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A-Cedrene oxide

Cyclic ethers used as fragrances include a number of terpenoid compounds. Some of them, such as 1,4-cineole [470-67-7] and 1,8-cineole, occur in essential oils in significant quantities. Others are only minor components examples are rose oxide, ner-ol oxide [1786-08-9], and rose furan [15186-51-3], which contribute to the specific fragrance of rose oil. Caryophyllene oxide [1139-30-6], which has a woody, slightly ambergris-like odor, can be prepared by treatment of -caryophyllene with organic peracids. a-Cedrene oxide [11000-57-0] is another wood-fragrance compound, which can be easily prepared by epoxidation of cedarwood oil hydrocarbons. [Pg.149]

Carbon suboxide, 52 Carbonylation, 148, 149, 216 Carbonyl chlorofluoride, 48, 54 Carbonyl cyanide, 60-61 N,N -Carbonyldiimidazole, 61 1,1-Carbonyldi-l,2,4-triazole, 61 N-Carbonylsulfamic acid chloride (N-Carbonylsulfamyl chloride), 61 Carboxamides, 270 Carboxamine-N-sulfochlorides, 70 p-Carboxybenzenediazonium chloride, 62 p-Carboxybenzenesulfonazide, 62 Carboxylation, 15, 16 Carboxylic acid anhydrides, 133 Carboxylic acid N,N-dimethylamines, 153 Carboxylic anhydrides, 409-410 p-Carboxyphenylhydrazones, 62 Cardenolides, 130, 131 (S-Carotene, 19 /-Carvone, 451, 452 i//-Caryophyllene, 149, 150 Catechol, 65, 233 Catechol amines, 159 Catechyl phosphorus tribromide, 63 Catechyl phosphorus trichloride, 63 Cis-Cecropia juvenile hormone, 261 Cedrene, 234, 235 a-Cedrene, 349 /3-Cedrene, 349 Cendranoxide, 234, 235 Cephalosporin C, 48 Ceric ammonium nitrate, 63-65 Ceric sulfate. 65 Cesium fluoride, 346 trans-Chalcone oxide, 422 Chalcone phenylhydrazones, 257, 258 Chalcones, 406 Chloramine, 65-66, 69 Chloranil, 66-67, 113, 116, 401,454... [Pg.261]

Takigawa, H., H. Kubota, H. Sonohara, M. Okuda, S. Tanaka, Y. Fujikura, and S. Ito. 1993. Novel allylic oxidation of a-cedrene to sec-cedrenol by a RJiodococcus strain. Appl. Environ. Microbiol. 59 1336-1341. [Pg.684]

Carvone oxide CarvyI acetate L-CarvyI acetate Caryophyllene alcohol Caryophyllene alcohol acetate Cascara (Rhamnus purshiana) extract Castoreum Cedarwood oil Cedrene a-Cedrene 8-Cedrene epoxide Cedrenol... [Pg.5320]

Spathulenol, juniper camphor, chamazulene, P-caryophyllene, P-caryophyllene alcohol, caryophyllene oxide, chrysartemin A+B, a-cedrene, elemol, clovandiol, eudesmanolides... [Pg.93]

Nicotiana. The comprehensive study mentioned already above (see Sect. 7.2.1.1) demonstrated also the occurrence of Cj VOCs, i.e., sesquiterpenes e.g., p-caryophyllene (Fig. 7.4), a-cedrene, different famesenes (Fig. 7.4), a-humulene and oxygenated sesquiterpenes (e.g., different cis-trans isomers of nerolidol, far-nesal, and famesol, as well as caryophyllene oxide) (Raguso et al. 2003). Further constitutive sesquiterpenoids from Nicotiana will be discussed below in connection with phytoalexins of this genus. [Pg.349]

In addition. Green and Pettus have reported efficient syntheses of a-cedrene, a-pipitzol, and ec-cedrenol on the basis of a novel domino oxidative dearomatization-intramolecular [5+2] cycloaddition-acetic acid addition reaction [96]. Indeed, the key step of the syntheses began with the oxidative dearomatization of ortAo-(pent-4-enyl)-phenols 92, followed by an intramolecular [5+2] cycloaddition of the respective phenoxonium intermediate across the tethered olefin to afford the corresponding tricyclo-[5.3.1.0 ]-undecanes, which finally added acetic acid to provide the final products 93 in low to good yields, as shown in Scheme 20.40. The benzylic... [Pg.651]

Stereocenter effectively guided the formation of the first two stereocenters during the [5+2] reaction. The sequence then terminated with the selective incorporation of acetic acid to generate a third stereocenter, setting it apart from other previous cationic [5+2] reactions. It must be noted that this oxidative dearomatization-induced cascade reaction is unique as it proceeds in the absence of para-oxygen substituent. Starting from tricyclic product 93, the three members of the cedranoid family, a-cedrene, a-pipitzol, and ec-cedrenol, were easily achieved in several supplementary steps. [Pg.652]

Semmler and Risse have studied the oxidation of cedrene by means of ozone. They obtained the keto-acid, Cj Hj Oj, which on further oxidation either by means of bromine or nitric acid yields a dicarboxylic acid. [Pg.96]


See other pages where A-Cedrene oxide is mentioned: [Pg.142]    [Pg.280]    [Pg.301]    [Pg.142]    [Pg.280]    [Pg.301]    [Pg.78]    [Pg.88]    [Pg.89]    [Pg.625]    [Pg.164]    [Pg.165]    [Pg.120]    [Pg.324]    [Pg.74]    [Pg.658]    [Pg.660]    [Pg.658]    [Pg.660]   
See also in sourсe #XX -- [ Pg.142 ]

See also in sourсe #XX -- [ Pg.149 ]




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