Results 241 to 250 of about 86,821 (289)
Some of the next articles are maybe not open access.
Tetrahedron Letters, 2008
Acid promoted cyclization of the geranylamine N-oxide (E)-4 followed by base-catalyzed intramolecular aldol condensation afforded 1-acetyl-4,4-dimethyl-1-cyclohexene (7) in one-pot operation. Reduction of 7, which possess strong fruity odor, followed by lipase-catalyzed kinetic resolution furnished the acetate (R)-26 (>49.9% yield, >99% ee) and the ...
Kunihiko Takabe +3 more
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Acid promoted cyclization of the geranylamine N-oxide (E)-4 followed by base-catalyzed intramolecular aldol condensation afforded 1-acetyl-4,4-dimethyl-1-cyclohexene (7) in one-pot operation. Reduction of 7, which possess strong fruity odor, followed by lipase-catalyzed kinetic resolution furnished the acetate (R)-26 (>49.9% yield, >99% ee) and the ...
Kunihiko Takabe +3 more
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Chemischer Informationsdienst, 1980
AbstractDie cyclischen Acetylene (Ia) und (Ib) addieren elementaren Schwefel zu den Dithieten (IIa) und (IIb), mit Pyridin‐N‐oxid (III) und (Ia) IÖO wird das Spiroazepin (IV) erhalten, das thermisch in das Pyridylthiepinon (V) umgelagert werden kann.
A. KREBS +4 more
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AbstractDie cyclischen Acetylene (Ia) und (Ib) addieren elementaren Schwefel zu den Dithieten (IIa) und (IIb), mit Pyridin‐N‐oxid (III) und (Ia) IÖO wird das Spiroazepin (IV) erhalten, das thermisch in das Pyridylthiepinon (V) umgelagert werden kann.
A. KREBS +4 more
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ChemInform, 2000
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.
S. Raja Ram +2 more
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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.
S. Raja Ram +2 more
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Tetrahedron, 1982
Abstract 1,2-Oxazine N-oxides derived from aminocyclohexenes open into the corresponding nitroalkylated trisubstituted enamines, whereas those derived from aminocyclopentenes give stable tetrasubstituted enamines. Both open-chain systems are easily hydrolyzed to the corresponding γ-nitrocycloalkanones.
DANEO S. +3 more
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Abstract 1,2-Oxazine N-oxides derived from aminocyclohexenes open into the corresponding nitroalkylated trisubstituted enamines, whereas those derived from aminocyclopentenes give stable tetrasubstituted enamines. Both open-chain systems are easily hydrolyzed to the corresponding γ-nitrocycloalkanones.
DANEO S. +3 more
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ChemInform, 2010
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.
Julie Schleiss +2 more
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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.
Julie Schleiss +2 more
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Chemistry of Heterocyclic Compounds, 1988
4H-Imidazole 1,3-dioxides and 4H-imidazole 3-oxides were obtained by oxidation of 1-hydroxy-3-imidazoline 3-oxides and 1-hydroxy-3-imidazolines with lead and manganese dioxides or the stable nitroxyl radical, while 4H-imidazole 1-oxides were obtained by thermal decomposition of 1-acetoxy-3-imidazoline 3-oxides.
I. A. Grigor'ev +2 more
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4H-Imidazole 1,3-dioxides and 4H-imidazole 3-oxides were obtained by oxidation of 1-hydroxy-3-imidazoline 3-oxides and 1-hydroxy-3-imidazolines with lead and manganese dioxides or the stable nitroxyl radical, while 4H-imidazole 1-oxides were obtained by thermal decomposition of 1-acetoxy-3-imidazoline 3-oxides.
I. A. Grigor'ev +2 more
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Electrochimica Acta, 1987
Abstract The cathodic reductions of two series of substituted quinoxaline di- N -oxides and quinoxalines in acetonitrile were measured in the potential range of 0 to −2.0 V and 0 to −2.3 V vs sce , respectively. Two irreversible reductions were observed in the first series, and one reversible reduction for the second.
K.R. Barqawi, M.A. Atfah
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Abstract The cathodic reductions of two series of substituted quinoxaline di- N -oxides and quinoxalines in acetonitrile were measured in the potential range of 0 to −2.0 V and 0 to −2.3 V vs sce , respectively. Two irreversible reductions were observed in the first series, and one reversible reduction for the second.
K.R. Barqawi, M.A. Atfah
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ChemInform, 2000
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.
K. Purushothama Chary +2 more
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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.
K. Purushothama Chary +2 more
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ChemInform, 1989
AbstractOxidation of the 1‐hydroxy‐3‐imidazoline 3‐oxides (I) or the 1‐hydroxy‐3‐imidazolines (IIIa) and (IIIc) gives the dioxides (II) or the 4H‐imidazole 3‐monoxides (IVa) and (IVc).
I. A. GRIGOR'EV +2 more
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AbstractOxidation of the 1‐hydroxy‐3‐imidazoline 3‐oxides (I) or the 1‐hydroxy‐3‐imidazolines (IIIa) and (IIIc) gives the dioxides (II) or the 4H‐imidazole 3‐monoxides (IVa) and (IVc).
I. A. GRIGOR'EV +2 more
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Chemischer Informationsdienst, 1984
Abstract2‐Chlorimidazolin ( l) reagiert mit Chinolin‐ N‐oxiden (II) über die Zwischenstufe cyclischer Addukte zu 2‐lmidazolidinon‐Derivaten (III) und (IV).
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Abstract2‐Chlorimidazolin ( l) reagiert mit Chinolin‐ N‐oxiden (II) über die Zwischenstufe cyclischer Addukte zu 2‐lmidazolidinon‐Derivaten (III) und (IV).
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