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. 2020 Jul 30;15(17):1661–1671. doi: 10.1002/cmdc.202000260

Table 5.

NMR data of teicoplanin derivatives.

graphic file with name CMDC-15-1661-g005.jpg

15

16

17

18

1H

13C

1H

13C

1H

13C

1H

13C

y1

174.36

173.79

n.d.

173.47

y7

170.02

169.90

169.67

169.94

y4

169.68

169.44

169.67

169.37

y2

169.36

169.25

169.17

169.19

y5

169.00

168.87

168.58

168.83

y3

168.33

168.22

167.16

168.17

y6

167.46

167.30

166.53

167.30

C=O(NAc) G7

165.94

165.58

n.d.

165.59

3c

158.56

158.46

159.90

158.45

7e

157.75

157.65

158.51

157.60

3e

156.87

156.75

158.24

156.73

7c

155.75

155.62

157.05

155.67

5d

155.61

155.49

155.95

155.44

2d

151.16

151.07

155.95

151.04

6d

149.21

149.10

151.15

149.08

4c

148.96

148.83

149.53

148.77

4e

148.02

147.93

148.13

147.91

1d

147.49

147.42

147.60

147.40

triazole‐q (4)

143.78

143.76

143.59

143.75

6a

142.74

142.60

142.19

142.61

1c

140.94

140.89

139.09

140.83

3a

139.49

139.68

138.17

139.37

7a

138.62

138.64

135.18

138.60

5b

7.12

136.1

7.12

136.01

7.17. 7.09

136.3

7.11

135.97

2a

135.41

135.3

135.18

135.30

4d

134.43

134.74

n.d.

134.31

1a

n.d.

134.36

n.d.

n.d.

2b

7.21

131

7.2

130.91

7.15

130.24

7.21

130.94

2f

7.94

130.6

7.89

130.46

7.72

131.25

7.92

130.44

4a

127.22

127.13

126.81

128.6

6c

126.7

126.59

126.71

128

6f

7.26

127.81

7.28

127.8

7.25

127.74

7.27

128

6b

7.86

128.49

7.87

128.35

7.81

128.29

7.87

128.37

2c

125.43

125.33

n.d.

127.13

5a

125.43

125.33

n.d.

126.59

5f

6.67

125.12

6.66

125.29

6.65

125.02

6.66

125.32

1f

6.9

125.59

6.9

125.48

7.04

124.33

6.9

125.48

2e

7.19

124.84

7.18

124.72

7.08

127.15

7.19

124.73

6e

6.99

119.0

6.96

118.94

7.24

123

7.27

123.05

triazole‐CH (5)

7.74

123.98

7.71

123.81

7.7

123.88

7.72

123.78

5c

122.17

122.19

122.2

122.06

1e

7.26

123.24

7.25

123.06

6.89

118.61

7.05

119.37

7b

117.82

117.71

117.87

117.71

1b

7.04

119.49

7.04

119.39

6.94

119.6

6.97

118.91

5e

6.65

116.45

6.64

116.38

6.65

116.32

6.64

116.37

3b

6.34

110.03

6.34

109.97

6.32

109.53

6.34

109.97

4b

5.5

108.05

5.56

107.92

5.54

107.65

5.56

108

7f

6.5

107.86

6.52

107.92

6.53

107.73

6.48

107.68

3d

6.38

105.1

6.37

104.97

6.34

104.17

6.37

104.99

4f

5.1

104.59

5.1

104.46

5.09

104.26

5.1

104.47

3f

6.55

104.02

6.55

103.84

6.57

103.39

6.55

103.85

7d

6.32

101.68

6.3

101.51

6.31

101.52

6.3

101.56

G1

4.38

99.27

4.4

98.73

4.37

99.42

4.42

98.57

G5

3.1

76.79

3.11

76.77

3.09

76.44

3.11

76.77

G3

5.4

76.14

5.45

75.58

5.35

76.2

5.44

75.43

G4

3.39

73.38

3.4

73.4

3.4

72.89

3.41

73.4

z6

3.22

70.02

3.25

69.97

3.26

69.13

3.23

70.05

x6

4.16

60.94

4.15

60.88

4.2

60.46

4.14

60.87

G6

3.62

60.25

3.6

60.29

3.39

60.1

3.6

60.38

x3

5.4

58.31

5.41

58.21

5.36

58.41

5.41

58.17

x1

4.33

59.28

4.33

59.22

4.28

59.08

4.36

58.9

x7

7.12

64.04

7.09

64.03

7.06

64.18

7.1

63.98

G2

3.52

55.8

3.52

55.9

3.59

55.23

3.51

55.98

x4

5.65

54.67

5.63

54.65

5.6

54.27

5.64

54.64

x2

4.87

55.46

4.89

55.37

4.97

55

4.88

55.38

x5

4.37

53.61

4.37

53.53

4.38

53.22

4.36

53.54

z2,2’

n.d.

n.d.

3.32, 2.92

36.18

Side chain

OCH2 (a)

4.45

63.29

4.45

63.25

4.45

63.04

4.45

63.23

OCH2

3.48

69.34

3.48

69.32

3.48

69.07

3.5

69.67

OCH2

3.51

68.9

3.51

69.08

3.51

68.62

3.5

69.38

OCH2

3.44

68.48

3.44

68.5

3.44

68.24

3.46

68.48

3.5

68.39

CH2 (e)

1.73

20.25

1.73

20.26

CH2 (f)

2.24

26.76

2.23

26.87

CH2 (k)

1.76

20.23

1.76

20.24

CH2 (l)

2.23

26.86

2.28

26.85