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一个A环开环型芳基萘内酯类木脂素2D NMR全归属(英文) 被引量:1

NMR Assignments of A Ring A-seco Aryltetralin Lignan
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摘要 采用二维核磁共振技术(1 H-1 H COSY,DEPT,HSQC,HMBC,NOESY)和CD光谱,确定了A环开环型芳基萘内酯类木脂素3′,4′-O,O-demethylene-4-O-demethylpodophyllotoxin(1)的结构.首次对化合物1的13C NMR数据进行了全归属. The 13 C and 1H NMR chemical shifts of a ring A-seco aryltetralin lignan, 3',4'-O,O- demethylene-4-O-demethylpodophyUotoxin, were assigned based on 1D and 2D NMR data, in- cluding 1H-1H COSY, DEPT, HMBC, and HSQC. Stereochemistry was established based on 1H coupling constants (J values), NOESY results and circular dichroism (CD) results. The 13C NMR signals of the compound was completely assigned for the first time.
出处 《波谱学杂志》 CAS CSCD 北大核心 2013年第3期380-386,共7页 Chinese Journal of Magnetic Resonance
基金 Doctoral Science Foundation of Henan University of Traditional Chinese Medicine(BSJJ2011-13) the National Natural Science Foundation of China(30873363)
关键词 归属 2D NMR CD 芳基萘内酯类木脂素 NMR, assignment, 2D NMR, circular dichroism, aryltetralin lignans
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  • 1Casreo A, Del Corral J M, Gordaliza M, etal. Synthesis and cytotoxicity of podophyllotoxin analogues modified in the A ring[J]. Eur J Med Chem, 2003, 38(1): 65-74.
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  • 3Sun Y J, Li Z L, Chen H, et al. Three new cytotoxic arytetralin lignans from Sinopodophyllum emodi[J]. Bioorg Med Chem Lett, 2011, 21(12) : 3 794-3 797.
  • 4Wang Z Q, Hu H, Chen H X, et al. Antitumor agents. 124. New 413-substituted aniline derivatives of 6,7-O, O-demethylene-4'-O-demethylpodophyllotoxin and related compounds as potent inhibitors of human DNA topoi- someraseⅡ[J]. J MedChem, 1992, 35(5): 871-877.
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