Investigation of tartaric acid amide formation by thermolysis of tartaric acids with alkylamines

Significance of urinary tartaric acid.

Tartaric Acid Dehydrogenase Activity in Higher Plants1,2

Although the tartrates have been considered as possible metabolites in higher plants since the initial work of Pasteur in 1848, surprisingly little is known of their actual physiological significance. Vickery and Palmer (35) have briefly reviewed the history of (+)-tartrate in plants, including the problems of identification and of nomenclature. They conclude that (+)-tartrate is an uncommon pl...

l-Asparagine–l-tartaric acid (1/1)

In the title compound, C(4)H(8)N(2)O(3)·C(4)H(6)O(6), the amino acid mol-ecule exists as a zwitterion and the carb-oxy-lic acid in an un-ionized state. The tartaric acid mol-ecules are linked into layers parallel to the ab plane by O-H⋯O hydrogen bonds. The amino acid mol-ecules are also linked into layers parallel to the ab plane by N-H⋯O and C-H⋯O hydrogen bonds. The alternating tartaric acid...

Diastereoselective encapsulation of tartaric acid by a helical aromatic oligoamide.

A helical aromatic oligoamide foldamer encapsulates tartaric acid with exceptional affinity, selectivity, and diastereoselectivity. The structure of the complex has been elucidated both in solution by NMR spectroscopy and in the solid state by X-ray crystallography, making it possible to rationalize the strong effects observed, particularly the role of hydrogen bonds between the hydroxyl and ca...

Glycine–d-tartaric acid (1/1)

In the title co-crystal, C(2)H(5)NO(2)·C(4)H(6)O(6), the gylcine mol-ecule is present in the zwitterion form. In the tartaric acid mol-ecule there is a short intra-molecular O-H⋯O contact. In the crystal, the tartaric acid mol-ecules are linked via pairs of O-H⋯O hydrogen bonds, forming inversion dimers. These dimers are linked via a number of O-H⋯O and N-H⋯O hydrogen bonds involving the two co...