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The release of repulsive interactions of steric and/or stereoelectronic nature and the onset of a new extended and effective conjugation concur to an unprecedented and sythetically appealing shift of a nitro group from the β- to the α-position with respect to the aryl group of a styrene moiety. © 2007 Bentham Science Publishers Ltd.

Bianchi, L., Giorgi, G., Maccagno, M., Petrillo, G., Rizzato, E., Spinelli, D., et al. (2007). An Unprecedented “Reverse” 1,2 Migration of a Nitro Group within an α-Aryl-β-nitroethenyl Moiety Driven by Steric and Stereoelectronic Effects. LETTERS IN ORGANIC CHEMISTRY, 4(4), 268-272 [10.2174/157017807781024165].

An Unprecedented “Reverse” 1,2 Migration of a Nitro Group within an α-Aryl-β-nitroethenyl Moiety Driven by Steric and Stereoelectronic Effects

Giorgi G.;
2007-01-01

Abstract

The release of repulsive interactions of steric and/or stereoelectronic nature and the onset of a new extended and effective conjugation concur to an unprecedented and sythetically appealing shift of a nitro group from the β- to the α-position with respect to the aryl group of a styrene moiety. © 2007 Bentham Science Publishers Ltd.
2007
LETTERS IN ORGANIC CHEMISTRY
Bianchi, L., Giorgi, G., Maccagno, M., Petrillo, G., Rizzato, E., Spinelli, D., et al. (2007). An Unprecedented “Reverse” 1,2 Migration of a Nitro Group within an α-Aryl-β-nitroethenyl Moiety Driven by Steric and Stereoelectronic Effects. LETTERS IN ORGANIC CHEMISTRY, 4(4), 268-272 [10.2174/157017807781024165].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/10061
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