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

Rojas Lima, Susana

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

Artículos relacionados

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

Diastereomeric C-glycosyloxanthrones from picramnia antidesma

r-Alkylation of (S)-Asparagine with Self-Regeneration of the Stereogenic Center: Enantioselective Sy...

X-ray crystallographic study of neutral boron chelates with ?-diketones and tropolone

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

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

Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole d...

Ylidaddukte der Penteltrichloride

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

Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction