103411-90-1Relevant articles and documents
Ozonolysis of alkenes and study of the reactions of polyfunctional compounds. XXXIV. Regiospecific synthesis of diastereomeric (+/-)-7,11-dimethyloctadecane and (+/-)-17,21-dimethylheptatriacontane
Odinokov, V. N.,Akhmetova, V. R.,Savchenko, R. G.,Vyrypaev, E. M.,Tolstikov, G. A.
, p. 71 - 74 (2007/10/02)
(Z,Z)-1,5-Dimethyl-1,5-cyclooctadiene upon partial ozonolysis with subsequent two-step olefination of the isoprenoid ketoaldehyde formed gives 8,12-dimethyl-4,8,12-octadecatriene and 17,21-dimethyl-13,17,21-heptatriacontatriene, whose hexahydro derivative
SYNTHESIS OF (-)-DIHYDROMAHUBANOLIDE B AND (-)-ISODIHYDROMAHUBANOLIDE B
Tanaka, Akira,Yamashita, Kyohei
, p. 319 - 322 (2007/10/02)
The total synthesis of (-)-dihydromahubanolide B and (-)-isodihydromahubanolide B isolated from the Amazonian Lauraceae Licaria mahuba (Samp.) Kosterm was achieved starting from (-)-methyl 5-hydroxymethyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate which was readily available from L-(+)-tartaric acid.