Table 1.
8 | 8a | ||||
---|---|---|---|---|---|
position | δC, type | δH (J in Hz) | δC, type | δH (J in Hz) | ΔδC(δ8a−δ8) |
1 | 144.9, C | 150.8, C | 5.9 | ||
2 | 142.7, C | 145.5, C | 2.8 | ||
3 | 111.3, C | 119.2, C | 7.9 | ||
4 | 116.3, CH | 7.37, d (2.2) | 116.9, CH | 7.40, d (2.2) | 0.6 |
5 | 111.8, C | 116.8, C | 5.0 | ||
6 | 129.5, CH | 6.54, d (2.2) | 129.4, CH | 6.49, d (2.2) | −0.1 |
1′ | 145.1, C | 148.5, C | 3.4 | ||
2′ | 138.8, C | 145.0, C | 6.2 | ||
3′ | 119.2, C | 119.4, C | 0.1 | ||
4′ | 149.0, C | 152.6, C | 3.6 | ||
5′ | 113.4, C | 113.5, C | 0.2 | ||
6′ | 114.2, C | 121.7, C | 7.5 | ||
−OH | 7.08, br s | ||||
−OH | 7.56, br s | ||||
1′-OCH3 | 61.6, CH3 | 3.79, s | |||
4′-OCH3 | 61.1, CH3 | 3.87, s | 61.0, CH3 | 3.91, s | |
2-OCH3 | 61.3, CH3 | 4.00, s |
Chemical shifts (δ) are referenced to residual CDCl3 (1H: 7.26/13C: 77.16 ppm).