Results 251 to 260 of about 19,882 (280)
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ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
E. E. Schultz+6 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
E. E. Schultz+6 more
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ChemInform Abstract: CYCLOPROPANATIONS WITH DIMETHYLCARBENE
Chemischer Informationsdienst, 1981AbstractDurch Addition von Dimethylcarben, intermediär gebildet aus 2,2‐Dibrompropan (II) und Butyllithium (III), an die Alkene (I) werden die Cyclopropane (IV) erhalten.
P. Fischer, G. Schaefer
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The Protonation of Gaseous Cyclopropane
Chemistry - A European Journal, 2001The protonation of cyclopropane by gaseous Brønsted acids of varying strength in radiolytic experiments at atmospheric pressure leads to two distinct C3H7- isomers that have been sampled by their reaction with benzene. The neutral end products, nC3H7-C6H5 and iC3H7-C6H5, arise from the electrophilic aromatic substitution reaction with the cC3H7+ and ...
CHIAVARINO, Barbara+3 more
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ChemInform Abstract: A Novel Cyclopropanation.
ChemInform, 1996AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
T. J. Connolly+6 more
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Stereoselective Cyclopropanation Reactions
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
André B. Charette+3 more
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Journal of the American Chemical Society, 1993
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Jason G. Hamilton, William E. Palke
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Jason G. Hamilton, William E. Palke
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Spectra and Structure of Crystalline Cyclopropane and Cyclopropane-D6
The Journal of Chemical Physics, 1969Infrared and Raman spectra of polycrystalline C3H6 and C3D6 were measured between 10 and 3500 cm−1 at 85°K. Infrared spectra of mixed C3H6 and C3D6 crystals were also obtained. From these measurements, an assignment of the origin of the multiplet splittings is proposed.
John B. Bates+2 more
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Transformation of thioacetals to cyclopropanes
Tetrahedron Letters, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Hirohisa Shimokawa+3 more
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Canadian Journal of Chemistry, 2001
Thermolysis of 2-cinnamyloxy-2-methoxy-5,5-dimethyl-Δ3-1,3,4-oxadiazoline (1a) and the analogous 2-benzyloxy-2-methoxy compound (1b) at 110°C, in benzene containing benzylidenemalononitrile, afforded products of apparent regiospecific addition of methoxycarbonyl and cinnamyl (or benzyl) radicals to the double bond.
Nadine Merkley+2 more
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Thermolysis of 2-cinnamyloxy-2-methoxy-5,5-dimethyl-Δ3-1,3,4-oxadiazoline (1a) and the analogous 2-benzyloxy-2-methoxy compound (1b) at 110°C, in benzene containing benzylidenemalononitrile, afforded products of apparent regiospecific addition of methoxycarbonyl and cinnamyl (or benzyl) radicals to the double bond.
Nadine Merkley+2 more
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1991
Publisher Summary This chapter describes the methods of construction of cyclopropane rings. This is followed by a discussion on the utility of cyclopropanes in organic synthesis with emphasis on the cleavage of the three-membered carbocycles by various reagents. The chapter also outlines several important earlier developments in this field.
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Publisher Summary This chapter describes the methods of construction of cyclopropane rings. This is followed by a discussion on the utility of cyclopropanes in organic synthesis with emphasis on the cleavage of the three-membered carbocycles by various reagents. The chapter also outlines several important earlier developments in this field.
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