Stereocontrolled transformations of trans alpha-beta aziridine aldehydes toward different amino hydroxylated structures
Academic Article
Publication Date:
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.
Iris type:
01.01 Articolo in rivista
Keywords:
aldol condensation; amino alcohols; amino diols; alpha-beta-aziridine aldehydes; alpha-furyl amides
List of contributors:
Righi, Giuliana
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