Treatment of 2,3,3-triphenyl-4-formylisoxazolidines with bases triggers an unprecedented anionic reactional cascade which terminates with a 2-iminooxetane derivative. In the case of 2,3,3-triphenyl-4-methoxycarbonyl isoxazolidine the multistep rearrangement gives rise to a derivative of malonic acid.

New base induced rearrangements of 4-acylisoxazolidines. Anionic reactional cascades from five membered rings to either four membered rings or open chain compounds

Oberti Roberta;
1996

Abstract

Treatment of 2,3,3-triphenyl-4-formylisoxazolidines with bases triggers an unprecedented anionic reactional cascade which terminates with a 2-iminooxetane derivative. In the case of 2,3,3-triphenyl-4-methoxycarbonyl isoxazolidine the multistep rearrangement gives rise to a derivative of malonic acid.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/248391
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