Table 1.
10R (K)-trans-anti-[BP]G | Intermolecular NOEs |
---|---|
H1 (7.63 ppm) | MeC5(H6)[m], MeC5(H1′)[w], MeC5(H2′)[m], MeC5(H2′′)[w], MeC5(CH3)[m], G6(H2′′)[w], C7(H5)[m], C7(H6)[w], G16(H1)[m] |
H2 (7.63 ppm) | MeC5(NH2)[m], MeC5(H6)[m], MeC5(CH3)[m], C7(NH2)[m], G16(H1)[m] |
H3 (7.40 ppm) | MeC5(NH2)[m], MeC5(CH3)[w], G16(H1)[m], G18(H1)[w] |
H4 (6.79 ppm) | G16(H1)[m], G18(H1)[w] |
H5 (6.74 ppm) | G16(H1)[w], G18(H1)[w] |
H6 (7.32 ppm) | T8(H4′)[m], G16(H1)[w], G18(H1)[m], G18(H1′)[m] |
H7 (5.14 ppm) | C7(H1′)[m], T8(H4′)[m] |
H8 (4.36 ppm) | A19(H4′ ′)[m] |
H9 (4.48 ppm) | G6(H1)[m], G6(H1′)[w] |
H10 (6.48 ppm) | G18(H1)[w], G6(H1)[m], G6(H2′′), C7(H1′)[m], C7(H4′)[m] |
H11 (7.96 ppm) | MeC5(H1′)[m], MeC5(H1′′)[m], G6(H1)[m], C7(H5)[w], C7(H1′)[m] |
H12 (7.48 ppm) | MeC5(H1′)[m], MeC5(H2′)[m], MeC5(H2′′′)[m], MeC5(H6)[m], MeC5(CH3)[w], G6(H2′)[m], G6(H2′′)[m], C7(H6)[m], C7(H5)[m], C7(H1′)[w] |
NH (11.23 ppm) | MeC5(H1′)[m] |
The chemical shifts of the adduct were recorded at 0 °C in H2O and 2H2O buffered solutions.