These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
207 related articles for article (PubMed ID: 13229073)
1. [Historical points in the field of organic chemistry. II. Origin of the names given to compounds of the uric acid group by early authors; etymology of the term barbituric acid]. CATTELAIN E Ann Pharm Fr; 1954 Jun; 12(6):487-90. PubMed ID: 13229073 [No Abstract] [Full Text] [Related]
2. [Some historical points in the field of organic chemistry]. CATTELAIN E Ann Pharm Fr; 1954 May; 12(5):392-4. PubMed ID: 13189216 [No Abstract] [Full Text] [Related]
3. Nomenclature of organic chemistry. Definitive rules for section C. Characteristic groups containing carbon, hydrogen, oxygen, nitrogen, halogen, sulfur, selenium, and/or tellurium. Issued by the Commission on the Nomenclature of Organic Chemistry. Pure Appl Chem; 1965; 11(1):1-260. PubMed ID: 5871783 [No Abstract] [Full Text] [Related]
4. Studies on reactions of barbituric acid derivatives. II. Stereoisomers of 1-methyl-5-allyl-5-(2'-aminopropyl)-barbituric acid and related compounds. Konieczny M Arch Immunol Ther Exp (Warsz); 1968; 16(5):837-49. PubMed ID: 5709633 [No Abstract] [Full Text] [Related]
5. The synthesis and pharmacological activity of 5-ethyl-5-(3-hydroxy-1-methylbutyl)-barbituric acid. Dickert YJ; Shea PJ; McCarty LP J Med Chem; 1966 Mar; 9(2):249. PubMed ID: 5911809 [No Abstract] [Full Text] [Related]
6. [How do the chemists manage to name 3 new substances every day?]. Samuelsson K Lakartidningen; 1991 Jun; 88(25):2321-3. PubMed ID: 2062143 [No Abstract] [Full Text] [Related]
9. New symbolism for electron shifts in electronic theory. III. Applications to some stereospecific thermal reactions. Kaneko C Tokyo Ika Shika Daigaku Iyo Kizai Kenkyusho Hokoku; 1974; 8():1-7. PubMed ID: 4534352 [No Abstract] [Full Text] [Related]
10. A stereochemically accurate chemical substance database based on the systematic names of organic compounds. 1. Low molecular weight organic compounds. Araki K; Kaji M J Chem Inf Comput Sci; 1991 Aug; 31(3):363-74. PubMed ID: 1939394 [TBL] [Abstract][Full Text] [Related]
11. [The Wiswesser Line Notation for organic compounds]. Call L Pharm Unserer Zeit; 1980 Nov; 9(6):161-78. PubMed ID: 7454736 [No Abstract] [Full Text] [Related]
12. [Studies on lipids used as drugs. 5. Significance of the benzidine number with special reference to a comparison with the thiobarbiturate number and Kreis' test]. Kühn H; Horsch W Pharmazie; 1972 Sep; 27(9):563-9. PubMed ID: 5086351 [No Abstract] [Full Text] [Related]
13. IUPAC tentative rules for the nomenclature of organic chemistry: section E: fundamental stereochemistry. Biochim Biophys Acta; 1970 Apr; 208(1):1-44. PubMed ID: 5441210 [No Abstract] [Full Text] [Related]
19. [Derivatives of 6-aminopenicillanic acid. VI. Relations between structure and activity in the field of semisynthetic penicillins with broad spectrum activity]. Pifferi G; Timbal MT; Testa E Farmaco Sci; 1966 Sep; 21(9):611-23. PubMed ID: 5971372 [No Abstract] [Full Text] [Related]
20. [Origin of the name barbituric acid]. GOORMAGHTIGH N Belg Tijdschr Geneesk; 1950 Dec; 6(24):1138-9. PubMed ID: 14800861 [No Abstract] [Full Text] [Related] [Next] [New Search]