By G. Jones

Show description

Read Online or Download Chemistry of Triazolopyridines PDF

Similar chemistry books

Alkaloids: Chemical and Biological Perspectives, Vol. 15

Acronycine, a effective antitumor agent, was once stumbled on within the bark of the small Australian Rutaceous tree, Acronychia baueri Schott. This new paintings offers a entire survey of the isolation, constitution selection, equipment of synthesis, and the organic houses of acronycine, in addition to an account of average and artificial analogues of acronycine, and their organic houses.

Chemistry of Heterocyclic Compounds: Imidazole and Its Derivatives, Part I, Volume 6

Content material: bankruptcy I common homes and constitution of the Imidazoles (pages 3–31): bankruptcy II The Alkyl? and Arylimidazoles (pages 33–54): bankruptcy III The Oxo? and Hydroxyimidazoles and their Sulfur Analogues (pages 55–110): bankruptcy IV The Halogenoimidazoles (pages 111–125): bankruptcy V The Nitro? , Arylazo?

Extra resources for Chemistry of Triazolopyridines

Sample text

Daines, J. Med. Chem. 36, 3308 (1993). R. A. Daines, P. A. Chambers, I. Pendrak, D. R. Jakas, H. M. Sarau, J. J. Foley, D. B. Schmidt, and W. D. I. Med. Chem. 36, 3321 (1993). J. M. Amigo, L. Ochando, B. Abarca, R. Ballesteros, and J. Rius, Materials Science Forum 133-136, 201 (1993). M. Carcelli, L. Mavilla, C. Pelizzi, and G. Pelizzi, Spec. - R. Sot. Chem. 131, 121 (1993). E Albericio, L. A. Carpino, S. B. Daniels, A. El-Faham, H. Fukuda, G. U. Griffin, S. A. Kates, C. A. Minor, H. N. , Pept.

GURNOS JONES compound 310 gives improved quality in high temperature rapid processing (83GEP3438249), and compound 311 is a nucleation accelerator in direct positive colour photographic materials (88GEP3721570). Among catalysts for polymerization is 312 (98MIP40420). Compounds 4 and 5 have been used as corrosion inhibitors for copper (98MI7). Me / \ c ,Y= 2-J N-N $ a= OH 309 310 311 s N%x” hr 312 Ar = 2,6-(Pr’ NPh)&H3 REFERENCES 66CB2918 80EUP48555 8lBRPl588166 8 1BRP2054630 80JMS15 8lCC376 80MIl 8 1EUP25603 8 1FRP2450259 8lHCAll3 81IJC(B)lO 8lJOC3123 8lJAP(K)100783 81MIl 81MI2 8lMI3 8lMI4 M.

Arriau, J. Chem. , Perkin Trans. 2, 1317 (1983). F. Fabin, T. H. Dinh, and J. I. Golen, J. Heterocycl. Chem. 20, 1169 (1983). M. Bonamoni and L. Baiocchi, J. Hetemcycl. Chem. 20, 1657 (1983). C. Reichardt and E. Harbusch-Goernert, Justus Liebig’s Ann. , 721 (1983). B. Vercek, B. Ogorevc, B. Stanovnik, and M. Tisler, Monatsh. Chem. 114,789 (1983). B. Stanovnik, S. Podergajs, M. Tisler, and B. Vereek, Vestn. Slav. Dem. Drus 30, 39 (1983) [CA 99, 122348j (1983)]. L. Kaczmarek and P. Nantka-Namirski, Pal.

Download PDF sample

Rated 4.85 of 5 – based on 20 votes