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Volumn 44, Issue 19, 2003, Pages 3805-3808

N-Salicyl-β-aminoalcohols as a new class of ligand for catalytic asymmetric Strecker reactions

Author keywords

Catalytic asymmetric synthesis; Imines; Strecker

Indexed keywords

ALCOHOL DERIVATIVE; AMINONITRILE; BENZYLAMINE DERIVATIVE; CYANIDE; IMINE; LIGAND; N BENZYLIDENEBENZYLAMINE; NITRILE; TRIMETHYLSILYLCYANIDE; UNCLASSIFIED DRUG;

EID: 0037420767     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00735-4     Document Type: Article
Times cited : (37)

References (32)
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    • Prepared in 68% yield as a white crystalline solid by reduction of
    • 4 reduction of the salicylimine derived from an α-amino ester. See: Narasimhan S., Balakumar R. Synth. Commun. 30:2000;4387-4396.
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    • note
    • 3- 4a catalyst system at 10 mol%.
  • 30
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    • note
    • 4- 4a gave a completely racemic product 2a . However, if the concentration of HCN was kept low at all time by slow addition of the HCN solution to 1a under the same conditions, (S)-2a was obtained in 94% yield and 63% ee.
  • 31
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    • note
    • αH signals.
  • 32
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    • note
    • 13C NMR and elemental analyses.


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