Oxidation of Cyclohexane to Cyclohexanol/Cyclohexanone Using Sol-Gel-Encapsulated Unspecific Peroxygenase from Agrocybe aegerita. [PDF]
Wu Y, Hollmann F, Musa MM.
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Enantioselective Synthesis of Spirolactones and Spirolactams Under Low Catalyst Loadings. [PDF]
Saito T, Navarro A, Davies HML.
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Advances in α-Arylation of Carbonyl Compounds: Diaryliodonium Salts as Arylating Agents. [PDF]
Chen XW +5 more
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Synthesis and investigation of thieno[2,3-<i>b</i>]pyridines that restore activity of topotecan. [PDF]
Paulin EK +10 more
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2- (β-Cyanoethyl) cyclohexanone
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Revolutionizing organic synthesis through green chemistry: metal-free, bio-based, and microwave-assisted methods. [PDF]
Banerjee S +4 more
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Toxicological aspects of cyclohexanone
Toxicology and Applied Pharmacology, 1979Abstract A toxicity evaluation of cyclohexanone was conducted using oral, intraperitoneal, dermal, intradermal, ophthalmic, and/or inhalation exposure to various species of animals. Cyclohexanone induced diverse reactions by virtue of a general vascular or tissue reaction and CNS depression. The ip LD50 for mice, rats, guinea pigs, and rabbits ranged
P K, Gupta +3 more
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Oxovanadium(IV) complexes of cyclohexanone semicarbazone and cyclohexanone thiosemicarbazone
Transition Metal Chemistry, 1981Oxovanadium(IV) complexes, VOL2X2 (X = Cl, Br and 0.5 SO4), have been synthesised and characterised by elemental analysis, room temperature magnetic moment, electronic, i.r. and electron spin resonance studies. The complexes are hexacoordinate and have a distorted octahedral structure.
Sulekh Chandra, Krishna B. Pandeya
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Some chromium(III) complexes of cyclohexanone semicarbazone and cyclohexanone thiosemicarbazone
Journal of Inorganic and Nuclear Chemistry, 1980Chromium(III) complexes of cyclohexanone semicarbazone and cyclohexanone thiosemicarbazone have been prepared and characterized. Complexes of general composition Cr(ligand)2X3 are obtained (X = Cl or NO3). Magnetic moments, electronic spectra and ESR spectra of the complexes are discussed.
Sulekh Chandra, K.B. Pandeya, R.P. Singh
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In the presence of a small amount of sodium methylate, cyclohexanone and benzil form an addition product, which is a "semicyclic" 1:4-diketone. No derivatives of a bicyclic cyclo-heptane were found. Its most conspicuous chemical property is its sensitivity to mineral acids; among the reaction products is found a diphenyltetrahydrocumarone.
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