BIOMAT Database Logo BIOMAT Database Logo

[Syntheses of oxazolecarboxylic acid derivatives. XII. Hydrogenolysis of aminoxazoles. (5). Syntheses of alkenylureas (author's transl)]. 1976

C Tanaka, and T Kurauchi, and M Nishida

UI MeSH Term Description Entries
D010080 Oxazoles Five-membered heterocyclic ring structures containing an oxygen in the 1-position and a nitrogen in the 3-position, in distinction from ISOXAZOLES where they are at the 1,2 positions. Oxazole,1,3-Oxazolium-5-Oxides,Munchnones,1,3 Oxazolium 5 Oxides
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D006859 Hydrogen The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas. Protium,Hydrogen-1
D000475 Alkenes Unsaturated hydrocarbons of the type Cn-H2n, indicated by the suffix -ene. (Grant & Hackh's Chemical Dictionary, 5th ed, p408) Alkene,Olefin,Olefins,Pentene,Pentenes
D014508 Urea A compound formed in the liver from ammonia produced by the deamination of amino acids. It is the principal end product of protein catabolism and constitutes about one half of the total urinary solids. Basodexan,Carbamide,Carmol

Related Publications

C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. XV. Hydrogenolysis of aminoxazoles. (8). Mechanism of the hydrogenolysis of 2-aminoxazoles (author's transl)].
May 1978, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. XI. Hydrogenolysis of aminoxazoles. (4). Syntheses and hydrogenolysis of 4- and 5-aminoxazoles].
April 1971, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. 8. Hydrogenolysis of aminoxazoles. 2].
January 1967, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. VII. Hydrogenolysis of aminoxazoles. (1)].
January 1967, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. XIII. Hydrogenolysis of aminoxazoles. (6). Syntheses and hydrogenolysis of 2-amino-2-oxazolines (author's transl)].
February 1977, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. XVI. Hydrogenolysis of aminoxazoles. (9). Effect of the amount of catalyst on the hydrogenolysis of 2-aminoxazoles (author's transl)].
January 1979, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. X. Hydrogenolysis of aminoxazoles. (3). Hydrogenolysis of alkyl, aralkyl, or aryl substituted 2-aminoxazoles].
April 1971, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. XIV. Hydrogenolysis of aminoxazoles. (7) Investigation on hydrogenolysis of benzyl 2-oxazolecarbamates by gas chromatography (author's transl)].
May 1978, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid derivatives. IX. Syntheses of alkyl, aralkyl, or aryl substituted 2-aminoxazoles].
April 1971, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and T Kurauchi, and M Nishida
[Syntheses of oxazolecarboxylic acid dervatives. IV. Syntheses of 5- or 6-oxazole-carboxylic acids and aminoxazoles].
January 1962, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
Copied contents to your clipboard!