Isoxazolidines, nitrogen-oxygen bond

Several isoxazolidines or their quaternary salts derived from the 1,3-dipolar cycloaddition of rr/i-hcxcnolidcs (6,7-dihydrooxepin-2(5//)-ones) to cyclic nitrones, were converted into the corresponding piperidyl- and pyrrolidyloxepi-nones by reduction of the nitrogen-oxygen bond (Equation 4). These amino alcohols provide a new access to the l-azabicyclo[5.3.0]decane core of the Stemona alkaloids <2004EJ04215>. 

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