EFFICIENT ASYMMETRIC INDUCTION VIA COORDINATION OF CHIRAL DIAMINE TO TIN(II) ENOLATE: A HIGHLY ENANTIOSELECTIVE SYNTHESIS OF 2-SUBSTITUTED MALATES

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<jats:title>Abstract</jats:title> <jats:p>In the presence of chiral diamine, (2S)-1-methyl-2-[(N-1-naphthylamino)methyl]pyrrolidine, the tin(II) enolate of 3-acetylthiazolidine-2-thione reacts with various α-ketoesters to afford the corresponding aldol-type products, generally, in greater than 95% enantiomeric excess.</jats:p>

収録刊行物

  • Chemistry Letters

    Chemistry Letters 12 (11), 1799-1802, 1983-11

    Oxford University Press (OUP)

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