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Table 2 Comparison of chemical shift and coupling constant values of MOM-protected munduserol [43], elliptinol [38, 39], 6a, 12a-cis-12, 12a-cis-12-acetoxy-6,6a,12,12a-tetrahydrorotoxen [44], compound (1) and (2)

From: Study on the absolute configuration and biological activity of rotenoids from the leaves and twigs of Millettia pyrrhocarpa Mattapha, Forest & Hawkins, sp. Nov

Position

MOM-protected munduserol

[43]

(J in Hz)

Elliptinol

[38]

(J in Hz)

Elliptinol

[39]

(J in Hz)

6a, 12a-cis-12, 12a-cis-12-acetoxy-6,6a,12,12a-Tetrahydrorotoxen [44] (J in Hz)

Compound (1) (J in Hz)

Compound (2) (J in Hz)

6a

4.84, d, (3.3)

5.00, br.ddd

4.94, m

4.92, dd, (5.1, 5.2 Hz)

4.33, dt (10.2, 4.3)

4.16, td, (4.3, 10.0)

12a

3.96, s

3.65, br.dd

3.48 t, (4.8)

3.65, dd, (5.1, 5.3)

3.15, t (10.2)

3.04, t, 10.0)

12

5.05, s

6.44, br.d

5.04, d, (4.8)

6.38, d, (5.3)

4.98, t (10.2)

4.74, d, (10.0)