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. 2020 Feb 6;25(3):707. doi: 10.3390/molecules25030707

Table 1.

Electronic circular dichroism (ECD) (Δε) and UV (ε) data for derivatives 1, 311 measured in cyclohexane solution.

Compd. ECD [Δε (nm)] UV [ε (nm)]
1a −9.0 (228); 2.9 (215); −0.1 (208); 47.0 (197); −41.8 (185) 70,500 (194)
1b −8.0 (229); 1.9 (214); 50.4 (197); −41.8 (186) 67,500 (194)
1c −6.3 (232); 45.6 (200); −52.8 (185)a 67,800 (194)
1d −5.0 (229); 2.6 (217); −9.1 (207); 43.4 (196); −31.1 (186) 69,700 (194)
1e −6.2 (233); 52.5 (201); −62.3 (186) 67,400 (194)
3 2.4 (241); −20.2 (207); 14.0 (185)a 8,000 (236); 73,300 (193)
4 1.4 (296); −0.8 (265); 6.0 (235); −25.7 (205); 47.5 (185)a 1,200 (265); 74,500 (190)
5 −5.9 (235); 41.4 (205); −28.0 (185)a 70,600 (194)
6 1.0 (240); −8.5 (222); −14.7 (204); 20.9 (185)a 8,400 (236); 76,100 (193)
7 b −2.9 (238); −3.7 (220); 4.3 (207); −2.9 (197); 8.5 (185)a 59,700 (193)
8 −2.5 (238); 3.2 (220); 11.4 (207); −6.5 (191) 5,500 (248); 83,600 (193)
9 −14.6 (235); 83.3 (207); −92.4 (192) 147,000 (192)
10 +5.0 (238); −24.0 (204); 45.0 (185)a 20,000 (238); 135,000 (193)
11 −7.0 (226); 32.3 (200); −24.0 (185)a 77,900 (197)

[a] end of measuring range; [b] partially insoluble in cyclohexane.