Results 241 to 250 of about 14,027,089 (269)
Some of the next articles are maybe not open access.

One‐Pot Synthesis of Substituted Indole N‐Oxides: TiCl4‐Mediated Baylis—Hillman Reaction of α‐Oxo Cyclic Ketene‐S,S‐acetal with o‐Nitrobenzaldehydes and Subsequent Intramolecular Cyclization.

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Wei Pan   +3 more
openaire   +1 more source

Enantioselective Addition of Cyclic Enol Silyl Ethers to 2‐Alkenoyl‐Pyridine‐N‐Oxides Catalysed by CuII–Bis(oxazoline) Complexes

Chemistry – A European Journal, 2012
AbstractAsymmetric reactions involving (E)‐3‐aryl‐1‐(pyridin‐2‐yl‐N‐oxide)prop‐2‐en‐1‐ones and cyclic enol silyl ethers show good yields and excellent enantioselectivities (up to 99.9 % ee) when catalysed by bis(oxazoline)–CuII complexes. Different reaction pathways can be followed by different enol silyl ethers: with 2‐(trimethylsilyloxy)furan, a ...
LIVIERI, ALESSANDRO   +3 more
openaire   +3 more sources

Cyclic Nitrone Free Radical Traps:  Isolation, Identification, and Synthesis of 3,3-Dimethyl-3,4-dihydroisoquinolin-4-ol N-Oxide, a Metabolite with Reduced Side Effects

Journal of Medicinal Chemistry, 1996
A C-4 hydroxylated metabolite (2, 3,3-dimethyl-3,4-dihydroisoquinolin-4-ol N-oxide) of the previously described cyclic nitrone free radical trap 1 (3,3-dimethyl-3,4-dihydroisoquinoline N-oxide, a cyclic analog of phenyl-tert-butylnitrone (PBN)) was isolated, identified, and synthesized.
C E, Thomas   +13 more
openaire   +2 more sources

Cyclic Conversion of the Novel Src Kinase Inhibitor [7-(2,6-Dichloro-phenyl)-5-methyl-benzo[1,2,4]triazin-3-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine (TG100435) and Its N-Oxide Metabolite by Flavin-Containing Monoxygenases and Cytochrome P450 Reductase

Drug Metabolism and Disposition, 2007
[7-(2,6-Dichloro-phenyl)-5-methyl-benzo[1,2,4]triazin-3-yl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine (TG100435) is a novel multi-targeted Src family kinase inhibitor with demonstrated anticancer activity in preclinical species. Potent kinase inhibition is associated with TG100435 and its major N-oxide metabolite [7-(2,6-dichlorophenyl)-5-methyl ...
Ahmed, Kousba   +3 more
openaire   +2 more sources

Model iron-catalyzed biomimetic cyclization of a cyclic tryptamine N-oxide

The Journal of Organic Chemistry, 1972
C A, Scherer   +3 more
openaire   +2 more sources

Strained Cyclic Acetylenes, VII. Addition of Sulfur and Pyridine-N-oxide to Seven Membered Cycloalkynes

HETEROCYCLES, 1979
Adolf Krebs   +4 more
openaire   +1 more source

Analogs of Aspergillic Acid. IV. Substituted 2-Bromopyridine-N-oxides and Their Conversion to Cyclic Thiohydroxamic Acids1

Journal of the American Chemical Society, 1950
Elliott Shaw   +3 more
openaire   +1 more source

Home - About - Disclaimer - Privacy