Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Peer Fehling"'
Publikováno v:
European Journal of Lipid Science and Technology. 113:380-386
For the reduction of 3-monochloro-1,2-propanediol fatty acid esters (3-MCPD esters) and related compounds in edible fats and oils three different strategies are conceivable: removal of critical reactants from the raw material, changing of the refinin
Autor:
Patrick Benecke, Andrea Schwaf, Peer Fehling, Anne Sigrid Freudenstein, Frank Pudel, Bertrand Matthäus
Publikováno v:
European Journal of Lipid Science and Technology. 113:368-373
A framework of collaborating research facilities in Germany investigates the reasons and conditions for the formation of 3-monochloro-1,2-propanediol esters (3-MCPD-E) and of glycidyl esters (GE) during edible oil refining. The aim is the derivation
Publikováno v:
Composites Part B: Engineering. 39:362-373
Starting out from damage-tolerant oxidic composites with carbon (C)-coated fibers, the main part of our investigations was concentrated on Nextel 440-fibers/glass matrix composites. The matrix glasses were chosen in consideration of suitable thermal
Publikováno v:
Journal of Heterocyclic Chemistry. 38:205-211
The synthesis of pyrido[2,1-c]-1,2,4-triazines 6, pyrido[1,2-b]-1,2,4-triazines 7 and pyrido[1,2-b]pyri-dazines 8 respectively by cycloacylation of derivatives of pyridine with imidoylchlorides of type 2 is described. The heterocycles of type 6 as we
Autor:
Jörg Brandenburg, Rainer Beckert, Thomas Billert, Manfred Döring, Peer Fehling, Peter Langer, Helmar Görls
Publikováno v:
Journal of Heterocyclic Chemistry. 36:627-633
The reaction of pyrido[1,2-a]pyrazines 1 with nitroso compounds 2 provides pyridyl substituted 1,2,4-triazinones 4 via a domino reaction which involves a cycloaddition and a ring transformation reaction. The intermediate and regioselective formed oxa
Publikováno v:
Tetrahedron. 53:5455-5462
An expedient one-pot synthesis via a novel cycloaddition/ring transformation sequence allows the introduction of two arylamino groups and a pyridine substructure on azaquinones. Using 1,4-benzoquinone a twofold regioselective reaction yields the deep
Publikováno v:
Journal f�r Praktische Chemie/Chemiker-Zeitung. 338:430-435
Bicyclic Oxalic Amidines as Building Blocks for Highly Substituted 2,2′-Bipyridines and Benzene Derivatives The bis-imidoylchlorides 1 derived from oxalic acid exhibit a high regio- and chemoselectivity. As in the case of 2-picolylamine 2 the acyla
Publikováno v:
Chemische Berichte. 128:405-412
Ion Pairing and Cyclization on Coordinatively Bound Oxalamidines The tetraphenyloxalamidine ligand of complex 8a reacts easily in the presence of bases with elementorganic dichlorides (R2MCl2) to form coordinated metalacycles. The cyclization with ph
Publikováno v:
Journal f�r Praktische Chemie/Chemiker-Zeitung. 337:143-152
On the Aminolysis of Bis-Imidoylchlorides of Oxalic Acid. Part I. Reaction with Aromatic and Aliphatic Amines The reaction between bis-imidoylchlorides 2 derived from oxalic acid and several aromatic and aliphatic amines was investigated. While prima
Publikováno v:
ChemInform. 26