“…The solution was stirred at ambient temperature overnight and concentrated in vacuo to give a residue that was subjected to a silica gel column chromatography (methylene chloride/methanol, 96/4) to give the desired product as white solid (0.74 g, 82%). 1 H NMR (300 MHz, CDCl 3 , δ ): 7.54 (s, 1H), 7.03 (d, J = 0.9 Hz, 1H), 6.94 (t, J = 1.2 Hz, 1H), 6.21 (t, J = 5.7 Hz, 1H), 3.98 (t, J = 6.9 Hz, 2H), 3.24 (q, J = 6.6 Hz, 2H), 2.21 (t, J = 6.9 Hz, 4H), 2.14 (t, J = 7.8 Hz, 2H), 1.98 (quint, J = 6.6 Hz, 2H), 1.61-1.24 (m, 28H), 0.86 (t, J = 6.9 Hz, 3H); 13 3.00 mmol) in 10 mL methylene chloride was added to a solution of 2,5-dioxopyrrolidin-1-yl heptadeca-4,6-diynoate (HDDA-NHS, 0.72 g, 2.00 mmol) and TEA (0.41 g, 4 mmol) in 10 mL of methylene chloride. The solution was stirred at ambient temperature overnight and concentrated in vacuo to give a residue that was subjected to a silica gel column chromatography (methylene chloride/methanol, 96/4) to give the desired product as yellow liquid (0.57 g, 77%).…”