Once the desired cyclic oligomer is constructed on the solid support, any protecting groups used during synthesis are removed to reveal the free functional groups. Finally, the cyclic oligomer is cleaved from the resin. This step typically involves treatment with an appropriate cleavage reagent, and the resulting product is collected.
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C52H42O4Si2
(R)-3-{(S)-2-[(S)-6-Benzyloxycarbonylamino-2-(2-tert-butoxycarbonylamino-acetylamino)-hexanoylamino]-3-methyl-butyrylamino}-tetradecanoic acid
phenyl 6-O-tert-butyldimethylsilyl-2,3,4-tri-O-4-methoxybenzyl-1-thio-α-D-mannopyranoside
