma

Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.