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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