Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Werner Löwe"'
Autor:
Werner Löwe, Anja Lüth
Publikováno v:
Journal of Heterocyclic Chemistry. 45:703-708
The epidermal growth factor (EGF) family of membrane receptors has been identified as a key element in the complex signaling network that is utilized by various classes of cell-surface receptors. A new synthetic pathway of 4-(indol-3-yl)quinazolines
Autor:
Werner Reutter, Frédéric Cantagrel, Michael Mickeleit, Stephan Laabs, Burkhard Kleuser, Werner Löwe, Annette Fischer, Martin Zimmermann-Kordmann, Dieter Dr. Müller, Kerstin Danker
Publikováno v:
ChemBioChem. 7:441-449
The search for specific anticancer drugs that do not interfere with DNA synthesis or influence the cytoskeleton has led to the development of modified phospholipids with antiproliferative properties. These compounds cause remodeling of the structure
Publikováno v:
Journal of Heterocyclic Chemistry. 38:365-370
Under basic conditions 2,6-bis(bromomethyl)-4-pyrone 8 reacts with tetraethylene glycol to yield the unexpected macrocycle 9, which is related to the antibiotic Kjellmanianone 10. We propose that this ring transformation proceeds via the cyclopropyl
Autor:
Werner Löwe, Thomas Braden
Publikováno v:
Archiv der Pharmazie. 324:949-951
Die bisher unbekannten 1,3,2-Benzodioxathiine 5, 6 werden aus den Enaminonen 1, 2 durch Reaktion mit Chlorsulfonsaure oder Oleum erhalten. Die Verbindungen 5, 6 lassen sich in die Oxime 7, 8, in die Oximester 11, 12, in die 2,4-Dinitrophenylhydrazone
Autor:
Norbert Matzanke, Holger Stark, Sylvie Perachon, Pierre Sokoloff, Werner Löwe, Jean-Charles Schwartz
Publikováno v:
European Journal of Medicinal Chemistry. 34:791-798
With a straightforward seven-step synthesis, racemic perhydro[1,4]benzoxazin-6-on was synthesized in overall good yields via regioselective epoxid ring-opening to the corresponding β-aminoalcohol. The oxazine derivative was the key intermediate for
Publikováno v:
Journal of Heterocyclic Chemistry. 34:1173-1178
We report here the syntheses and characterization of new crown-type compounds 8 and 9 incorporated with one and two 4-pyrone units. The reaction of compound 3 with 1,5-bis(2-hydroxyphenoxy)-3-oxapentane or catechol gave the desired molecules 8 and 9
Autor:
Norbert Matzanke, Werner Löwe
Publikováno v:
Journal of Heterocyclic Chemistry. 33:763-766
We examined the scope of the previously reported one-pot synthesis [1] of chromone-3-sulfonylureas. Different anilines and heterocyclic amines were thereby reacted with chlorosulfonyl isocyanate-derived chlorosulfonylureas. These were treated with di
Autor:
Werner Löwe, Norbert Matzanke
Publikováno v:
Journal of Heterocyclic Chemistry. 33:943-948
The synthesis of new flavone-3-sulfonylurea derivatives is hereby described. The influence of a phenyl group in the 2-position and an acetate group in the 8-position at the chromone nucleus on the activity was studied. Only weak cytostatic activity o
Publikováno v:
Journal of Heterocyclic Chemistry. 32:249-254
The new, fluorinated benzoxathiinopyrazole 4 and the hitherto unknown fluorinated benzoxathiinodihydropyridine 5 can be produced by reacting the title compound 1 with cyanoacetic hydrazide (3) in the presence of sodium acetate. The structures of the
Autor:
Werner Löwe, Annette Kietzmann
Publikováno v:
Archiv der Pharmazie. 328:11-15
Ausgehend vom tosylierten Enaminon 5 lassen sich mit Essigsaure, Sulfurylchlorid und Thionylchlorid die neuen Chinolon-Derivate 3, 8, 9 und 10 herstellen. Das schwefelverbruckte Bischinolon 8 gibt bei der Alkylierung die N-Alkylprodukte 11 und 12. Di