After the cyclization step, the quinoline derivatives are cleaved from the solid support. This is typically done using reagents that selectively remove the resin and any protecting groups, leaving behind the desired 2,6-disubstituted quinoline derivatives.
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Pentanoic acid, 5-(3-formyl-4-nitrophenoxy)-
cyclo[Ala-Pro-D-PheΨ{(C=S)NH}-Ser-Thr(rprenyl)-Ser(rprenyl)-Ile]
