A new synthesis of both enantiomers of protected 4-oxopipecolic acid was achieved in six steps via 1,3-dipolar cycloaddition of C-ethoxycarbonyl N-(1R)-phenylethylnitrone to but-3-en-1-ol.
Practical synthesis of both enantiomers of protected 4-oxopipecolic acid
Machetti Fabrizio;Brandi Alberto
2001
Abstract
A new synthesis of both enantiomers of protected 4-oxopipecolic acid was achieved in six steps via 1,3-dipolar cycloaddition of C-ethoxycarbonyl N-(1R)-phenylethylnitrone to but-3-en-1-ol.File in questo prodotto:
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