Title of article :
Asymmetric synthesis of α,β-substituted β-aminoalkanamides and stereochemical determination
Author/Authors :
Capriati، نويسنده , , Vito and Degennaro، نويسنده , , Leonardo and Florio، نويسنده , , Saverio and Luisi، نويسنده , , Renzo and Cuocci، نويسنده , , Corrado، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Pages :
4
From page :
8655
To page :
8658
Abstract :
Highly enantiomerically enriched β-aminoalkanamides 12 and β-phenylaminoalkanamides 13 have been prepared by the addition reaction of α-lithiated 2-alkyl-2-oxazolines 9-Li, derived from optically active oxazolines 9, to N-cumyl nitrones 2. The relative stereochemistry of alkanamides 5 and 6 has been established by 1D-NOESY experiments carried out on the related pyrimidinones 7, whereas the absolute configuration of alkanamides 12 and 13 has been confirmed by an X-ray analysis.
Keywords :
Nitrones , lithiation , Oxazolines , amino acids , asymmetric synthesis
Journal title :
Tetrahedron Letters
Serial Year :
2007
Journal title :
Tetrahedron Letters
Record number :
1857451
Link To Document :
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