10395-46-7Relevant articles and documents
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Kropp,P.J.
, p. 4926 - 4934 (1966)
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MECHANISM OF REARRANGEMENT WITH CYCLOPROPYL INVOLVEMENT IN ACETYLOSIS OF β-3,4-EPOXYCARANE
Arbuzov, B. A.,Isaeva, Z. G.,D'yakonova, R. R.
, p. 1949 - 1951 (1980)
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Monoterpenediol insect repellents
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, (2008/06/13)
An insect repellent comprising as an active ingredient a monoterpenediol compound having the formula, STR1 wherein R1, R2 and R3 have either one of the following definitions: (i) all of R1, R2 and R3 are hydrogen, (ii) R1 is hydrogen and R2 and R3, taken together, form a carbon-carbon single bond, or (iii) R2 is hydrogen, R1 and R3, taken together, form a carbon-carbon single bond, and the hydroxyl bonded to the carbon atom marked with an asterisk takes an α-configuration.
Transformations of 3-carene oxide at rhenium-containing catalysts
Manukov, E. N.,Bazhina, G. N.
, p. 106 - 110 (2007/10/02)
The transformations of 3-carene oxide at rhenium-containing catalysts were studied.The introduction of rhenium into the catalytic system significantly increases the reaction rate and leads to the formation of compounds not previously encountered in the products from the isomerization of 3-carene oxide, i.e., 3-carene, 3(10),4-caradiene, 3,3,6-trimethylcycloheptanone, and 3-caren-10-ol.
STEREOCHEMISTRY OF THE CARANE SYSTEM. OXIDATION PRODUCTS OF ISOMERIC 3,4-CARANEDIOLS OBTAINED FROM (+)-3-CARENE
Hendrich, Aleksandra,Piatkowski, Krzysztof
, p. 73 - 84 (2007/10/02)
Oxidation of four isomeric 3,4-caranediols has been carried out and reaction products have been investigated.It has been found that cis-diols rather form cyclic ketals than are oxidized under conditions of the Jones reaction.The key intermediate for syntheses of chrysanthemic acid, (-)-2-acetonyl-3,3-dimethylcyclopropaneacetic acid was obtained exclusively by oxidation of (-)-3β,4α-caranediol.