Cobalt(II) complexes of chiral bis-binaphthyl porphyrins were prepared, and their catalytic activity in the asymmetric cyclopropanation of alkenes with ethyl diazoacetate was examined. Good yields and enantioselectivities (up to 90% ee) were observed with cis/trans ratios reaching 11:89. UV-vis and 1H NMR studies suggest that the axial nitrogen ligand N-methylimidazole could play a role in changing the enantioselectivity of the reaction.

Asymmetric cyclopropanation of olefins catalyzed by chiral cobalt(II)-binaphthyl porphyrins / S. Fantauzzi, E. Gallo, E. Rose, N. Raoul, A. Caselli, S. Issa, F. Ragaini, S. Cenini. - In: ORGANOMETALLICS. - ISSN 0276-7333. - 27:23(2008), pp. 6143-6151.

Asymmetric cyclopropanation of olefins catalyzed by chiral cobalt(II)-binaphthyl porphyrins

S. Fantauzzi
Primo
;
E. Gallo
Secondo
;
A. Caselli;F. Ragaini
Penultimo
;
S. Cenini
Ultimo
2008

Abstract

Cobalt(II) complexes of chiral bis-binaphthyl porphyrins were prepared, and their catalytic activity in the asymmetric cyclopropanation of alkenes with ethyl diazoacetate was examined. Good yields and enantioselectivities (up to 90% ee) were observed with cis/trans ratios reaching 11:89. UV-vis and 1H NMR studies suggest that the axial nitrogen ligand N-methylimidazole could play a role in changing the enantioselectivity of the reaction.
Enantioselective cyclopropanation; rutheneium porphyrins; metalloporphyrin catalysts; theoretical-analysis; amination reactions; trans-selectivity; terminal olefins; carbine complex; iron-porphyrin; ligand-design
Settore CHIM/03 - Chimica Generale e Inorganica
2008
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/56608
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