Skip to main content

Table 2 13C NMR Chemical Shifts (ppm) (125

From: Synthesis of lipophilic tyrosyl esters derivatives and assessment of their antimicrobial and antileishmania activities

  (Ty) (TyC2) (TyC3) (TyC8) (TyC10) (TyC12) (TyC16) (TyC18) (TyC18: 1)
1 63.1 65.7 65.6 65.9 65.3 63.7 65.6 65.6 65.7
2 37.2 34.6 34.6 34.6 34.4 32.7 34.8 34.8 35.0
3 130.6 130.2 130.12 129.6 129.9 127.5 129.9 129.9 130.9
4 131.3 130.4 130.41 130.3 129.4 128.2 130.3 130.3 130.07
5 115.7 115.8 115.7 115.9 115.4 113.7 115.7 115.7 116.1
6 154.1 154.8 154.8 155.2 154.7 153.1 154.9 154.9 155.4
1'   171.9 174.1 175.4 174.7 173.1 174.9 174.4 174.6
2'   21.4 30.09 34.8 34.3 32.7 34.6 34.6 32.6
3'    28.04 25.3 31.9 23.2 25.3 25.34 25.7
4'     29.4-29.2 29.4-29.1 27.9-27.4 29.5-30.1 29.5-30.1 29.8-28.0
(CH2)3     29.4-29.2 29.4-29.1 27.9-27.4 29.5-30.1 29.5-30.1 29.8-28.0
8'     14.4 24.8 27.9-27.4 29.5-30.1 29.5-30.1 27.2
9'      22.6 27.9-27.4 29.5-30.1 29.5-30.1 129.8
10'      14.1 32.5 29.5-30.1 29.5-30.1 128.0
11'       21.0 29.5-30.1 29.5-30.1 27.2
12'       12.43 29.5-30.1 29.5-30.1 29.8-28.0
13'        29.5-30.1 29.5-30.1 29.8-28.0
14'        32.3 29.5-30.1 29.8-28.0
15'        23.1 29.5-30.1 29.8-28.0
16'        14.5 32.3 31.9
17'         23.09 23.4
18'         14.5 14.8