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Synlett 1994; 1994(3): 165-166
DOI: 10.1055/s-1994-22777
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A Highly Stereoselective Synthesis of the N-Terminal Amino Acid Analogue of Nikkomycin B and Bx

Chisato Mukai* , Motonori Miyakawa, Miyoji Hanaoka
  • *Faculty of Pharmaceutical Sciences, Kanazawa University, Takara-machi, Kanazawa 920, Japan
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Publikationsdatum:
22. März 2002 (online)

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A novel procedure for a highly stereoselective preparation of an analogue of the N-terminal amino acid moiety of nikkomycin B and Bx was developed on the basis of a highly diastereoselective aldol reaction of chiral chromium(0)-complexed benzaldehyde derivative.