Results 121 to 130 of about 2,586 (168)
Some of the next articles are maybe not open access.

Oxidation of menthone oxothiolane

Chemistry of Natural Compounds, 2008
meta-Chloroperoxybenzoic acid (m-ClPBA) was shown to be an oxidant for two stereoisomers of menthone oxothiolane. The effect of steric factors on the ability to oxidize the sulfide group was found. Oxidation of (5S,6S,9R)-6-isopropyl-9-methyl-1-oxo-4-thiaspiro[4.5]-decane to the sulfone was prevented by the steric proximity of an isopropyl group to the
A. V. Timshina   +6 more
openaire   +1 more source

Menthone Semicarbazides and Thiosemicarbazides as Anticonvulsant Agents

Medicinal Chemistry, 2010
A series of novel (+/-) 3-menthone semi carbazides (1-7) and thiosemicarbazides synthesized using an appropriate synthetic route and characterized by thin layer chromatography and spectral analysis. The anticonvulsant activity of synthesized compounds was established after intraperitoneal administration in three seizure models in mice which include ...
Jainendra, Jain   +3 more
openaire   +2 more sources

Asymmetrical oxidation of menthone dithiolane

Russian Journal of Organic Chemistry, 2008
Asymmetrical oxidation was performed of menthone dithiolane obtained in 95–98% yield by condensation of menthone with 1,2-ethanedithiol in the presence of boron trifluoride etherate. 6-Isopropyl-9-methyl-1,4-dithiaspiro[4,5]decane-1,4-dioxide (yield 5–55%) and 6-isopropyl-9-methyl-1,4-dithiaspiro[4,5]-decane-1,1,4-trioxide (yield 65–70%) were ...
A. V. Timshina   +5 more
openaire   +1 more source

Chiral perrocenylalkylamines from (-)-menthone

Tetrahedron, 1986
Abstract Three enantiomerically pure ∝-ferrocenylalkylamines are directly obtained from (-)-menthone. The isomerizations of the ∝-ferrocenylalkyl carbocation intermediates are studied and exploited in stereoselective syntheses. These carbocations are the basis of the configurational assignment of the amines.
Franz Siglmüller   +2 more
openaire   +1 more source

Effect of cyclodextrin complexation on the reduction of menthone and isomenthone

Journal of Inclusion Phenomena, 1987
The β- and γ-cyclodextrin complexation of menthone and isomenthone was found to modify the ratio of epimeric menthol products formed upon a NaBH4/MeOH reduction of these ketones.
L. Szente, J. Szejtli, Le Tung Chau
openaire   +1 more source

Stereoselectivity of electroreduction of a menthone-isomenthone mixture

Russian Journal of Applied Chemistry, 2009
Electroreduction of an equilibrium menthone-isomenthone mixture at a controlled potential in a diaphragm cell on various cathodes was studied. The influence exerted by the nature of a solvent and of an electrode, electrode material, and various additives on the reduction stereoselectivity of ketones was examined.
N. D. Zubareva   +2 more
openaire   +1 more source

Home - About - Disclaimer - Privacy