Table 1.
Nuclear magnetic resonance (NMR) spectroscopic data for compounds 1 and 2.
Position | 1 (CD3COCD3) | 2 (CDCl3) | ||
---|---|---|---|---|
δC | δ H | δ C | δ H | |
1 | 129.2 | 131.6 | ||
2 | 130.3 | 7.28, d (8.5) | 129.9 | 6.99, d (8.5) |
3 | 116.0 | 6.84, d (8.5) | 115.6 | 6.62, d (8.5) |
4 | 158.1 | 154.3 | ||
5 | 116.0 | 6.84, d (8.5) | 115.6 | 6.62, d (8.5) |
6 | 130.3 | 7.28, d (8.5) | 129.9 | 6.99, d (8.5) |
7 | 70.4 | 4.94, s | 35.6 | 4.41, s |
1′ | 135.1 | 130.2 | ||
2′ | 130.4 | 7.10, d (8.5) | 131.1 | 7.08, d (1.5) |
3′ | 115.6 | 6.89, d (8.5) | 127.6 | |
4′ | 158.2 | 153.7 | ||
5′ | 115.6 | 6.89, d (8.5) | 115.8 | 6.67, d (8.0) |
6′ | 130.4 | 7.10, d (8.5) | 128.0 | 7.06, dd (8.0, 1.5) |
7′ | 40.7 | 3.80, s | 72.8 | 3.85,s |
1″ | 133.5 | 65.9 | 3.57, q (7.0) | |
2″ | 130.5 | 7.02, d (8.0) | 15.3 | 1.24, t (7.0) |
3″ | 116.0 | 6.74, d (8.0) | ||
4″ | 156.5 | |||
5″ | 116.0 | 6.74, d (8.0) | ||
6″ | 130.5 | 7.02, d (8.0) |