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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 509-514 
    ISSN: 1434-193X
    Keywords: Azasugars ; Pyrrolo-oxazolidinones ; Amidoalkylation ; Sakurai reaction ; Asymmetric synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydroxy-substituted pyrrolidines are important structural elements in azasugars. Effective precursors for such compounds are pyrrolo-oxazolidinones of type 1. Short asymmetric syntheses starting from easily available low-priced precursors are desirable. Two efficient pathways to these structures starting from the 4-methoxylated oxazolidinones 2 and 3, easily accessible from the chiral pool, have been successfully developed. These oxazolidinones can be used as amidoalkylation reagents. Via Sakurai reactions and subsequent intramolecular cyclization, the synthesis of bicyclic pyrrolidines is possible in a stereocontrolled way.
    Type of Medium: Electronic Resource
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