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8-O-4′型异木脂素立体构型的测定方法
引用本文:原忠,李铣.8-O-4′型异木脂素立体构型的测定方法[J].波谱学杂志,2003,20(3):307-314.
作者姓名:原忠  李铣
作者单位:沈阳药科大学中药学院28#信箱,辽宁沈阳 110016
摘    要:综述了关于8-O-4′型异木脂素的立体化学方面的研究. 总结了测定8-O-4′型异木脂素的相对构型和绝对构型的常用方法. 1H NMR谱是研究C-7 和C-8间相对构型的常用方法, 若H-7的偶合常数较小,在2.7~5.0 Hz范围内,为赤式;若H-7的偶合常数较大,在6.0~8.6 Hz范围内,则为苏式. 结合NOE差谱以及CD谱的测定,或者Mosher's法,可进一步阐明其绝对构型.

关 键 词:核磁共振    8-O-4′型异木脂素    立体构型    CD谱    NOE差谱    Mosher's法  
文章编号:1000-4556(2003)03-0307-08
收稿时间:2003-03-31
修稿时间:2003年3月31日

NMR METHODS FOR DETERMINING THE CONFIGURATION OF 8-O-4'NEOLIGNANS
YUAN Zhong,LI Xian.NMR METHODS FOR DETERMINING THE CONFIGURATION OF 8-O-4''''NEOLIGNANS[J].Chinese Journal of Magnetic Resonance,2003,20(3):307-314.
Authors:YUAN Zhong  LI Xian
Institution:School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, P.O. Box 28#, Shenyang 110016, China
Abstract:The NMR methods for determining the relative and absolute configurations of 8-O-4′Neolignans were reviewed. The relative stereochemistry between C-7
and C-8 should be in theerythro form if the coupling constant between the measured by 1H NMR is small (J=2.7~5.0 Hz). If the coupling constant me
asured is larger (J=6.0~8.6 Hz), the configuration is in the threo form. With the application of NOE difference spectroscopy, CD assay and Mosher's method, the absolute configuration can be determined.
Keywords:NMR  8-O-4′Neolignans  configuration  NOE difference spectroscopy  CD spectroscopy  Mosher's method  
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