Results 171 to 180 of about 3,998 (209)
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Cyclobutanes in Catalysis

Angewandte Chemie International Edition, 2011
AbstractThe exploitation of ring strain as a driving force to facilitate chemical reactions is a well‐appreciated principle in organic chemistry. The most prominent and most frequently used compound classes in this respect are oxiranes and cyclopropanes.
Tobias, Seiser   +3 more
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Synthesis of Cyclobutane Nucleosides

Nucleosides, Nucleotides & Nucleic Acids, 2011
2-(6-Chloropurinyl)-3-benzoyloxymethylcyclobutanone can be prepared by reaction of 6-chloropurine with 3-benzoyloxymethyl-2-bromocyclobutanone. The N-alkylation gave both N-9 and N-7 regioisomers. Both regioisomers upon hydride reduction followed by aminolysis gave the corresponding adenine nucleoside analogues.
Abdelaziz, Ebead   +2 more
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Cyclobutane analogs of GABA

Neurochemical Research, 1980
Both cis- and trans-3-aminocyclobutane-1-carboxylic acid have been synthesized as conformationally restricted analogs of GABA. The cis isomer displayed weak to moderate GABA-like activity with respect to (1) inhibition of GABA uptake in rat brain minislices, (2) inhibition of sodium-independent binding of GABA to rat brain membranes, (3) activity as a ...
R D, Allan   +6 more
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Cyclobutanes from Combretum albopunctatum

Phytochemistry, 2004
A dichloromethane extract of the aerial parts of Combretum albopunctatum Suesseng afforded five phenolic compounds-three known flavonoids and two novel cyclobutane chalcone dimers. The chemical structures were determined by standard spectroscopic techniques and the structure and relative stereochemistry of one chalcone dimer, rel-(1 alpha,2 beta)-di-(2,
Katerere, D.R.   +4 more
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Infrared and Raman spectra of cyclobutane and cyclobutane-d8

Spectrochimica Acta Part A: Molecular Spectroscopy, 1972
Abstract New i.r. and Raman measurements are reported for cyclo butane and cyclo butane- d 8 . They include i.r. spectra on the gas at room temperature and on the solid at about 100°K. Raman spectra have been measured for the gas and liquid at room temperature and for the solid at 113°K. These data allow the assignments (for D 2d ) to be put on
Foil A. Miller   +3 more
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Cycloreversion of cyclobutanes

Theoretica Chimica Acta, 1980
Semiempirical MO calculations with the method SINDO1 were performed to study the potential energy surface of cyclobutane and several substituted cyclobutanes with substituents F, OCH3 and CN. The reaction pathway with the lowest activation energy leading to two ethylenic fragments is nonconcerted.
Karl Jug, Peter L. Müller
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Nonplanar cyclobutane—II

Tetrahedron, 1967
Abstract NMR spectra and basic equilibration of cis and trans methyl-3-isopropylcyclobutanecarboxylate are reported. Treatment of the nonplanar cyclobutane system by analogy with cyclohexane is potentially possible, but limited by (1) greater dependence of ring puckering on substituents; and (2) intervention of planar conformers.
I. Lillien, R.A. Doughty
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Bioactive cyclobutane-containing alkaloids

Journal of Natural Medicines, 2007
The present review describes research on novel natural cyclobutane-containing alkaloids and synthetic compounds isolated from terrestrial and marine species. More than 210 compounds have been confirmed to show antimicrobial, antibacterial, anticancer, and other activities.
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Conformations of cyclobutane

Tetrahedron, 1974
Abstract The literature concerning the structures of compounds containing saturated, 4-carbon rings is reviewed critically, and the variety of conformations (dihedral angles of 0° to 30° ± 6°) of the cyclobutane ring are tabulated and discussed.
F.Albert Cotton, Bertram A. Frenz
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Cyclobutan‐tetracarbonsäuren‐(1.2.3.4)

Chemische Berichte, 1960
AbstractDurch Ozonabbau von Truxillsäuren konnten 3 der 4 möglichen Cyclobutantetracarbonsäuren‐(1.2.3.4) hergestellt werden.
Rudolf Criegee, Hermann Höver
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