Results 151 to 160 of about 1,748 (205)
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Singlet-state cis-trans photoisomerization of 1-phenylpropene
Journal of the American Chemical Society, 1993F. Lewis, D. Bassani
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2,4-Dinitrobenzenesulphenylnitrene: addition to (Z)- and (E)-1-phenylpropene
Journal of the Chemical Society, Perkin Transactions 1, 1982Oxidation of 2,4-dinitrobenzenesulphenamide (1) with lead tetra-acetate in the presence of (Z)-1-phenylpropene gives a ca. 3:1 mixture of cis- and trans-aziridines (3) and (4), respectively. This ratio is unchanged over a tenfold decrease in concentration of (Z)-1-phenylpropene.
R. S. Atkinson, B. Judkins, N. Khan
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ChemInform Abstract: Special Features of 2‐Phenylpropene Arenesulfonation.
ChemInform, 2000AbstractChemInform 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.
E. E. Bilaya +2 more
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Synthesis of N-(1-carboxy-3-phenylpropen-2yl)alanylproline
Chemistry of Heterocyclic Compounds, 1996A method has been developed for the synthesis of N-(1-carboxy-3-phenylpropen-2-yl)atanylproline by reductive alkylation of alanylproline by the sodium salt of 2-oxo-4-phenylbutenoic acid, using sodium cyanoborohydride and sodium borchydride as reducing agents. The products were separated chromatographically. Under the conditions of the reaction, sodium
V. A. Slavinskaya +6 more
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Enantioselective carbonylation reactions of para‐substituted 2‐phenylpropenes
Chirality, 1991AbstractThe enantioselective hydroformylation catalyzed by [(R,R)‐Diop]Pt(SnCl3)Cl7 and the enantioselective hydroisopropoxycarbonylation catalyzed by [(R,R)‐Diop]PdCl28 or by [(R,R)‐Diop‐dbp]PdCl29 of some para‐substituted 2‐phenylpropenes (para substituents = NO2, H, CH3O, Cl, CF3) was investigated in order to recognize possible electronic influences
Giambattista Consiglio, Lucia Roncetti
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Preparation and chemistry of some 1-Iodo-1-phenylpropenes
Australian Journal of Chemistry, 1971The oxidation of eight aryl alkyl hydrazones with iodine in the presence of triethylamine gave mixtures of 1-iodo-1-arylpropenes and ketones in yields of 36-73% and 19-43% respectively. Further evidence is presented in favour of an iodocarbonium ion intermediate for this reaction.
JR Campbell, A Pross, S Sternhell
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Phenylpropenes: Occurrence, Distribution, and Biosynthesis in Fruit
Journal of Agricultural and Food Chemistry, 2016Phenylpropenes such as eugenol, chavicol, estragole, and anethole contribute to the flavor and aroma of a number of important herbs and spices. They have been shown to function as floral attractants for pollinators and to have antifungal and antimicrobial activities.
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THE METHOXYMERCURATION OF 2-METHYL-1-PHENYLPROPENE-1
Canadian Journal of Chemistry, 1952The addition of the elements of methoxymercuric acetate to 2-methyl-1-phenylpropene-1 occurs to give 2-methyl-2-methoxy-1-phenylpropylmercuric acetate. This structure could not be demonstrated by replacement of chloromercuri by halogeno because 2-methyl-1,2-dimethoxy-1-phenylpropane and 2-methyl-2-phenylpropanal or 3-phenylbutanone-2 were obtained ...
L. Berman +3 more
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Hydrogen-atom attack on 1-phenylpropene at high temperatures
Symposium (International) on Combustion, 1994The reactions of hydrogen atom with 1-phenylpropene (IPP) have been studied in single-pulse shocktubeexperiments. Contribution from a large number of the possible reactive channels has been observed. The prime channels are the displacement of the methyl group resulting from addition to the olefinic structure and abstraction of a hydrogen from the ...
Wing Tsang, James A. Walker
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The monolignol pathway contributes to the biosynthesis of volatile phenylpropenes in flowers
New Phytologist, 2014Summary Volatile phenylpropenes play important roles in the mediation of interactions between plants and their biotic environments. Their biosynthesis involves the elimination of the oxygen functionality at the side‐chain of monolignols and competes with lignin formation for monolignol utilization.
Joëlle K, Muhlemann +3 more
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