Publication: Übergangsmetall-katalysierte Additionsreaktionen von 3-Phenyl-2H-azirinen und Acetylencarbonsäureestern
Übergangsmetall-katalysierte Additionsreaktionen von 3-Phenyl-2H-azirinen und Acetylencarbonsäureestern
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Inada, A., & Heimgartner, H. (1982). Übergangsmetall-katalysierte Additionsreaktionen von 3-Phenyl-2H-azirinen und Acetylencarbonsäureestern. Helvetica Chimica Acta, 65(5), 1489–1498. https://doi.org/10.1002/hlca.19820650523
Abstract
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Transition Metal Catalyzed Addition Reactions of 3-Phenyl-2H-azirines and Alkyl Acetylene Carboxylates. In the presence of molybdenum hexacarbonyl, the 3-phenyl-2H-azirines 1 and 7 react with alkyl acetylene carboxylates 2 via the cleavage of the C,N-double bond to give 2H-pyrroles 5 or pyrrole 9 (Table), whose structures were deduced from the spectra data, in particular 13C-NMR data. The 2H-pyrrole 5a was also obtained by treatment of a mixture of 1 and 2a with tungsten hexachloride. A tentative mechanism for the formation of the 2H-
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- Inada, Akira
- Heimgartner, Heinz
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Inada, A., & Heimgartner, H. (1982). Übergangsmetall-katalysierte Additionsreaktionen von 3-Phenyl-2H-azirinen und Acetylencarbonsäureestern. Helvetica Chimica Acta, 65(5), 1489–1498. https://doi.org/10.1002/hlca.19820650523
