Ralph Kluge - Academia.edu (original) (raw)
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Papers by Ralph Kluge
Synlett, 1993
ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform 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.
J Org Chem, 1997
The reaction of ketones (acetone, 1,1,1-trifluoropropan-2-one) with the oxidation system (arenesu... more The reaction of ketones (acetone, 1,1,1-trifluoropropan-2-one) with the oxidation system (arenesulfonyl)imidazole (2)/H(2)O(2)/NaOH permits the in situ generation of the corresponding dimethyl- and methyl(trifluoromethyl)dioxirane in various solvents. This has been established by the chemoselective oxidation of azomethines 6, the diastereoselective oxidation of cholesterol (12), and (18)O-labeling experiments. Because only 5 equiv of ketone are used, the dioxirane oxidation pathway appears to be virtually exclusive one in this system. One example for the nonaqueous in situ generation of dimethyldioxirane (1a) is given.
ChemInform, 1992
ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6... more ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6-tri-tert-butyl-phenoxy radical (2). It was shown that the oxidation did not lead to the azo compounds 5a, b. but rather to radical combination products 6a. b of 2 via the intermediate hydrazyls 4a. b, The decomposition of adducts 6a, b was found to be similar to the reaction of radical combination products of aryl hydrazyls and CH-acidic compounds. The main reactions consisted of cleavage to starting radicals or elimination of isobutene forming the respective phenolic compounds 13a-c.
Journal f�r Praktische Chemie, 1988
Journal f�r Praktische Chemie/Chemiker-Zeitung, 1996
Zeitschrift für Chemie, 1989
ChemInform, 1995
ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6... more ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6-tri-tert-butyl-phenoxy radical (2). It was shown that the oxidation did not lead to the azo compounds 5a, b. but rather to radical combination products 6a. b of 2 via the intermediate hydrazyls 4a. b, The decomposition of adducts 6a, b was found to be similar to the reaction of radical combination products of aryl hydrazyls and CH-acidic compounds. The main reactions consisted of cleavage to starting radicals or elimination of isobutene forming the respective phenolic compounds 13a-c.
ChemInform, 1996
ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform 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.
ChemInform
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more ChemInform 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.
Zeitschrift für Chemie, 1988
Zeitschrift für Chemie, 1987
Tetrahedron: Asymmetry, 1998
Tetrahedron: Asymmetry, 1997
Synlett, 1993
ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform 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.
J Org Chem, 1997
The reaction of ketones (acetone, 1,1,1-trifluoropropan-2-one) with the oxidation system (arenesu... more The reaction of ketones (acetone, 1,1,1-trifluoropropan-2-one) with the oxidation system (arenesulfonyl)imidazole (2)/H(2)O(2)/NaOH permits the in situ generation of the corresponding dimethyl- and methyl(trifluoromethyl)dioxirane in various solvents. This has been established by the chemoselective oxidation of azomethines 6, the diastereoselective oxidation of cholesterol (12), and (18)O-labeling experiments. Because only 5 equiv of ketone are used, the dioxirane oxidation pathway appears to be virtually exclusive one in this system. One example for the nonaqueous in situ generation of dimethyldioxirane (1a) is given.
ChemInform, 1992
ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6... more ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6-tri-tert-butyl-phenoxy radical (2). It was shown that the oxidation did not lead to the azo compounds 5a, b. but rather to radical combination products 6a. b of 2 via the intermediate hydrazyls 4a. b, The decomposition of adducts 6a, b was found to be similar to the reaction of radical combination products of aryl hydrazyls and CH-acidic compounds. The main reactions consisted of cleavage to starting radicals or elimination of isobutene forming the respective phenolic compounds 13a-c.
Journal f�r Praktische Chemie, 1988
Journal f�r Praktische Chemie/Chemiker-Zeitung, 1996
Zeitschrift für Chemie, 1989
ChemInform, 1995
ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6... more ABSTRACT N-Heterocyclic compounds 1a, b containing the hydrazo StruCture were oxidized with 2.4,6-tri-tert-butyl-phenoxy radical (2). It was shown that the oxidation did not lead to the azo compounds 5a, b. but rather to radical combination products 6a. b of 2 via the intermediate hydrazyls 4a. b, The decomposition of adducts 6a, b was found to be similar to the reaction of radical combination products of aryl hydrazyls and CH-acidic compounds. The main reactions consisted of cleavage to starting radicals or elimination of isobutene forming the respective phenolic compounds 13a-c.
ChemInform, 1996
ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform 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.
ChemInform
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more ChemInform 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.
Zeitschrift für Chemie, 1988
Zeitschrift für Chemie, 1987
Tetrahedron: Asymmetry, 1998
Tetrahedron: Asymmetry, 1997
Cheminform, 2010
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more ChemInform 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.