“…The 1 H and 13 C NMR chemical shifts (Table 1) of compounds 2 and 1 were almost superimposable. The 1 H NMR spectrum of 2 exhibited signals at δ 7.87 (brd, J = 8.2 Hz, H-7′); 7.16 (ddd, J = 1.3, 7.2, 8.2 Hz, H-6′); 7.08 (ddd, J = 1.2, 7.2, 7.9 Hz, H-5′), 7.67 (brd, J = 7.9 Hz, H-4′) amd 7.46 (brs, H-2′), characteristic of tryptophan derivatives [24,26,27]. The 13 C NMR spectrum showed a downfield shift of C-2 in compound 2 with respect to compound 1 (73.8 ppm in 2 vs 56.2 ppm in 1 ), suggesting the presence of an OH group at C-2 in compound 2 instead of the NH 2 group present in 1 .…”