alpha-Iminoesters are useful precursors to substituted alpha-amino acid derivatives and are utilized in a number of organic transformations. As a consequence of the adjacent ester functionality, these imines are more reactive relative to other types of imines. While a significant body of work has focused on nucleophilic additions to the imine carbon (C-alkylation), a second pathway that involves nucleophilic reaction at the nitrogen (N-alkylation) is much less explored. This tutorial review highlights work that has exploited this unusual alpha-iminoester reactivity mode.
机构:
Univ Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, FranceUniv Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, France
Chiev, KP
;
Roland, S
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Univ Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, FranceUniv Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, France
Roland, S
;
Mangeney, P
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Univ Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, FranceUniv Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, France
机构:
Univ Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, FranceUniv Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, France
Chiev, KP
;
Roland, S
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h-index: 0
机构:
Univ Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, FranceUniv Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, France
Roland, S
;
Mangeney, P
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, FranceUniv Paris 06, Lab Chim Organoelements, UMR 7611, F-75252 Paris 05, France