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13CNMR(100MHz,CDCl3):15.7,16.0,16.4,16.6,18.3,21.4,21.5,22.0,23.8,25.1,28.1,29.2,31.4,33.3,33.4,34.1,35.4,37.2,38.0,38.9,40.6,45.4,45.5,47.3,47.8,47.9,49.5,50.9,56.1,81.0,106.3,107.5,153.0,156.1,171.1 [ Last edited by ׿Խ_ÏÈ·æ on 2015-6-7 at 13:35 ] |
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²éѯ½á¹û£º¹²²éµ½14920¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (24S)-24-methyl-dammara-20,25-diene-3¦Â-yl-acetate C33H54O2 ÏàËÆ¶È:88.5% Phytochemistry 1998 49 441-449 Phytotoxic compounds from Esenbeckia yaxhoob Rachel Mat¦Á, Martha L Mac¨ªas, Irma S Rojas, Blas Lotina-Hennsen, Ruben Alfredo Toscano, Ana Luisa Anaya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,28-di-O-acetyl-30-N-(dodecylamino)-lup-20(29)-ene C46H79NO4 ÏàËÆ¶È:83.7% Chemistry of Natural Compounds 2004 40 571-573 SYNTHESIS OF 30-AMINO DERIVATIVES OF 3,28-DI-O-ACETYLBETULIN O. B. Flekhter, I. E. Smirnova, F. Z. Galin,G. V. Giniyatullina E. V. Tret'yakova,and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-Acetoxy-28-oxo-28-[3-acetyl-(3-aminopropyl)-amino]lup-20(29)-ene C37H60N2O2 ÏàËÆ¶È:83.7% Russian Journal of Bioorganic Chemistry 2013 39 329-337 Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 15a ÏàËÆ¶È:82.8% Chemical & Pharmaceutical Bulletin 1996 44 1748-1753 Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3,25 diacetylderivative of 3¦Â,20,25-trihydroxylupane ÏàËÆ¶È:82.8% Phytochemistry 1998 48 863-866 Triterpenes from Rhus taitensis Aysen Y¨¹r¨¹ker, Jimmy Orjala, Otto Sticher, Topul Rali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 24-Methylene-26-acetoxycycloartan-3-one ÏàËÆ¶È:82.8% Phytochemistry 1996 42 795-798 A cycloartane triterpenoid and ¦Ø-phenyl alkanoic and alkenoic acids from Trichilia claussenii Mônica T. Pupo, Paulo C. Vieira, João B. Fernandes, M. F¨¢tima das G. F. da Silva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 24-methyl-dammara-20,25-diene-3¦Â-yl-acetate C33H54O2 ÏàËÆ¶È:82.8% Journal of Ethnopharmacology 2015 160 52−60 Alkaline phosphataseactivity-guidedisolationofactivecompounds and newdammarane-typetriterpenesfrom Cissus quadrangularis hexaneextract Thanika Pathomwichaiwat, PanneeOchareon, NoppamasSoonthornchareonnon, Zulfiqar Ali, IkhlasA.Khan, SompopPrathanturarug Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3,28-di-O-acetyl-30-N-(pentadodecylamino)-lup-20(29)-ene C49H85NO4 ÏàËÆ¶È:81.5% Chemistry of Natural Compounds 2004 40 571-573 SYNTHESIS OF 30-AMINO DERIVATIVES OF 3,28-DI-O-ACETYLBETULIN O. B. Flekhter, I. E. Smirnova, F. Z. Galin,G. V. Giniyatullina E. V. Tret'yakova,and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 2¦Â-(1-Oxobutoxy)olean-12-en-28-oic acid C34H54O4 ÏàËÆ¶È:80% Journal of Natural Products 2009 72 1414-1418 Synthesis of 3-Deoxypentacyclic Triterpene Derivatives as Inhibitors of Glycogen Phosphorylase Pu Zhang,Jia Hao,Jun Liu,Qian Lu, Huaming Sheng, Luyong Zhang, and Hongbin Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . pachymic acid ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2008 56(10) 1459-1462 13CCytotoxic and Anti-oxidant Activities of Lanostane-Type Triterpenes Isolated from Poria cocos Liang ZHOU,Yaochun ZHANG,Leslie Adell GAPTER,Hui LING,Rajesh AGARWAL,and Ka-yun NG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â,16¦Â-Diacetoxybetulinic acid methyl ester C35H54O6 ÏàËÆ¶È:80% Phytochemistry 2007 68 591-595 ¦Á-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae) Luc Meva¡¯a Mbaze, Herve Martial P. Poumale , Jean Duplex Wansi,Jean Alexandre Lado, Shamsun Nahar Khan, Muhammad Choudhary Iqbal,Bonaventure Tchaleu Ngadjui, Hartmut Laatsch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 5b C33H54O2 ÏàËÆ¶È:80% Phytochemistry 2003 591-596 Triterpenoids from the orchids Agrostophyllum brevipes and Agrostophyllum callosum P.L. Majumder, S. Majumder, S. Sen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . cyclolaudenyl formate C32H52O2 ÏàËÆ¶È:80% Journal of Natural Products 2001 64 953-955 |

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