Results 241 to 250 of about 44,738 (325)
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Organic Preparations and Procedures International, 1979
(1979). RECOMMENDED SYNTHESES FOR 7–METHYLBENZ[a]ANTHRACENE, 12–METHYLBENZ[a]ANTHRACENE AND 7,12–DIMETHYLBENZ[a]ANTHRACENE. Organic Preparations and Procedures International: Vol. 11, No. 6, pp. 271-274.
Melvin S. Newman +2 more
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(1979). RECOMMENDED SYNTHESES FOR 7–METHYLBENZ[a]ANTHRACENE, 12–METHYLBENZ[a]ANTHRACENE AND 7,12–DIMETHYLBENZ[a]ANTHRACENE. Organic Preparations and Procedures International: Vol. 11, No. 6, pp. 271-274.
Melvin S. Newman +2 more
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Anthracene 1,2-oxide: synthesis and role in the metabolism of anthracene by mammals
Journal of the Chemical Society, Perkin Transactions 1, 1979Synthesis of anthracene 1,2-oxide proceeds in good yield via dehydrobromination of 1 -acetoxy-2,4-dibromo1,2,3,4-tetrahydroanthracene. In contrast, dehydrobromination of 2-acetoxy-3,4-dibromo-1,2,3,4-tetrahydroanthracene produced 1 -bromoanthracene instead of the desired anthracene 2,3-oxide or its oxepin tautomer.
M N, Akhtar +5 more
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Biochemical Pharmacology, 1991
Benz[a]anthracene (BA) and the monomethyl meso-anthracenic or L-region derivatives 7-methylbenz[a]anthracene (7-methylBA) and 12-methylbenz[a]anthracene (12-methylBA) underwent a bioalkylation substitution reaction in rat lung ctyosol preparations, fortified with S-adenosyl-L-methionine to form the more potent carcinogen 7,12-dimethylbenz[a]anthracene.
S R, Myers, J W, Flesher
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Benz[a]anthracene (BA) and the monomethyl meso-anthracenic or L-region derivatives 7-methylbenz[a]anthracene (7-methylBA) and 12-methylbenz[a]anthracene (12-methylBA) underwent a bioalkylation substitution reaction in rat lung ctyosol preparations, fortified with S-adenosyl-L-methionine to form the more potent carcinogen 7,12-dimethylbenz[a]anthracene.
S R, Myers, J W, Flesher
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Thermoelectroluminescence in Anthracene and Anthracene Doped With Acridine Phosphors
Macromolecular SymposiaAbstractIn the present study, an effort is made to record the thermoelectroluminescence (TEL) glow curves and electroluminescence (EL) spectra for anthracene, acridine, and anthracene doped with acridine to determine the trap depth and escape frequency in these materials.
Ajai Kumar Mishra +2 more
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Synthesis of New Anthracene Derivatives
The Journal of Organic Chemistry, 2006An efficient synthesis is described for hexabromoanthracenes 3 and 4 by direct bromination of 9,10-dibromoanthrecene 2. Whereas base-induced elimination of hexabromide 3 with t-BuOK gave 2,3,9,10-tetrabromoanthracene 5, the reaction of hexabromide 4 with DBU afforded 1,3,9,10-tetrabromoanthracene 6 as the sole product.
Osman, Cakmak +3 more
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ChemInform Abstract: ANTHRACEN‐CYANAT UND ANTHRACEN‐OXAZINONE
Chemischer Informationsdienst. Organische Chemie, 1970AbstractDas aus dem Hydroxy‐anthracen (I) und BrCN in Aceton in Gegenwart von Triäthylamin dargestellte Cyanat (II) gibt in saurer, wäßriger Lösung das Carbamat (III), mit H2S das Thiocarbamat (IV).
MIR HEDAYATULLAH +2 more
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Radiation Induced Paramagnetic Centers in Anthracene and Deuterated Anthracene
Molecular Crystals, 1968Abstract EPR Studies of radiation damage in anthracene C14H10 and deuterated anthracene (C14D10) powders have been made up to a dose of 7 × 108 rad. Interpretation of the spectra is consistent with that resulting from the hyperfine interaction of three equivalent protons. Excessive breadth of the spectrum of the radical produced in C14D10 is attributed
G. A. Simpson +3 more
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Anthracene and Anthracene-Tetracene Crystals from Vapor
Molecular Crystals, 1968Abstract Molecular crystals in general are receiving increased attention and anthracene crystals in particular are in demand for use in various studies. Consequently, several techniques have been developed for growing anthracene crystals–most of which have involved growth from the melt.1–3 In those common method is to use a cooled collector plate.3,4 ...
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Gaschromatographic Determination of Anthracene and Hydrogenated Anthracene
Journal für Praktische Chemie, 1977P. Lobitz, W. Jabs, G. Schmidt
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Synthesis of Octaaryl Naphthalenes and Anthracenes with Different Substituents.
Angewandte Chemie, 2017Shin Suzuki +2 more
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