Research Article
Microbial Transformations of 7-Hydroxyflavanone
Table 2
13C NMR chemical shifts (δ) of compounds 1 ÷ 6.
| Carbon | Compounds | 1a | 2b | 3b | 4b | 5b | 6c |
| C-2 | 81.1 | 80.2 | 80.0 | 77.0 | 73.8 | 162.8 | C-3 | 45.2 | 44.3 | 44.2 | 40.3 | 37.8 | 106.6 | C-4 | 193.1 | 192.2 | 190.8 | 65.6 | 59.5 | 176.4 | C-5 | 129.9 | 129.7 | 128.8 | 128.3 | 159.7 | 126.5 | C-6 | 111.9 | 110.1 | 110.3 | 108.8 | 92.0 | 115.1 | C-7 | 166.9 | 168.0 | 166.2 | 156.3 | 161.5 | 161.9 | C-8 | 103.9 | 100.9 | 100.9 | 103.0 | 93.5 | 102.6 | C-9 | 165.4 | 162.2 | 163.6 | 155.4 | 156.5 | 157.5 | C-10 | 115.1 | 126.2 | 114.7 | 118.7 | 106.3 | 116.1 | C-1′ | 140.7 | 130.3 | 138.7 | 140.4 | 141.0 | 131.3 | C-2′ | 127.4 | 127.9 | 115.5 | 126.0 | 126.3 | 126.2 | C-3′ | 129.7 | 130.1 | 135.2 | 128.7 | 128.8 | 129.1 | C-4′ | 129.6 | 128.8 | 135.4 | 128.3 | 128.1 | 131.6 | C-5′ | 129.7 | 130.1 | 115.4 | 128.7 | 128.8 | 129.1 | C-6′ | 127.4 | 127.9 | 115.9 | 126.0 | 126.3 | 126.2 | OCH3 | | 55.7 | 55.6 | | | |
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aSolvent CD3OD.
bSolvent CDCl3.
cSolvent DMSO-d6.
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