The stereocontrolled condensation of methyl ketones to trans alpha,beta-aziridine aldehydes creates functionalized aldols, valuable precursors for different amino hydroxylated structures, such as amino alcohols, amino diols, alpha-tetrahydrofuryl amides, and alpha-furyl amides.
Stereocontrolled transformations of trans alpha-beta aziridine aldehydes toward different amino hydroxylated structures
Righi Giuliana;
2006
Abstract
The stereocontrolled condensation of methyl ketones to trans alpha,beta-aziridine aldehydes creates functionalized aldols, valuable precursors for different amino hydroxylated structures, such as amino alcohols, amino diols, alpha-tetrahydrofuryl amides, and alpha-furyl amides.File in questo prodotto:
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