Results 1 to 10 of about 317 (127)
Synthesis of 2H-azirine-2,2-dicarboxylic acids and their derivatives [PDF]
Beilstein Journal of Organic ChemistryMethods for the preparation of 3-aryl-2H-azirine-2,2-dicarboxylic acids and their amides, esters, and azides by FeCl2-catalyzed isomerization of 3-aryl-5-chloroisoxazole-4-carbonyl chlorides into 3-aryl-2H-azirine-2,2-dicarbonyl dichlorides followed by ...
Anastasiya V. Agafonova +2 more
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3-Aryl-2H-azirines as annulation reagents in the Ni(II)-catalyzed synthesis of 1H-benzo[4,5]thieno[3,2-b]pyrroles [PDF]
Beilstein Journal of Organic ChemistryA high-yielding method for the synthesis of 3-arylbenzo[4,5]thieno[3,2-b]pyrroles has been developed via pyrrole ring annulation to the aromatic benzo[b]thiophene system, using 3-arylazirines as a N‒C=C synthon.
Julia I. Pavlenko +5 more
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3-Amino-2H-azirine, Moleküle mit vielfältigen Reaktionsmöglichkeiten
CHIMIA, 1979 3-Amino-2H-azirines, cyclic three-membered amidines with an estimated ring strain of about 200 kJ/mole, undergo a variety of reactions. Thereby, each of the azirine bonds can be broken: Thermolysis leads to the rupture of the C(2),C(3)-bond, with strong
Heinz Heimgartner
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2H-Azirines as dipolarophiles [PDF]
Tetrahedron Letters, 2003 AbstractFor Abstract see ChemInform Abstract in Full Text.
Melo, Teresa M. V. D. Pinho e +3 more
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Synthesis of 2-halo-2H-azirines [PDF]
Tetrahedron, 2001 Abstract α-Oxophosphonium ylides react with N -chlorosuccinimide, N -bromosuccinimide and N -iodosuccinimide in the presence of azidotrimethylsilane giving the corresponding haloazidoalkenes which were completely converted to the 2-halo-2 H -azirines on heating in heptane.
Pinho e Melo, Teresa M. V. D. +3 more
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Reactivity of 2-halo-2H-azirines. Part 3: Dehalogenation of 2-halo-2H-azirine-2-carboxylates [PDF]
Tetrahedron, 2003 AbstractFor Abstract see ChemInform Abstract in Full Text.
Pinho e Melo, Teresa M. V. D. +2 more
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Access to highly substituted oxazoles by the reaction of α-azidochalcone with potassium thiocyanate
Beilstein Journal of Organic Chemistry, 2020 The reactivity of α-azidochalcones has been explored for the preparation of highly substituted oxazoles via a 2H-azirine intermediate. The azidochalcones, when treated with potassium thiocyanate in the presence of potassium persulfate, lead to 2,4,5 ...
Mysore Bhyrappa Harisha +4 more
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Photochemische Cycloaddition von 3-Phenyl-2H-azirinen mit Ketenen
CHIMIA, 1972 Irradiation of 2,2-dimethyl-3-phenyl- (1c) and 2,3-diphenyl-2H-azirine (1d) in benzene solution in the presence of ketene (5) yields 2,2-dimethyl-4-phenyl- (6) and 2,4-diphenyl-5-methylen-3-oxazoline (7), respectively. Similar cycloadducts (9a to d) are
H. Heimgartner +6 more
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Stabile Zink-Komplexe von 3-Amino-2H-azirinen
CHIMIA, 1978 3-Dimethylamino-2,2-dimethyl-2H-azirine (4a), which is known to react easily with Brönsted acids and electrophiles, forms a stable complex 5a with ZnBr2. In contrast to all other reactions of 4a, the three-membered ring in this complex is preserved. The
Kurt Dietliker +3 more
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Bildung eines Azacyclols durch transanulare Ringkontraktion
CHIMIA, 1988 Reaction of 3-dimethylamino-2,2-dimethyl-2H-azirine (1) with phthalimide (8) in polar solvents yields the (1:1)-adduct 2-dimethylamino-9b-hydroxy-3,3-dimethyl-5,9b-dihydro-3H-imidazo[2,1-a]isoindol-5-one (10).
Marlise Schläpfer-Dähler +4 more
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