Results 161 to 170 of about 1,748 (205)
Some of the next articles are maybe not open access.

Adsorption geometry and core excitation spectra of three phenylpropene isomers on Cu(111).

The Journal of Chemical Physics, 2006
Theoretical C 1s near edge x-ray absorption fine structure (NEXAFS) spectra for the C9H10 isomers trans-methylstyrene, α-methylstyrene, and allylbenzene in gas phase and adsorbed at Cu(111) surfaces have been obtained from density functional theory calculations where adsorbate geometries were determined by corresponding total energy optimizations.
C. Kolczewski   +7 more
semanticscholar   +4 more sources

Cobalt, nickel, and copper coordination compounds with 3-phenylpropenal benzoylhydrazone

Russian Journal of General Chemistry, 2006
3-Phenylpropenal benzoylhydrazone (HL) reacts with cobalt, nickel, and copper chlorides, nitrates, and acetates to give coordination compounds MX2 · nH2O [M = Co, Ni, Cu; X = Cl, NO3, HL = C6H5CH=CHCH=NNHC(O)C6H5; n = 0, 2] and ML2 · nH2O (M = Co, Ni, Cu; n = 1–3).
N. M. Samus’   +2 more
  +4 more sources

Bioherbicidal activity of terpenes and phenylpropenes against Echinochloa crus-galli

Journal of Environmental Science and Health, Part B, 2019
This study was undertaken to evaluate the herbicidal activity of twelve natural compounds belonging to monoterpenes, phenylpropenes, and sesquiterpenes against Echinochloa crus-galli under laboratory and glasshouse conditions. Experiments were conducted to determine the impact of different concentrations (0.5, 1, 2, 4 and 8 mM) of these compounds on ...
Mona M. G. Saad   +2 more
openaire   +2 more sources

Enantioselectivity in the Rabbit Liver Microsomal Biotransformation of Styrene and Phenylpropenes

Biocatalysis, 1994
The rabbit liver microsomal P-450 catalyzed oxidation of styrene (1a) and isomeric phenylpropenes, trans-1-phenylpropene (1b), cis-1-phenylpropene (1c) and 3-phenylpropene (1d), was investigated and the enantioselectivity of the epoxidation of the olefinic double bond was determined by checking the enantiomeric excesses of the corresponding first ...
BELLUCCI G   +3 more
openaire   +2 more sources

1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-3-phenylpropene from Lindera lucida

Phytochemistry, 1998
Abstract A new diarylpropene, 1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-3-phenylpropene, has been isolated from twigs of Lindera lucida. Its structure was determined by spectral analysis and chemical correlation.
Leong, Y.-W.   +3 more
openaire   +1 more source

ChemInform Abstract: Oxidative Photoaddition of N‐Nitrosodimethylamine to 1‐Phenylpropenes.

ChemInform, 1987
AbstractIn the presence of HCl and under oxygen purging, the nitrosamine (V) photolytically adds to the arylpropenes (Ia), (Ic) to give threo‐ and erythro‐α‐amino nitrates (III) or (VIII) as the primary products which are reduced to yield the α‐amino alcohols (IV) or (IX), respectively.
Y. L. CHOW, Z.‐Z. WU
openaire   +1 more source

Oxidative photoaddition of N‐nitrosodimethylamine to 1‐phenylpropenes

Recueil des Travaux Chimiques des Pays-Bas, 1986
AbstractIn the presence of hydrochloric acid and under oxygen purging, N‐nitrosodimethylamine photolytically adds to 1‐arylpropenes regiospecifically to give erythro‐ and threo‐α‐amino nitrates as the primary products which can then be reduced, using lithium aluminium hydride, to give α‐amino alcohols or can undergo substitution reactions under ...
Yuan L. Chow, Zheng‐Zhi Wu
openaire   +1 more source

Alkylation of p-cresol with 3-phenylpropen-1-ol-3

Bulletin of the Academy of Sciences, USSR Division of Chemical Science, 1964
1. The alkenylation of p-cresol with phenacyl alcohol in the presence of zinc chloride on aluminum oxide goes in the direction of the formation of 1-phenyl-3-(3-methyl-6-hydroxphenyl)propene-1 in 80% of theoretical yield. 2. The alkenylation of p-cresol with phenacyl alcohol proceeds with a larger yield than the allylation of p-cresol ...
E. A. Viktorova   +2 more
openaire   +1 more source

Home - About - Disclaimer - Privacy