1,3-Diazetidinones are obtained by bis(dibenzylideneacetone)palladium(0)-catalyzed carbonylation of diaziridines having one substituent attached to the ring carbon atom. This regiospecific insertion into the nitrogen-nitrogen bond also occurs for 3,3-disubstituted diaziridines, provided one uses stoichiometric quantities of cobalt carbonyl.

Regiospecific synthesis of aza-.beta.-lactams from diaziridines / H. Alper, D. Delledonne, M. Kameyama, D. Roberto. - In: ORGANOMETALLICS. - ISSN 0276-7333. - 9:3(1990), pp. 762-765.

Regiospecific synthesis of aza-.beta.-lactams from diaziridines

D. Roberto
Ultimo
1990

Abstract

1,3-Diazetidinones are obtained by bis(dibenzylideneacetone)palladium(0)-catalyzed carbonylation of diaziridines having one substituent attached to the ring carbon atom. This regiospecific insertion into the nitrogen-nitrogen bond also occurs for 3,3-disubstituted diaziridines, provided one uses stoichiometric quantities of cobalt carbonyl.
Settore CHIM/03 - Chimica Generale e Inorganica
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/193856
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