Results 241 to 250 of about 5,049 (275)
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Study on Synthesis of Thebaine Derivatives
Chinese Journal of Chemistry, 2005The reaction of 7α-acetyl-6,14-endoethano-6,7,8,14-tetrahydrothebaine with 2-(thien-2-yl)ethylmagnesium bromide was investigated. The tertiary alcohol derivative 7α-[R-1-hydroxyl-1-methyl-3-(thien-2-yl)propyl])-6,14-endoethano-6,7,8,14-tetrahydrothebaine (3) and a by-product 4 were isolated. The structure of 4 was elucidated by X-ray analysis.
He Liu+4 more
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Reaction of thebaine with dinitrogen tetroxide
Journal of Heterocyclic Chemistry, 1979AbstractTreatment of thebaine with dinitrogen tetroxide gave a mixture of 14β‐nitrocodeinone (23%) and 8‐nitrothebaine (7%).
Sydney Archer, Peter Osei-Gyimah
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ChemInform Abstract: THEBAINE AND ACETYLENIC DIENOPHILES
Chemischer Informationsdienst, 1982AbstractThebain (1) reagiert mit Propiolsäuremethylester (II) in Methanol zu den beiden Addukten(I1I) und (IV).
A. SINGH+3 more
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Pharmacokinetics and Metabolism of [3H] Thebaine
Xenobiotica, 19741. A method is described for determination of [3H]thebaine in biological materials with sensitivity of 10–20 ng.2. Following a 5 mg/kg subcutaneous dose of [3H]thebaine to rats, max. brain and plasma concns. were 937 ng/g and 1076 ng/ml at 0.5 and 1 h, respectively; these declined to non-detectable levels at 24 h.
R B Pontani, A L Misra, S J Mulé
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Direct and Simple O-Demethylation of Thebaine to Oripavine
The Journal of Organic Chemistry, 1996AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Coop, A, Lewis, JW, Rice, KC
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Mikrobielle Umwandlung von Thebain
Experientia, 1969Thebaine was transformed into 2 products by fermentation with a strain ofTrametes cinnabarina. The 2 compounds were isolated and identified as 14-Β-hydroxycodeinone and 14-Β-hydroxycodeinone-N-oxid.
D. Gröger, H. P. Schmauder
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Chemische Berichte, 1967
AbstractBei der Öffnung des Piperidinringes im Thebain mit Acetyl‐ und Benzoylchlorid sowie Chlorameisensäure‐äthyl‐und ‐benzylester in feuchtem Äthylacetat entstehen die entsprechen‐den Codeinon‐acyl‐normethine (1a–1d), die je nach Katalyse interessante Umlagerungs‐und Spaltungsreaktionen eingehen.
Christa Bertgen+2 more
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AbstractBei der Öffnung des Piperidinringes im Thebain mit Acetyl‐ und Benzoylchlorid sowie Chlorameisensäure‐äthyl‐und ‐benzylester in feuchtem Äthylacetat entstehen die entsprechen‐den Codeinon‐acyl‐normethine (1a–1d), die je nach Katalyse interessante Umlagerungs‐und Spaltungsreaktionen eingehen.
Christa Bertgen+2 more
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Addition reaction of thebaine and β-dihydrothebaine with phenylsulphonylpropadiene
J. Chem. Soc., Chem. Commun., 1984AbstractThebain (I) reagiert mit Phenylsulfonylallen (II) zu einem untrennbaren Gemisch der Addukte (IIIa) und (IIIb), die bei der Hydrolyse nur ein Keton (IV) ergeben.
K. Ryu+3 more
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J. Chem. Soc. C, 1971
The reaction of thebaine with a number of 1,1-disubstituted ethylenes has been investigated; structures have been assigned to the adducts formed.
I. A. Selby+4 more
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The reaction of thebaine with a number of 1,1-disubstituted ethylenes has been investigated; structures have been assigned to the adducts formed.
I. A. Selby+4 more
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Colorimetric Determination of Thebaine in Papauer Bracteatum
Journal of Pharmaceutical Sciences, 1981A rapid colorimetric test for the determination of thebaine in dried, extracted Papaver bracteatum is described. The method is based on the development of an orange color formed by the nitroso color reaction for phenols. The absorption peak is near 450 nm. The linear range response is from 0 to 1.0 mg of thebaine.
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