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J Org Chem ; 65(25): 8704-8, 2000 Dec 15.
Article in English | MEDLINE | ID: mdl-11112592

ABSTRACT

Addition of Et(2)AlCN and i-PrOH to ketosulfinimines (N-sulfinyl imines) affords corresponding alpha-alkyl alpha-amino nitriles in moderate to good yields. The diastereoselectivity is largely dependent on the E/Z isomer ratio of the ketosulfinimine. Hydrolysis of the diastereomerically pure amino nitriles affords enantiopure alpha-alkyl alpha-amino acids in moderate to good yields.


Subject(s)
Amino Acids/chemical synthesis , Sulfonium Compounds/chemistry , Imines/chemistry , Magnetic Resonance Spectroscopy
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