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Steroidal alcohols

Jackpot see Fentanyl Jativa-M. see Salvia divinorum Jelly baby see Amphetamines Jet see Ketamine PCP (phencyclidine) Jet fuel see PCP (phencyclidine) Jolt see GBL Joy plant see Opium Jugs see Amphetamines Juice see Alcohol Steroids Junk see Steroids Leapers see Amphetamines Legal E see BenzylpiperazinelTrifluoromethylphenyl-piperazine Legal steroid see Creatine Legal X see BenzylpiperazinelTrifluoromethylphenyl-piperazine Lemon 714 see PCP (phencyclidine) Lemon fX drops see GHB Lethal weapon see PCP (phencyclidine) Liberty caps see Psilocybin Librium see Benzodiazepine... [Pg.499]

Harvey, D.J., Comparison of fourteen substituted silyl derivatives for the characterization of alcohols, steroids and cannabinoids by combined gas-liquid chromatography and mass spectrometry, J. Chromatogr., 147, 291, 1978. [Pg.97]

Figure 11.7 Schematic three-dimensional representation of the GABAa receptor complex with the recognition sites for GABA, benzodiazepines, alcohol, steroids, and barbiturates. Figure 11.7 Schematic three-dimensional representation of the GABAa receptor complex with the recognition sites for GABA, benzodiazepines, alcohol, steroids, and barbiturates.
Oxidation of allylic alcohols. Steroidal allylic alcohols are oxidized to the corresponding a,/3-unsaturated ketones in high yield by chromic anhydride in HMPT.2 The reaction is rapid in the case of equatorial alcohols but requires some weeks in the case of axial alcohols. Nonallylic hydroxyl groups are not affected. If the alcohol is only slightly soluble in HMPT, purified acetone is used as cosolvent. The reaction, if slow, can be carried out at 50°. Benzyl alcohol is oxidized, but in low yield (30%). [Pg.78]

Hydrophobic compounds are commonly considered to be those compounds extractable with immiscible semi- or non-polar organic solvents. Included in this group are long-chain fatty acids, fatty acid esters and waxes, long-chain alcohols, steroids, hydrocarbons, phospholipids and anthropogenic compounds (e.g. chlorinated hydrocarbons, oil hydrocarbons, phthalate esters). [Pg.475]

TCEP 7>/s-cyano ethoxy propane 175 Alcohols, Steroids, Pesticides... [Pg.693]

Used as silylation reagent for alcohols, steroids and sterols (gc-photoionization detn.). Oil. Bp3o 96°. [Pg.221]

Silylation reagent for use in gc anal, of alcohols, steroids and cannabinoids. Bp 99-100°. [Pg.427]

See other pages where Steroidal alcohols is mentioned: [Pg.764]    [Pg.765]    [Pg.358]    [Pg.247]    [Pg.228]    [Pg.405]    [Pg.845]    [Pg.101]    [Pg.244]    [Pg.46]    [Pg.165]    [Pg.87]    [Pg.95]    [Pg.366]    [Pg.540]    [Pg.235]    [Pg.32]    [Pg.429]    [Pg.913]    [Pg.149]    [Pg.384]    [Pg.218]    [Pg.87]    [Pg.190]   


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