Nitrosocarbonyl intermediates, generated at r.t. by the mild oxidation of nitrile oxides, undergo clean ene reactions with tetramethyl- and trimethyl-ethylene and with cyclohexene. With less substituted ethylenes the ene pathway is still active but the oxidation step of the nitrile oxides competes with the cycloadditions to the olefins.

Nitrosocarbonyl Intermediates as Super-Enophiles: a Mild Method for Carbon-Nitrogen Bond Formation

QUADRELLI, PAOLO;MELLA, MARIELLA;CARAMELLA, PIERLUIGI
1998

Abstract

Nitrosocarbonyl intermediates, generated at r.t. by the mild oxidation of nitrile oxides, undergo clean ene reactions with tetramethyl- and trimethyl-ethylene and with cyclohexene. With less substituted ethylenes the ene pathway is still active but the oxidation step of the nitrile oxides competes with the cycloadditions to the olefins.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/116066
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