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mrdone.0907

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13C NMR (101 MHz, CDCl3) ¦Ä               
13.69,14.97,22.86,25.33,27.44,27.78,30.92,30.95,38.94,82.41,127.05,129.87,135.58,143.26,157.20,194.21
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mrdone.0907: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¬£¬ 2013-09-21 10:39:48
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1 .     mandolin W
C15H22O2     ÏàËÆ¶È:93.7%
Journal of Natural Products          2001          64          71-74
Constituents of the Roots and Stems of Aristolochia mollissima
Tian-Shung Wu, Yu-Yi Chan, and Yann-Lii Leu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     7-O-ethylmadolin W
C17H26O2     ÏàËÆ¶È:70.5%
Journal of Natural Products          2013          76          664-671
Extracellular Signal-Regulated Kinases (ERK) Inhibitors from Aristolochia yunnanensis
Zhong-Bin Cheng, Wei-Wei Shao, Ye-Na Liu, Qiong Liao, Ting-Ting Lin, Xiao-Yan Shen, and Sheng Yin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     cis-neocniditide
    ÏàËÆ¶È:62.5%
Planta Medica          1987          53          77-80
cis- and trans-Neocnidilide; 1H- and '3C-NMR Data of Some Phthalides
Frederik C. Fischer1 and Marion J. M. Gijbels
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4-(non-4-en-2-yl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine
C16H25NS     ÏàËÆ¶È:62.5%
Heterocycles          2010          81          1903-1921
An Efficient and Convenient Synthesis of 4,5,6,7-Tetrahydrothieno[3,2-c]pyridines by a Modified Pictet-Spengler Reaction via a Formyliminium Ion Intermediate
Michikazu Kitabatake, Aki Hashimoto, Toshiaki Saitoh, Takehiro Sano, Kunihiko Mohri, and Yoshie Horiguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-Pheny-5-[(8R,11Z)-8-Hydroxyheptadec-11-enyl]-1H-1,2,4-triazole
    ÏàËÆ¶È:62.5%
Archiv der Pharmazie          2008          341          714-720
Synthesis,Antibacterial and Antifungal Activity of Some Novel 3,5-Disubstituted-1H-1,2,4-triazoles
Shweta Sharma, Saloni Gangal, Abdul Rauf and Maryam Zahin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     neolaurencenyne
C15H22     ÏàËÆ¶È:62.5%
Tetrahedron letters          1981          22          4729-4732
Laurencenyne, a plausible precursor of various nonterpenoid C15-compounds, and neolaurencenyne from the red alga laurencia okamurai
Hideo Kigoshi, Yoshikazu Shizuri, Haruki Niwa, Kiyoyuki Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     neolaurencenyne
C15H22     ÏàËÆ¶È:62.5%
Tetrahedron          1986          42          3781-3787
Four new C15 acetylenic polyenes of biogenetic significance from the red alga : Laurencia okamurai: structures and synthesis
Hideo Kigoshi, Yoshikazu Shizuri, Haruki Niwa, Kiyoyuki Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1-[(1E)-1-propyl(2-2H)pent-1-en-1-yl](2-2H)-cyclooctene
C16H26D2     ÏàËÆ¶È:62.5%
Russian Journal of Organic Chemistry          2008          44          1291-1295
Intermolecular cycloalumination of cyclic and acyclic alkynes with Et n AlCl3− n in the presence of Cp2ZrCl2
V. A. D¡¯yakonov, L. F. Galimova, A. G. Ibragimov and U. M. Dzhemilev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (S)-2-pentyl-1-tosylaziridine-2-carbaldehyde
C15H21NO3S     ÏàËÆ¶È:62.5%
European Journal of Organic Chemistry          2011                   4046-4052
Organocatalyzed Aziridination of -Branched Enals: Enantioselective Synthesis of Aziridines with a Quaternary Stereo-center
Alaric Desmarchelier, Danilo Pereira de Sant'Ana, Vincent Terrasson, Jean Marc Campagne, Xavier Moreau, Christine Greck and Renata Marcia de Figueiredo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     madolin W (S)-MTPA ester
    ÏàËÆ¶È:62.5%
Journal of Natural Products          2013          76          664-671
Extracellular Signal-Regulated Kinases (ERK) Inhibitors from Aristolochia yunnanensis
Zhong-Bin Cheng, Wei-Wei Shao, Ye-Na Liu, Qiong Liao, Ting-Ting Lin, Xiao-Yan Shen, and Sheng Yin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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