Ácido heptatriacontanoico (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ácido heptatriacontanoico" in Galician language version.

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Rafidinarivo, Elie; Lanéelle, Marie-Antoinette; Montrozier, Henri; Pedro, Valero-Guillén; Astola, José; Luquin, Marina; Promé, Jean-Claude; Daffé, Mamadou (2008-09-04). "Trafficking pathways of mycolic acids: structures, origin, mechanism of formation, and storage form of mycobacteric acids" (PDF). The Journal of Lipid Research 50 (3): 477–490. PMID 18772482. doi:10.1194/jlr.M800384-JLR200. Consultado o 2014-04-22. En conxunto estes resultados estableceron a estrutura do maior homólogo de ácidos micobacterianos libres de M. brumae como un ácido 4,21-dimetil-5,19-di-(trans)-enoil-heptatriacontanoico.

US 5502226, Cho, Suk H. & DeFlorio, Victor, "Process of preparing ω-hydroxy acids", issued 1996-03-26

Rafidinarivo, Elie; Lanéelle, Marie-Antoinette; Montrozier, Henri; Pedro, Valero-Guillén; Astola, José; Luquin, Marina; Promé, Jean-Claude; Daffé, Mamadou (2008-09-04). "Trafficking pathways of mycolic acids: structures, origin, mechanism of formation, and storage form of mycobacteric acids" (PDF). The Journal of Lipid Research 50 (3): 477–490. PMID 18772482. doi:10.1194/jlr.M800384-JLR200. Consultado o 2014-04-22. En conxunto estes resultados estableceron a estrutura do maior homólogo de ácidos micobacterianos libres de M. brumae como un ácido 4,21-dimetil-5,19-di-(trans)-enoil-heptatriacontanoico.

Lai, X. Y.; Zhao, Y. Y.; Liang, H. (2006). "Studies on chemical constituents in flower of Abelmoschus manihot". China Journal of Chinese Materia Medica 31 (19): 1597–1600. PMID 17165583.
Rafidinarivo, Elie; Lanéelle, Marie-Antoinette; Montrozier, Henri; Pedro, Valero-Guillén; Astola, José; Luquin, Marina; Promé, Jean-Claude; Daffé, Mamadou (2008-09-04). "Trafficking pathways of mycolic acids: structures, origin, mechanism of formation, and storage form of mycobacteric acids" (PDF). The Journal of Lipid Research 50 (3): 477–490. PMID 18772482. doi:10.1194/jlr.M800384-JLR200. Consultado o 2014-04-22. En conxunto estes resultados estableceron a estrutura do maior homólogo de ácidos micobacterianos libres de M. brumae como un ácido 4,21-dimetil-5,19-di-(trans)-enoil-heptatriacontanoico.