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Enantiomeric N-tert-Butylsulfinyl Imines of Methyl Trifluoropyruvate: Promising Building Blocks in Asymmetric Synthesis of α-Trifluoromethylated Amino Acids and Derivatives

ChemistrySelect 2020, 5 (43), 13569-13574

DOI: 10.1002/slct.202003500

Cherednichenko A.; Bezgubenko L.; Rusanov E.; Onys'ko P.; Rassukana Y.

A convenient synthetic method for (R)- and (S)-N-tert-butylsulfinyl imines of methyl trifluoropyruvate has been developed. The synthetic potentialities of these chiral building blocks for the preparation of nonracemic trifluoroalanines, trifluoromethylated amino alcohols, β-nitro-α-amino acids, and pyrrolinone carboxylic acid derivatives have been demonstrated.

Enantiomeric N-tert-Butylsulfinyl Imines of Methyl Trifluoropyruvate: Promising Building Blocks in Asymmetric Synthesis of α-Trifluoromethylated Amino Acids and Derivatives

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