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        Synlett 1998; 1998(8): 843-844
DOI: 10.1055/s-1998-1793
   DOI: 10.1055/s-1998-1793
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      data processing and storage.Highly syn-Diastereoselective Synthesis of NH-3-Benzyloxy-4-aryl-azetidin-2-ones via a Two-Step Staudinger Reaction
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   Publication History
Publication Date:
31 December 2000 (online)
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New conditions for the Staudinger reaction provide NH-3-benzyloxy-4-aryl-β-lactams in good yields with complete cis-diastereoselectivity.
Staudinger - isoserine - paclitaxel - azadiene
 
    