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13 C NMR ÈܼÁ CDCl3 18.3,20.0,20.5,23.3,24.6,27.8,28.5,30.0,45.5,55.0,61.6,75.9,79.8,82.1,88.1,97.0,99.3,122.8,134.2,157.5,163.1,164.3,212.5 |
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½10¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . trans-erioaustrasine ÏàËÆ¶È:54.1% Phytochemistry 2001 58 329-332 3-Monoterpenyl-2,4-dioxygenated quinoline alkaloids from the aerial parts of Halfordia kendack Nasim Sultana, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . terreulactone A C28H30O9 ÏàËÆ¶È:53.8% Tetrahedron Letters 2002 43 3197-3198 Terreulactone A, a novel meroterpenoid with anti-acetylcholinesterase activity from Aspergillus terreus Won-Gon Kim, Kyung-Mi Cho, Chong-Kil Lee, Ick-Dong Yoo Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . tert-butyldiphenyl[(4S)-1-(tetrahydro-2H-pyran-2-yloxy)oct-2-yn-4-yloxy]silane ÏàËÆ¶È:52.1% European Journal of Organic Chemistry 2011 4460-4464 Stereoselective Total Synthesis of Umuravumbolide Vanam Shekhar, Dorigondla Kumar Reddy, Sudina Purushotham Reddy, Peddikotla Prabhakar and Yenamandra Venkateswarlu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (1R,3aR,5S,7aR)-1-((R)-1,5-dimethylhexyl)-5-(2,6-dimethylmorpholine-4-yl)-3a,7a-dimethyloctahydroinden-4-one ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2013 21 1925-1943 Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase Mathias König, Christoph M¨¹ller, Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . tert-butyl (1S,3R,5S,6S)-6-((S)-2-(tert-butoxycarbonyl-amino)-propanamido)-3-(2,6-dichlorophenyl)-5-isopropyl-1-methyl-7-oxohexahydropyrazolo[1,2-a]pyrazole-1-carboxylate C29H42Cl2N4O6 ÏàËÆ¶È:52.1% Tetrahedron 2013 69 6648-6665 Synthesis of pyrazolo[1,2-a]pyrazole-based peptide mimetics Ana Novak, Ana Testen, Jure Bezenšek, Uroš Grošelj, Martina Hrast, Marta Kasunič, Stanislav Gobec, Branko Stanovnik, Jurij Svete Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (3S,7ar)-6-[2-(2-bromo-6-methoxy-4-methylphenyl)ethyl]-7a-isobutyl-3-isopropyltetrahydropyrrolo[2,1-b]-oxazol-5-one C23H34BrNO3 ÏàËÆ¶È:52.1% The Journal of Organic Chemistry 2004 69 2773-2784 Synthesis of (()-Hamigeran B, (-)-Hamigeran B, and (()-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon-Oxygen Bond from Hydrogenolysis Derrick L. J. Clive and Jian Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 21 C24H34O8 ÏàËÆ¶È:52.1% Tetrahedron Letters 2012 53 45-47 Formal synthesis of (+)-didemniserinolipid B Bodugam Mahipal, Kundarapu Mallikarjun, Srivari Chandrasekhar Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . isoterreulactone A C28H32O8 ÏàËÆ¶È:52% Bioorganic & Medicinal Chemistry Letters 2005 15 353-356 Isoterreulactone A, a novel meroterpenoid with anti-acetylcholinesterase activity produced by Aspergillus terreus Ick-Dong Yoo, Kyung-Mi Cho, Chong-Kil Lee, Won-Gon Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (2S)-6[2(3-hydroxyisopropyl)-5-methyl-4-hexenyl]-5-methoxy-7,2',4'-trihydroxyflavanone C26H32O7 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2008 46 903-906 Structural determination of flavonoids from Sorphora flavescens (pages 903¨C906) Xiao-Chi Ma, Xiu-Lan Xin, Bao-Jing Zhang, Feng-Yun Li, Ke-Xin Liu and De-An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . terreulactone A C28H30O9 ÏàËÆ¶È:50% The Journal of Antibiotics 2003 56 351-357 Terreulactones A, B, C, and D: Novel Acetylcholinesterase Inhibitors Produced by Aspergillus terreus II. Physico-chemical Properties and Structure Determination WON-GON KIM,KYUNG-MI CHO,CHONG-KIL LEE and ICK-DONG YOO Structure 13C NMR ̼Æ×Ä£Äâͼ |

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