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Nucleophilic substitution in aromatic compounds is feasible in substrates bearing strong electron-withdrawing substituents positioned ortho or para to the leaving group. The reaction proceeds via two steps: the addition of the nucleophile and the elimination of the leaving group.
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Anti-Nuclear Antibody Screening Using HEp-2 Cells
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[Seronegative spondylarthritis]

Peter Fasching

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    |July 16, 2010
    PubMed
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    No abstract available in PubMed .

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