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Volumn 15, Issue 24, 2009, Pages 6008-6014

Facile and efficient enantioselective strecker reaction of ketimines by chiral sodium phosphate

Author keywords

Asymmetric catalysis; Enantioselectivity; Ketimines; Sodium; Strecker reaction

Indexed keywords

ASYMMETRIC CATALYSIS; ASYMMETRIC INDUCTION; BINAPHTHYL; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE; IN-SITU; KETIMINES; METAL SALT; REACTIVE NUCLEOPHILES; SODIUM PHOSPHATE; STRECKER REACTION; STRECKER REACTIONS; TRIMETHYLSILYL CYANIDE; WORKING MODELS;

EID: 66349105583     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900210     Document Type: Article
Times cited : (100)

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    • In our previous study of the Strecker reaction of aldimines, 1H NMR spectroscopic data suggested that the N atom of the imine probably coordinated to the silicon atom of the hypervalent silicate and ultimately formed an NèSi bond see the following ref, Z. G. Jiao, X. M. Feng, B. Liu, F. X. Chen, G. L. Zhang, Y. Z. Jiang, Eur. J. Org. Chem. 2003, 3818, According to refs, 2c, k] the product appeared to be silylated 2 in the reaction mixture and the silyl ether was hydrolyzed during the aqueous workup or direct silica gel chromatography
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