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mrdone.0907½ð³æ (ÕýʽдÊÖ)
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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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yangliguo007
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mrdone.0907: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¬£¬ 2013-09-21 10:39:48
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mrdone.0907: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¬£¬ 2013-09-21 10:39:48
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²éѯ½á¹û£º¹²²éµ½350¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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