表征数据: ¹H NMR (CDCl₃, 300 MHz) δ: 1.22-1.43 (1H, m, CH₂), 1.68-1.81 (6H, m, 3×CH₂), 1.82-1.95 (1H, m, CH₂), 2.31-2.37 (1H, dd, J=5.2, 11.9Hz, CH₂), 2.45-2.61 (6H, m, 3×CH₂, NH), 2.81-2.89 (1H, m, CH₂), 2.94-3.02 (1H, m, CH₂), 3.17-3.26 (1H, m, CH)；¹³C NMR (CDCl₃, 75.5MHz) δ: 23.4 (2×CH₂), 25.0, 30.1, 46.1 (3×CH₂), 54.6 (2×CH₂), 57.4 (CH), 62.1 (CH₂)；MS (ES+) m/z: 155 [(M+H)+, 100%]。
参考文献: [1] Journal of the American Chemical Society, 1987, vol. 109, p. 2040；[2] Bulletin of the Chemical Society of Japan, 1990, vol. 63, #3, p. 721-727；[3] Patent: US2003/195190, 2003, A1；[4] Patent: US4550107, 1985, A；[5] Organic Letters, 2009, vol. 11, #15, p. 3270-3273；[6] Tetrahedron Asymmetry, 2014, vol. 25, #4, p. 356-361
