Results 141 to 150 of about 10,186 (207)
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Inverse-Electron-Demand Diels-Alder Reactions for the Synthesis of Pyridazines on DNA.
Organic Letters, 2018The synthesis of pyridazines on DNA has been developed on the basis of inverse-electron-demand Diels-Alder (IEDDA) reactions of 1,2,4,5-tetrazines. The broad substrate scope is explored.
Hailong Li +7 more
semanticscholar +1 more source
Pyridazines. III. The synthesis of substituted pyridazines
Journal of Heterocyclic Chemistry, 1965AbstractA series of pyridazines and pyridazones have been prepared substituted with alkyl, alkoxyl, halogen, mercapto, substituted mercapto, phenyl, morpholino, piperidino, styryl, substituted styryl and pyridylethenyl groups as potential antitumor agents. The compounds possessing antitumor or tissue culture activity are recorded in Table VI.
Raymond N. Castle, Kenji Kaji
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Journal of Organic Chemistry, 2019
A divergent synthetic strategy to 1,6-dihydropyridazines and pyridazines through Cu(II)-catalyzed controllable aerobic 6-endo-trig cyclization was developed. The selectivity can be rationally tuned via the judicious choice of reaction solvent.
Zhenwei Fan +3 more
semanticscholar +1 more source
A divergent synthetic strategy to 1,6-dihydropyridazines and pyridazines through Cu(II)-catalyzed controllable aerobic 6-endo-trig cyclization was developed. The selectivity can be rationally tuned via the judicious choice of reaction solvent.
Zhenwei Fan +3 more
semanticscholar +1 more source
Journal of Organic Chemistry, 2019
Switchable ring-contractive extrusion reactions of 2,5-dihydro-1,4,5-thiadiazepine S-oxides are described, which allow expedient access to pyridazines under thermal conditions or pyrazoles under Lewis acid-mediated conditions, respectively.
Bin Cheng +6 more
semanticscholar +1 more source
Switchable ring-contractive extrusion reactions of 2,5-dihydro-1,4,5-thiadiazepine S-oxides are described, which allow expedient access to pyridazines under thermal conditions or pyrazoles under Lewis acid-mediated conditions, respectively.
Bin Cheng +6 more
semanticscholar +1 more source
International Journal of Parasitology, 2018
The current therapeutic arsenal for toxoplasmosis is restricted to drugs non-specific to the parasite which cause important side effects. Development of more efficient and specific anti-Toxoplasma compounds is urgently needed.
Espérance Moine +11 more
semanticscholar +1 more source
The current therapeutic arsenal for toxoplasmosis is restricted to drugs non-specific to the parasite which cause important side effects. Development of more efficient and specific anti-Toxoplasma compounds is urgently needed.
Espérance Moine +11 more
semanticscholar +1 more source
ChemInform Abstract: Synthesis of Pyridazine and Fused Pyridazine.
ChemInform, 1995AbstractChemInform 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.
M. G. ASSY, E. A. EL‐GHANI
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Pyridazines. LXXXIV. Studies on borohydride reduction of pyridazine compounds
Journal of Heterocyclic Chemistry, 1976AbstractImidazo[1,2‐b]pyridazine, s‐triazolo[4,3‐b]pyridazine and tetrazolo[1,5‐b]pyridazine and some derivatives thereof were reduced with sodium borohydride to give the corresponding 5,6,7,8‐tetrahydro derivatives. A mechanism for these reductions is proposed and reduction at the C7‐C8 bond occurs before the reduction of the C6N5 bond.
P. K. Kadaba, B. Stanovnik, M. Tišler
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ChemInform Abstract: PYRIDAZINE 37. MITT. PYRIMIDO(1,2‐B)PYRIDAZINE
Chemischer Informationsdienst. Organische Chemie, 1971Abstract3‐Amino‐pyridazine (I) reagieren mit Acetessigestern (II) über die Zwischenstufen (III) beim Erhitzen in Polyphosphorsäure zu den Pyrimido(l ,2‐b)′‐′‐ pyridazin‐2‐onen (IV); der Grundkörper (IV) (R1 = CH3, R2 = H) kann auch mit Diketen (V) direkt erhalten werden.
A. POLLAK, B. STANOVNIK, M. TISLER
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Pyridazines. XXIII. A novel pyridazine into pyrazole ring transformation
Journal of Heterocyclic Chemistry, 1984AbstractTreatment of phenyl(4‐pyridazinyl)methanols 1a and 1b with p‐toluenesulfonic acid at elevated temperatures causes transformation into the C‐4 substituted pyrazole derivatives 8a and 8b. Limitations of this novel rearrangement reaction as well as mechanistic considerations are discussed.
Gottfried Heinisch, Richard Waglechner
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ChemInform, 2002
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.
Samia M. Sayed +3 more
openaire +1 more source
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.
Samia M. Sayed +3 more
openaire +1 more source

