Results 121 to 130 of about 1,240 (135)
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Chemischer Informationsdienst, 1975
AbstractBei der Bromierung von Safrol (I) mit Brom in Chloroform entstehen die Bromierungsprodukte (II)‐(V), von denen die Verbindungen (III) und (V) durch Wagner‐ Meerwein‐Umlagerung gebildet werden.
T. IRINO, K. OTSUKI
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AbstractBei der Bromierung von Safrol (I) mit Brom in Chloroform entstehen die Bromierungsprodukte (II)‐(V), von denen die Verbindungen (III) und (V) durch Wagner‐ Meerwein‐Umlagerung gebildet werden.
T. IRINO, K. OTSUKI
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Reaction Kinetics, Mechanisms and Catalysis, 2011
Ultranox626 as a diphosphite ligand showed high selectivity and good yields when used with Rh(CO)2(acac) as a catalyst precursor in the hydroformylation of allylbenzene derivatives producing aldehydes, and also in the one-pot hydroformylation–acetalization forming acetals. These reactions proceed smoothly and effectively to produce the linear aldehydes
Mouheddin Alhaffar +3 more
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Ultranox626 as a diphosphite ligand showed high selectivity and good yields when used with Rh(CO)2(acac) as a catalyst precursor in the hydroformylation of allylbenzene derivatives producing aldehydes, and also in the one-pot hydroformylation–acetalization forming acetals. These reactions proceed smoothly and effectively to produce the linear aldehydes
Mouheddin Alhaffar +3 more
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Chemistry – A European Journal, 2014
AbstractWe describe a highly diastereoselective approach to anti‐homoallylic alcohols from allylbenzene derivatives and aldehydes. The strategy is based on a cross‐metathesis/isomerization/allylboration sequence catalyzed successively by ruthenium and iridium.
Hemelaere, Rémy +2 more
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AbstractWe describe a highly diastereoselective approach to anti‐homoallylic alcohols from allylbenzene derivatives and aldehydes. The strategy is based on a cross‐metathesis/isomerization/allylboration sequence catalyzed successively by ruthenium and iridium.
Hemelaere, Rémy +2 more
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Covalent binding to DNA in vitro of 2',3'-oxides derived from allylbenzene analogs.
Drug Metabolism and Disposition, 1996Epoxidation at the allylic side chain is a major metabolic pathway for allylbenzene and its naturally occurring analogs safrole, estragole, and eugenol. We demonstrate herein that the epoxide metabolites of allylbenzene, estragole, and safrole can form covalent adducts with DNA in vitro, binding primarily to guanine, but also to the other three DNA ...
G, Luo, T M, Guenthner
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Chemischer Informationsdienst, 1981
Abstract(IX), von denen das Methoxyindan (IX) auch aus der Verbindung (X) zugänglich ist.
S. JOLIDON, H.‐J. HANSEN
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Abstract(IX), von denen das Methoxyindan (IX) auch aus der Verbindung (X) zugänglich ist.
S. JOLIDON, H.‐J. HANSEN
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Chemischer Informationsdienst, 1980
AbstractPiperylen, Butadien und Cyclohexadien an schema skizziert.
S. JOLIDON, H.‐J. HANSEN
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AbstractPiperylen, Butadien und Cyclohexadien an schema skizziert.
S. JOLIDON, H.‐J. HANSEN
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Chemischer Informationsdienst, 1981
AbstractDie Be‐ Strahlung der (S)‐Amine (I) in Methanol liefert die Produkte (II), (III) und (IV).
B. SCHOLL, H.‐J. HANSEN
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AbstractDie Be‐ Strahlung der (S)‐Amine (I) in Methanol liefert die Produkte (II), (III) und (IV).
B. SCHOLL, H.‐J. HANSEN
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Biochimica et Biophysica Acta (BBA) - General Subjects, 1977
The acidic and neutral urinary metabolites of allylbenzene, propenylbenzene, 1'-hydroxyallylbenzene, and cynnamyl alcohol were identified and related through a common metabolic scheme. The rat metabolizes allylbenzene to 1'-hydroxyallylbenzene which can rearrange to yield cinnamyl alcohol whick is further metabolized.
J D, Peele, E O, Oswald
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The acidic and neutral urinary metabolites of allylbenzene, propenylbenzene, 1'-hydroxyallylbenzene, and cynnamyl alcohol were identified and related through a common metabolic scheme. The rat metabolizes allylbenzene to 1'-hydroxyallylbenzene which can rearrange to yield cinnamyl alcohol whick is further metabolized.
J D, Peele, E O, Oswald
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ChemInform, 1992
AbstractChemInform 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.
D. BROMM +3 more
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AbstractChemInform 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.
D. BROMM +3 more
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Macromolecular Chemistry and Physics, 2000
Functional poly(1,4-ketone)s were prepared by alternating copolymerization of carbon monoxide with substituted allylbenzenes, namely 2-allylphenol 1. 2-allyl-4-methylphenol 2. 2-allyl-6-methylphenol 3. 2-allylmethoxybenzene 4. 2-allylethoxybenzene 7.
Roland Wursche, Bernhard Rieger
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Functional poly(1,4-ketone)s were prepared by alternating copolymerization of carbon monoxide with substituted allylbenzenes, namely 2-allylphenol 1. 2-allyl-4-methylphenol 2. 2-allyl-6-methylphenol 3. 2-allylmethoxybenzene 4. 2-allylethoxybenzene 7.
Roland Wursche, Bernhard Rieger
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