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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 1319-1325 
    ISSN: 1434-193X
    Keywords: Asymmetric synthesis ; Tetrahydroisoquinolines ; Cyclizations ; Diastereoselective alkylation of Amides ; Phenylglycinol ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Bischler-Napieralski cyclisation of optically active β-substituted phenylethylamines 4a-c followed by diastereoselective reduction led to 1,4-disubstituted tetrahydroisoquinolines 6a-c and 8a-c. The same methodology afforded the 4-benzyl pyrroloisoquinolines 10.
    Type of Medium: Electronic Resource
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