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Table 4 1D and 2D-NMR data of 9 in DMSO (2.504 ppm-1H/39.4 ppm-13C) at 500 MHz

From: Comprehensive spectral identification of key intermediates to the final product of the chiral pool synthesis of radezolid

Atom position

δH [ppm], multiplicity, J HH or J HF [Hz]a

δC [ppm], J CF [Hz]a

HMBC correlations (H→C) a,b

2

153.8

4

3.73 (dd, 1H, J = 9.3, 6.6 Hz)

4.11 (dd, 1H, J = 9.0, 9.0 Hz)

47.0

2, 5, 6

2, 5, 6

5

4.72 (m, 1H)

71.7

2

6

3.41 (dd, 1H, J = 5.7, 5.7 Hz)

41.2

8, 5, 4

NHCOCH3

8.23 (t, 1H, J = 5.7)

8, 6

8

169.9

9

1.83 (s, 3H)

22.3

8

1′

140.3 (d, J CF  = 10.5 Hz)

2′

7.55 (dd, 1H, J = 10.9, 2.3 Hz)

105.2 (d, J CF  = 29.8 Hz)

3′, 6′, 4′, 1′

3′

161.1 (d, J CF  = 240.6 Hz)

4′

74.0 (d, J CF  = 21.2 Hz)

5′

7.83 (dd, 1H, J = 8.7, 7.7 Hz)

139.0 (d, J CF  = 3.4 Hz)

3′, 1′, 4′, 2′(w)

6′

7.19 (dd, 1H, J = 8.8, 2.4 Hz)

115.5 (d, J CF  = 2.9 Hz)

2′, 4′

  1. a s singlet, d doublet, dd doublet of doublets, t triplet, m multiplet, w weak
  2. bThis column gives the carbon atoms showing correlation with a given proton