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The authors identify a cluster of proteins that target human complement and bind plasminogen, revealing a conserved structural fold and a multifunctional immune evasion strategy that enables survival of Borrelia recurrentis in the human host.
(R)-(+)-tert-Butylsulfinamide achieves stereoselective reactions by condensing with carbonyl groups to form sulfinyl imine intermediates, and after the reaction, this group can be removed under acidic conditions to obtain the target product
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