BIOMAT Database Logo BIOMAT Database Logo

[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)]. 1979

C Tanaka, and S Kuriyama

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
D010165 Palladium A chemical element having an atomic weight of 106.4, atomic number of 46, and the symbol Pd. It is a white, ductile metal resembling platinum, and following it in abundance and importance of applications. It is used in dentistry in the form of gold, silver, and copper alloys.
D010984 Platinum A heavy, soft, whitish metal, resembling tin, with atomic number 78, atomic weight 195.084, symbol Pt. It is used in manufacturing equipment for laboratory and industrial use. It occurs as a black powder (platinum black) and as a spongy substance (spongy platinum) and may have been known in Pliny's time as "alutiae". Platinum Black
D002244 Carbon A nonmetallic element with atomic symbol C, atomic number 6, and atomic weight [12.0096; 12.0116]. It may occur as several different allotropes including DIAMOND; CHARCOAL; and GRAPHITE; and as SOOT from incompletely burned fuel. Carbon-12,Vitreous Carbon,Carbon 12,Carbon, Vitreous
D002384 Catalysis The facilitation of a chemical reaction by material (catalyst) that is not consumed by the reaction. Catalyses

Related Publications

C Tanaka, and S Kuriyama
[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 S Kuriyama
[Syntheses of oxazolecarboxylic acid derivatives. 8. Hydrogenolysis of aminoxazoles. 2].
January 1967, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and S Kuriyama
[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 S Kuriyama
[Syntheses of oxazolecarboxylic acid derivatives. XII. Hydrogenolysis of aminoxazoles. (5). Syntheses of alkenylureas (author's transl)].
August 1976, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and S Kuriyama
[Syntheses of oxazolecarboxylic acid derivatives. VII. Hydrogenolysis of aminoxazoles. (1)].
January 1967, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
C Tanaka, and S Kuriyama
[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 S Kuriyama
[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 S Kuriyama
[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 S Kuriyama
[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 S Kuriyama
[SYNTHESES OF OXAZOLECARBOXYLIC ACID DERIVATIVES. VI. DECARBOXYLATION OF 2-OXAZOLECARBOXYLIC ACIDS].
March 1965, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
Copied contents to your clipboard!