[1] William L, Shive M S. Synthesis of specifically 15N- and 13C-labeled a ntitumor (2-Haloethyl)nitrosoureas. The study of their conformations in solution by nitrogen-15 and carbon-13 nuclear magnetic resonance and evidence for stereoelectronic control in their aqueous decomposition[J]. J Org Chem, 1981, 46:5309-5321.[2] Su Jun(苏军), Meng Qing-wei(孟庆伟), Zhao Wei-jie(赵伟杰), et al. Synthesis of lomustine utilizing triphosgene(固体光气法合成洛莫司汀)[J]. Chinese J Med Chem(中国药物化学杂志), 2003, 13(3):170-171.[3] Jiang Hong(蒋虹), Wang Qiang(王强), Liu Xin-you(刘新友). A new derivative of hexahydroquinolin studied by NMR spectroscopy(一种新的六氢喹啉衍生物的NMR研究)[J]. Chinese J Magn Reson(波谱学杂志), 2007, 24(1):9-15.[4] Sun Wei(孙伟), Wei Yong-feng(魏永锋), Bai Yin-juan(白银娟), et al. An NMR study of α-mangostin(α-山竹黄酮的NMR研究)[J]. Chinese J Magn Reson(波谱学杂志), 2008, 25(2):257-264.[5] Zhao Yu-mei(赵玉梅), Liu Li-jun(刘力军), Miao Zhen-chun(缪振春). Structural determination of an aglycome by long-range DEPT and selective NOESY techniques(选择性远程DEPT和选择性NOESY技术用于苷类化合物的结构研究)[J]. Chinese J Magn Reson(波谱学杂志), 2008, 25(3):342-348.[6] Yang Xiu-wei(杨秀伟). Application of NMR for structural dedication of forbesoside(应用2D NMR技术研究羌活苷的结构)[J]. Chinese J Magn Reson(波谱学杂志), 2006, 23(4):429-441.[7] Tan Xiao-jian(谭小健), Wang Hai-Qing(王海顷), Jiang Hua-liang(蒋华良), et al. Structure assignment of 8α-OH phlegmariurine B(8α-OH马尾杉碱B的结构鉴定)[J]. Acta Chimica Sinica(化学学报), 2000, 58(11):1386-1392.[8] Zuo Ai-hua(左爱华), Chen Meng-chun(程孟春), Zhuo Rong-jie(卓荣杰), et al. Structure elucidation of degradation products of Z-ligustilide by UPLC-QTOF-MS and NMR spectroscopy(Z-藁本内酯降解产物的UPCL-QTOF-MS和NMR结构鉴定)[J]. Acta Pharmaceutica Sinica(药学学报), 2013, 48(6):911-916. |