A New, Versatile and Stereospecific Route to Unusual Amino Acids: The Enantiospecific Total Synthesis of Statine Amide and Its Three Stereoisomers

DOI: 10.1021/jo00042a026

Source and publish data:

Journal of Organic Chemistry p. 4441 - 4444 (1992)

Update date:2022-08-03

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Authors:

Bessodes, M.

Saiah, M.

Antonakis, K.

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Article abstract of DOI:10.1021/jo00042a026

Total syntheses of statine amide <(3S,4S)-4-amino-3-hydroxy-6-methylheptanamide> and its three stereoisomers are described in order to illustrate the versatility of a new route to β-hydroxy-γ-amino acids.The enantioselective Sharpless epoxidation of a rac

Full text of DOI:10.1021/jo00042a026

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