1H NMR Reassignment for Z/E-Benzomalvins B and Absolute Configuration of Benzomalvin C

被引:0
|
作者
Rong Chao
Yan-Wei Wu
Ling Lu
Wei-Feng Xu
Chang-Yun Wang
Chang-Lun Shao
机构
[1] Ocean University of China,Key Laboratory of Marine Drugs, The Ministry of Education of China, School of Medicine and Pharmacy
来源
关键词
sp.; benzomalvins; –; isomerisation; X-ray single crystal diffraction;
D O I
暂无
中图分类号
学科分类号
摘要
Benzomalvins B, C, and E (1, 2, and 3) were simultaneously obtained from the marine fungus Aspergillus sp. isolated from the soft coral Sinularia sp., collected from South China Sea. Their structures were elucidated on the basis of NMR spectroscopic data and by comprehensive comparison with those previously reported in the literature. The stability of the double bond of E-benzomalvin B (1) under different light conditions was investigated, and 1 was transformed to Z-benzomalvin B (1′) with UV 365 nm irradiation. In particular, the incorrect 1H NMR data of 1′ in the literature was reassigned for the first time. Moreover, the absolute configuration of benzomalvin C (2) was also reported for the first time by X-ray single crystal diffraction.
引用
收藏
页码:343 / 345
页数:2
相关论文
共 50 条
  • [1] 1H NMR Reassignment for Z/E-Benzomalvins B and Absolute Configuration of Benzomalvin C
    Chao, Rong
    Wu, Yan-Wei
    Lu, Ling
    Xu, Wei-Feng
    Wang, Chang-Yun
    Shao, Chang-Lun
    CHEMISTRY OF NATURAL COMPOUNDS, 2021, 57 (02) : 343 - 345
  • [2] Chiral thiols:: The assignment of their absolute configuration by 1H NMR
    Porto, Silvia
    Manuel Seco, Jose
    Ortiz, Aurelio
    Quinoa, Emilio
    Riguera, Ricardo
    ORGANIC LETTERS, 2007, 9 (24) : 5015 - 5018
  • [3] Absolute Configuration and 1H NMR Characterization of Rosmaridiphenol Diacetate
    Munoz, Marcelo A.
    Perez-Hernandez, Nury
    Pertino, Mariano W.
    Schmeda-Hirschmann, Guillermo
    Joseph-Nathan, Pedro
    JOURNAL OF NATURAL PRODUCTS, 2012, 75 (04): : 779 - 783
  • [4] Utilization of 1H NMR in the determination of absolute configuration of alcohols
    Barreiros, Marizeth L.
    David, Jorge M.
    David, Juceni P.
    QUIMICA NOVA, 2005, 28 (06): : 1061 - 1065
  • [5] Total structural assignment and absolute configuration of terreinol by 13C and 1H NMR
    de Macedo, FC
    Marsaioli, AJ
    MAGNETIC RESONANCE IN CHEMISTRY, 2005, 43 (03) : 251 - 255
  • [6] Assignment of the absolute configuration of α-chiral carboxylic acids by 1H NMR spectroscopy
    Ferreiro, MJ
    Latypov, SK
    Quiñoá, E
    Riguera, R
    JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (09): : 2658 - 2666
  • [7] Absolute Configuration Determination for Natural Products (II)-Absolute Configuration Determination for Alkaloids by Comparing Computed Optical Rotations, 13C NMR and 1H NMR with the Experimental Results
    Hu Dongbao
    Zhou Beidou
    CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2016, 37 (11): : 1993 - 1998
  • [8] Reassignment of the 1H NMR spectrum of fusidic acid and total assignment of 1H and 13C NMR spectra of some selected fusidane derivatives
    Rastrup-Andersen, N
    Duvold, T
    MAGNETIC RESONANCE IN CHEMISTRY, 2002, 40 (07) : 471 - 473
  • [9] Role of barium(II) in the determination of the absolute configuration of chiral amines by 1H NMR spectroscopy
    García, R
    Seco, JM
    Vázquez, SA
    Quiñoá, E
    Riguera, R
    JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (03): : 1119 - 1130
  • [10] An Approach for Determining the Absolute Configuration of C-2 in 2-Oxygenated Phenylethanoid Glycosides by 1H NMR Spectroscopy
    Shao, Si-Yuan
    Zhang, Fan
    Yang, Ya-Nan
    Feng, Zi-Ming
    Jiang, Jian-Shuang
    Zhang, Pei-Cheng
    ORGANIC LETTERS, 2016, 18 (16) : 4084 - 4087