In contrast to alkyl Grignard reagents, the allyl reagent reacts with nitroarenes via 1,2-addition to the nitro grouop. The 'in situ' treatment of the unstable intermediate adduct with LiAlH4 in the presence of catalytic Pd/C provides a general synthesis of N-allyl_N-arylhydroxylamines or N-allylanilines.

Unexpected reactivity of allyl magnesium chloride with nitroarenes. A general method of synthesis of N-allyl-N-arylhydroxylamines and N-allylanilines

MARCANTONI, Enrico;
1988-01-01

Abstract

In contrast to alkyl Grignard reagents, the allyl reagent reacts with nitroarenes via 1,2-addition to the nitro grouop. The 'in situ' treatment of the unstable intermediate adduct with LiAlH4 in the presence of catalytic Pd/C provides a general synthesis of N-allyl_N-arylhydroxylamines or N-allylanilines.
1988
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/241837
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