Rapid assembly of anti,anti-1,2,3-triol motifs via stereoselective addition of organometallics to aldehydes obtained from (R′,R′,S,R)-2,3-butane diacetal protected butanetetraol derivatives

D. J. Dixon, L. Krause, S. V. Ley

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A predictable stereoselective method for the synthesis of enantiopure anti, anti-1,2,3-triols through the addition of organometallic reagents to the axially disposed aldehyde derived from (R′,R′,S,R)-2,3-butane diacetal protected butanetetraol is described.
    Original languageEnglish
    Pages (from-to)2516-2518
    Number of pages2
    JournalJournal of the Chemical Society. Perkin Transactions 1
    Issue number20
    DOIs
    Publication statusPublished - 2001

    Keywords

    • Addition reaction; Asymmetric synthesis and induction (rapid assembly of anti,anti-1,2,3-triol motifs via stereoselective addn. of organometallics to aldehydes obtained from (R',R',S,R)-2,3-butane diacetal protected butanetetraol derivs.); Alcohols Role: PNU (Preparation, unclassified), PREP (Preparation) (trihydric, 1,2,3-; rapid assembly of anti,anti-1,2,3-triol motifs via stereoselective addn. of organometallics to aldehydes obtained from (R',R',S,R)-2,3-butane diacetal protected butanetetraol derivs.)

    Fingerprint

    Dive into the research topics of 'Rapid assembly of anti,anti-1,2,3-triol motifs via stereoselective addition of organometallics to aldehydes obtained from (R′,R′,S,R)-2,3-butane diacetal protected butanetetraol derivatives'. Together they form a unique fingerprint.

    Cite this