Results 121 to 130 of about 652 (178)
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Lignans, γ-lactones and propiophenones of Virola surinamensis

Phytochemistry, 1996
Abstract The leaves and seeds of Virola surinamensis contain 17 lignans; fragansins A2 and D2, galbacin, galbelgin, 5-methoxygalbelgin, grandisin, verrucosin, aristolignan, austrobailignan, calopeptin, veraguensin, 5-methoxyveraguensin, nectandrin B, galbulin and galcatin; three propiophenone derivatives; two γ-lactones; juruenolide C and ...
Norberto Peporine Lopès   +2 more
exaly   +2 more sources

NIS‐Catalyzed Reactions: Amidation of Acetophenones and Oxidative Amination of Propiophenones

Chemistry - A European Journal, 2012
Single-step amination: the N-iodosuccinimide (NIS)-catalyzed amidation of acetophenone derivatives by using tert-butylhydroperoxide (TBHP) as an oxidant is presented. A variety of acetyl derivatives of heterocyclic compounds were easily converted to their corresponding ketoamides under these conditions.
Manjunath LaMani   +1 more
exaly   +3 more sources

Excess molar volumes of (propiophenone + toluene) and estimated density of liquid propiophenone below its melting temperature

The Journal of Chemical Thermodynamics, 2006
Abstract The densities of liquid propiophenone and toluene, and of their mixtures were measured at six temperatures between 283.15 K, and 328.15 K by means of a vibrating-tube densimeter. The excess molar volumes V m E calculated from the density data show that the deviations from ideal behaviour in the systems studied (all being ...
L. Morávková, J. Linek
openaire   +1 more source

2'-(Diphenylphosphino)propiophenone, a Functionalized Tertiary Phosphine

Acta Crystallographica Section C Crystal Structure Communications, 1995
The structure of the title compound, Ph 2 P(o-C 6 H 4 -CO-C 2 H 5 ), shows significant distortions from tetrahe dral geometry around the P atom; the C21-P1-C31 angle between the two unsubstituted rings [99.69 (9) o ] is smaller than the other two C-P-C angles [104.37 (9) and 102.24(9) o ]. The P-C distances are 1.828(2), 1.846 (2) and 1.851 (2) A.
B. T. Rasley, M. Rapta, R. J. Kulawiec
openaire   +1 more source

The effects of cofactor and species differences on the in vitro metabolism of propiophenone and phenylacetone

Canadian Journal of Physiology and Pharmacology, 1981
In vitro metabolism of the aromatic ketone propiophenone and its nonaromatic isomer phenylacetone was studied using fortified 12 000 × g supernatants of liver homogenates from rat and rabbit. Reduction to the corresponding alcohols was the major metabolic route observed, although aliphatic C-hydroxylation and alcohol dehydrogenation also occurred ...
R T, Coutts, D B, Prelusky, G R, Jones
openaire   +2 more sources

Kinetic Study on Hydrogenation of Propiophenone Catalyzed by Chitosan-Palladium

2010
Chitosan-palladium complex (SiO2-CS-Pd) is prepared and used as catalyst to catalyze the hydrogenation of propiophenone. The reaction is taken placed at normal temperature and 1 atm H2. The solvent is alcohol. GC is used to test the reaction course. The reaction is found to be pseudo-zero order with respect topropiophenone.
Hong-Lei Wang   +4 more
openaire   +1 more source

Electron transfer processes in the photochemistry of .beta.-(dimethylamino)propiophenone

Journal of the American Chemical Society, 1979
The photochemistry of ..beta..-(dimethylamino)propiophenone has been examined in aqueous solvents using laser flash photolysis technique. The triplet state decays via charge-transfer interactions which lead to intramolecular electron transfer and a product which is best described as a biradical zwitterion; the yield of biradical generation is 0.18 in ...
M. V. Encinas, J. C. Scaiano
openaire   +1 more source

ChemInform Abstract: Condensation of Some Propiophenones with Dimethyl Homophthalate.

Chemischer Informationsdienst, 1985
AbstractDie Stobbe‐Kondensation der Propiophenone (I) mit dem Homophthalsäureester (II) liefert die Halbester (III) als trennbares E,Z‐Gemisch.
M. F. EL‐NEWAIHY   +4 more
openaire   +1 more source

Some novel cyclizations of propiophenones with chlorosulfonic acid

Journal of Heterocyclic Chemistry, 1966
AbstractThe reaction of chlorosulfonie acid with propiophenones was found to give the 3‐chloro‐2‐methylbenzothiophene‐1, 1‐dioxides (I) and (VIII); reaction of Mannich bases of aceto‐phenone, with chlorosulfonie acid, gave the corresponding 3‐chloro‐2‐substituted amino‐methylbenzothiophene‐1,1‐dioxides (IX) and (X).
openaire   +1 more source

Reductive dimerization of propiophenone

Pharmaceutical Chemistry Journal, 1989
V. A. Zolotareva   +3 more
openaire   +1 more source

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