80685-82-1Relevant academic research and scientific papers
A NEW ROUTE FOR THE SYNTHESIS OF 10-HYDROXYDEC-2E-ENOIC AND DEC-2E-ENEDIOIC ACIDS
Odinokov, V. N.,Ishmuratov, G. Yu.,Tolstikov, G. A.
, p. 658 - 660 (1983)
A new simple route for the synthesis of 10-hydroxydec-2E-enoic and dec-2E-enedioic acids from cycloocta-1Z,5Z-diene has been developed.
A NOVEL STEREOSPECIFIC SYNTHESIS OF MUSCALURE, THE SEX PHEROMONE OF HOUSE FLY (MUSCA DOMESTICA)
Odinokov, V.N.,Tolstikov, G.A.,Galeyeva, R.I.,Kargapol'tseva, T.A.
, p. 1371 - 1372 (2007/10/02)
Partial ozonolysis of 1Z,5Z-cyclooctadiene followed by selective transformations of ester and acetal groups in methyl ester of 8,8-dimethoxy-4Z-octen-1-oic acid, and by a two step elongation of carbon chain of the latter by means of tosyloxy groups replacement under action of decyl- and pentyl magnesium bromides leads to muscalure - the sex pheromone of house fly.
PROSTANOIDS. II. SIMPLE METHOD FOR THE PRODUCTION OF CYCLOPENTENE SYNTHONS FROM 1,5-CYCLOOCTADIENE
Tolstikov, G. A.,Miftakhov, M. S.,Sidorov, N. N.,Valeev, F. A.,Odinokov, V. N.
, p. 499 - 503 (2007/10/02)
Simple methods are developed for the production of the synthons for prostaglandins by reaction of morpholinocyclopentene with ω-aldehydo acids.A covenient method is proposed for the conversion of 1,5-cyclooctadiene into 2-(5-methoxycarbonyl-2Z-pentenyl)-2-cyclopenten-1-one.
PROSTANOIDS. USE OF THE PRODUCTS FROM OZONOLYSIS OF CYCLIC OLEFINS AND DIENES IN THE SYNTHESIS OF SYNTHONS FOR PROSTAGLANDINS
Tolstikov, G. A.,Odinokov, V. N.,Miftakhov, M. S.,Galeeva, R. I.,Valeev, F. A.,et al.
, p. 627 - 632 (2007/10/02)
A method was developed for the synthesis of the esters of oxocarboxylic and dicarboxylic acids of the aliphatic series containing di- or trisubstituted double bonds with a specific Z or E configuration at a given point in the hydrocarbon chain by selective ozonolysis of cyclic olefins and dienes.
