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. Author manuscript; available in PMC: 2015 Feb 4.
Published in final edited form as: Org Biomol Chem. 2010 Apr 21;8(8):1773–1776. doi: 10.1039/c000905a

Fig. 2.

Fig. 2

Representative crude HPLC traces for conversion of N-allylamine 7 to amide 8 with different coupling agents as described in Table 3. Peptide was deprotected and cleaved from Rink amide resin with TFA, and monitored at 220 nm. (a) N-allyl peptide, (b) PyBrOP/DMAP, (c) TFFH/HOAt, (d) HATU/HOAt, (e) DIC/HOAt, (f) triphosgene.