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Caron

Hydrolysis of cinenn I gives an optically active carboxylic acid (+) chrysanthemic acid Ozonolysis of (+) chrysanthemic acid followed by oxidation gives acetone and an optically active dicarboxyhc acid (—) caronic acid (C7H10O4) What is the struc ture of (—) caronic acid" Are the two carboxyl groups cis or trans to each other What does this information tell you about the structure of (+) chrysanthemic acid" ... [Pg.1105]

Tabac Blond (Caron 1919) Cuit de Russe (Chanel 1924)... [Pg.73]

English Lavender (Yardley 1770) Pour un Homme (Caron 1934) Eternity (Klein 1988)... [Pg.74]

Halston Z-14 (Halston 1976) Yatagan (Caron 1976) Adventurer (Bauer 1993) Sandahvood... [Pg.74]

John F. Breedis Ronald N. Caron Olin Corporation... [Pg.237]

Dalla Betta, Ralph A., Nicholas, S.G., Weakley, C.K., Lundberg, K., Caron, T.J., Chamberlain, J., and Greeb, K., Field Test of a 1.5 MW Industrial Gas Turbine with a Low Emissions Catalytic Combustion System, ASME 99-GT-295. [Pg.408]

Nancollas, G.H. and Reddy, M.M., 1971. The crystallization of calcium caronate. II Calcite growth mechanism. Journal of Colloid and Interfacial Science, 37, 824-833. [Pg.316]

Hydrobrotnic acid converts dihydrocarvone into a hydrobromide, CioHjyOBr, which, when treated with cold alcoholic potash, readily loses hydrogen bromide. Instead, however, of the unsaturated substance, -dihydrocarvone, being regenerated as the result of this decomposition, a remarkable formation of a c /cZopropane ring takes place and carone is produced—... [Pg.67]

Carone is then converted into its oxime, which is reduced by sodium and alcohol, and yields carylamine, Cj Hi-NH, which has the following constitution... [Pg.67]

Lefkowitz, R. J., Mullikin, D., and Caron, M. G. (1976). Regulation of P-adrenergic receptors by guanyl-5 -yl imidodiphosphate and other purine nucleotides. J. Biol. Chem. 251 4686-4692. [Pg.57]

As first described by Krizan and Martin,6 the in situ trapping protocol, i.e., having the base and electrophile present in solution simultaneously, makes it possible to lithiate substrates that are not applicable in classical ortho-lithiation reactions.7 Later, Caron and Hawkins utilized the compatibility of lithium diisopropylamide and triisopropyl borate to synthesize arylboronic acid derivatives of bulky, electron deficient neopentyl benzoic acid esters.8 As this preparation illustrates, the use of lithium tetramethylpiperidide instead of lithium diisopropylamide broadens the scope of the reaction, and makes it possible to functionalize a simple alkyl benzoate.2... [Pg.71]

Caron, A., and J. Donohue (1965) Bond lengths and thermal vibrations in orthorhombic sulfur. Acta Crystallogr. 18, 562-565. [Pg.622]

See other pages where Caron is mentioned: [Pg.84]    [Pg.661]    [Pg.355]    [Pg.309]    [Pg.199]    [Pg.260]    [Pg.29]    [Pg.72]    [Pg.284]    [Pg.285]    [Pg.72]    [Pg.136]    [Pg.136]    [Pg.461]    [Pg.94]    [Pg.1105]    [Pg.358]    [Pg.387]    [Pg.297]    [Pg.67]    [Pg.1103]    [Pg.583]    [Pg.78]    [Pg.145]    [Pg.709]    [Pg.442]    [Pg.71]    [Pg.617]    [Pg.344]    [Pg.168]    [Pg.606]    [Pg.1138]    [Pg.1272]    [Pg.1724]    [Pg.100]    [Pg.68]    [Pg.315]    [Pg.105]   
See also in sourсe #XX -- [ Pg.65 ]



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