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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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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
13 .     cyclolaudenyl formate
C32H52O2     ÏàËÆ¶È:80%
Journal of Natural Products          2001          64          953-955
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