Results 91 to 100 of about 135,807 (258)
A convenient preparation of novel benzophenone derivatives [PDF]
A simple and high yielding method for the synthesis of novel benzophenone derivatives has been developed starting from ethyl(4-aroylaroxy)acetates.
BELGUR S. SUDHA+2 more
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Mode of attack of hydriodic acid on unsaturated glyceryl ethers
The mode of action of hydriodic acid (HI) on a sample rich in selachyl alcohol [1-O-9(cis)-octadecenyl glycerol] has been studied. HI attacked the olefinic bonds as well as the ether bonds, with the formation of at least two diiodides as well as the ...
Donald J. Hanahan
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Studies on the biosynthesis of cholesterol. 3. Distribution of 14C in squalene biosynthesized from [Me-14C]-acetate [PDF]
J. W. Cornforth, G. Popják
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Liquid Organic Hydrogen Carriers: Hydrogenation Thermodynamics of Aromatic Esters
Aromatic esters such as phenyl acetates are of interest as promising liquid organic hydrogen carriers (LOHCs) due to the presence of double bonds.
Sergey P. Verevkin+3 more
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Oxidation of glucose, glycerol and acetate by Staphylococcus aureus [PDF]
Dorothy M. Powelson+2 more
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Dibenzo[a,g]quinolizin-8-ones: synthesis, estrogen receptor affinities, and cytostatic activity [PDF]
A number of acetoxy-substituted dibenzo[a,g]quinolizin-8-ones were synthesized by the reaction of 1-oxoisoquinolines with substituted homophthalic acid anhydride.
Angerer, S. von+4 more
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Effect of Reducing Atmosphere on the Magnetism of Zn1-xCoxO Nanoparticles
We report the crystal structure and magnetic properties of Zn1-xCoxO nanoparticles synthesized by heating metal acetates in organic solvent. The nanoparticles were crystallized in wurtzite ZnO structure after annealing in air and in a forming gas (Ar95 ...
A Fujimori+13 more
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STUDIES ON THE MECHANISM OF ACETATE OXIDATION BY BACTERIA [PDF]
Samuel J. Ajl
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Separation of sterol acetates by column and thin-layer argentation chromatography
Column and thin-layer chromatographic systems employing silver nitrate-impregnated adsorbents are described for the separation of sterol acetates which differ in the number of double bonds in the steroid nucleus or side chain.
Hugh E. Vroman, Charles F. Cohen
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