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16.61,16.74,17.23,17.28,17.46,17.49,18.60,21.17,23.43,23.50,23.66,24.65,25.92,28.02,28.38,29.10,30.71,30.82,32.94,33.01,33.25,33.95,37.20,38.18,38.29,
39.15,39.56,39.62,39.77,41.73,41.95,42.28,46.17,46.41,47.51,47.78,47.91,53.26,55.65,68.33,83.56,122.21,122.73,123.57,125.29,135.59,139.04,144.60,
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12.94, 20.11, 21.30, 21.51, 23.82, 27.67, 29.32, 31.63, 32.16, 33.05, 33.23, 33.38, 35.10, 48.46,50.65, 52.21,55.62, ,69.24, 108.77,111.55, 125.87,129.53, 130.21,138.58, 145.14,147.61, 151.00,151.30,169.67,173.43,178.03,196.80
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1 .     caryocaroside IV-6
    ÏàËÆ¶È:61.2%
Journal of Natural Products          2006          69(2)          196-205
Triterpenoid Saponins from the Fruits of Caryocar glabrum
Abdulmagid Alabdul Magid, Laurence Voutquenne, Christian Moretti, Christophe Long, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     leonticin E prosapogenin
    ÏàËÆ¶È:61.2%
Phytochemistry          1997          44          497-504
Leonticins D-H, five triterpene saponins from Leontice kiangnanensis
Min Chen, Wei Wei Wu, Daniel Nanz, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     compound 5
C51H82O17     ÏàËÆ¶È:60%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     auriculatusaponin B
C46H66O11     ÏàËÆ¶È:59.1%
Planta Medica          1998          64          50-53
Triterpenoid Saponins from Aster auriculatus
Chang Zeng Wang and De Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     araloside D
    ÏàËÆ¶È:59.1%
Acta Pharmaceutica Sinica          1991          26          197-202
STUDIES ON THE SAPONINS FROM THE ROOT BARK OF A RALIA CHINENSIS L.
WJ Sun; DK Zhang; ZF Sha; HL Zhang and XL Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Bifinoside B
C48H76O18     ÏàËÆ¶È:59.1%
Chemical & Pharmaceutical Bulletin          2011          59          1417-1420
Oleanolic Triterpene Saponins from the Roots of Panax bipinnatifidus
Nguyen Huu TUNG, Tran Hong QUANG, Nguyen Thi Thanh NGAN, Chau Van MINH, Bui Kim ANH, Pham Quoc LONG, Nguyen Manh CUONG, and Young Ho KIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 8
C52H84O17     ÏàËÆ¶È:58.8%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     compound 10
C52H84O18     ÏàËÆ¶È:58.8%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 6
C57H82O16     ÏàËÆ¶È:58%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     3¦Â-O-[¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-olean-12-en-28-O-[(3-O-acetyl)-¦Á-L-rhamnopyranosyl]ester
C50H80O18     ÏàËÆ¶È:58%
Natural Product Communications          2012          7          1427-1430
Antiproliferative Oleanane Saponins from Dizygotheca elegantissima
Antonio Vassallo, Mariasabina Pesca, Letizia Ambrosio, Nicola Malafronte, Nadia Dekdouk Melle, Fabrizio Dal Piaz and Lorella Severino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     caryocaroside IV-5
    ÏàËÆ¶È:57.1%
Journal of Natural Products          2006          69(2)          196-205
Triterpenoid Saponins from the Fruits of Caryocar glabrum
Abdulmagid Alabdul Magid, Laurence Voutquenne, Christian Moretti, Christophe Long, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     compound 9
C47H76O16     ÏàËÆ¶È:57.1%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     lotoidoside E
C44H71NO13     ÏàËÆ¶È:57.1%
Planta Medica          2005          71          554-560
Antiproliferative Hopane and Oleanane Glycosides from the Roots of Glinus lotoides
Arafa I. Hamed,Sonia Piacente, Giuseppina Autore,Stefania Marzocco,Cosimo Pizza,Wieslaw Oleszek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     araloside A
    ÏàËÆ¶È:57.1%
Acta Pharmaceutica Sinica          1991          26          197-202
STUDIES ON THE SAPONINS FROM THE ROOT BARK OF A RALIA CHINENSIS L.
WJ Sun; DK Zhang; ZF Sha; HL Zhang and XL Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     guaiacin B
    ÏàËÆ¶È:57.1%
Phytochemistry          1999          51          1049-1053
Triterpenoid saponins from Fagonia indica
Kamel H. Shaker, Mirko Bernhardt, M. Hani A. Elgamal, Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     nudicaucin B
    ÏàËÆ¶È:57.1%
Phytochemistry          1998          48          525-528
Triterpenoid saponins from Hedyotis nudicaulis
Masataka Konishi, Yoshio Hano, Mitsuo Takayama, Taro Nomura, Ahmad Sazali Hamzah, Rohaya bte Ahmad, Halila Jasmani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     3-O-[¦Á-L-rhamnopyranosyl (1¡ú3)-¦Â-D-glucuronopyranosyl]-28-O-[¦Â-D-glucopyranosyl]-3¦Â-hydroxyolean-12-en-oate
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1990          Vol 53          466
A New Saponin from Deeringia amaranthoides
O. P. Sati, S. Bahuguna, S. Uniyal, J. Sakakibara, T. Kaiya, A. Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Bidenoside B
C46H72O18     ÏàËÆ¶È:57.1%
Zeitschrift f¨¹r Naturforschung B          2004          59b          821-824
Triterpene Saponins from Knautia integrifolia var. bidens
Özgen Alankuş-Çalışkan, Safiye Emirdağ, Erdal Bedir, Sibel Avunduk, and H¨¹seyin Anıl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     akeboside Ste
    ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2004          35          495-498
ÈýҶľͨÌÙ¾¥µÄ»¯Ñ§³É·ÖÑо¿
ÍõêÊ,³¾²,ÁÖÈð³¬
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     3-O-[¦Â-D-glucopyranosyl-(1¡ú2)]-¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-arabinosyl oleanolic acid
    ÏàËÆ¶È:57.1%
Zeitschrift f¨¹r Naturforschung C          2007          62          661-667
Phytochemical and Molluscicidal Investigations of Fagonia arabica
E. A. El-Wakil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     3¦Â-O-[¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-olean-12-en-28-O-[¦Á-L-rhamnopyranosyl]ester
C48H78O17     ÏàËÆ¶È:57.1%
Natural Product Communications          2012          7          1427-1430
Antiproliferative Oleanane Saponins from Dizygotheca elegantissima
Antonio Vassallo, Mariasabina Pesca, Letizia Ambrosio, Nicola Malafronte, Nadia Dekdouk Melle, Fabrizio Dal Piaz and Lorella Severino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




22 .     3-O-¦Á-L-rhamnopyranosyl (1¡ú2)-¦Â-D-glucopyranosyl-3¦Â-hydroxyolean-12-en-28-oic acid-28-O-¦Â-D-xylopyranoside
C46H76O16     ÏàËÆ¶È:57.1%
Indian Journal of Chemistry          2002          41B          884-886
Triterpenoid glycoside from Calotropis procera
Aditi Gupta, Anjali Gupta, Renu Rai, I R Siddiqui, J Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     3-O-[¦Á-L-rhamnopyranosyl( 1¡ú2)-¦Á-L-arabinopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl]-2¦Â-hydroxyoleanolic acid
C47H76O17     ÏàËÆ¶È:57.1%
Journal of Agricultural and Food Chemistry          2005          53          9954-9965
Triterpenoid Glycosides from Leaves of Medicago arborea L.
Aldo Tava, Mariella Mella, Pinarosa Avato, Maria Pia Argentieri, Zbigniew Bialy, and Marian Jurzysta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     Caryocaroside II-1
    ÏàËÆ¶È:55.5%
Journal of Natural Products          2006          69(2)          196-205
Triterpenoid Saponins from the Fruits of Caryocar glabrum
Abdulmagid Alabdul Magid, Laurence Voutquenne, Christian Moretti, Christophe Long, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     shishicrellastatin A
C56H83Na3O16S3     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2011          19          6594-6598
Shishicrellastatins, inhibitors of cathepsin B, from the marine sponge Crella (Yvesia) spinulata
Shuhei Murayama, Yasufumi Imae, Kentaro Takada, Jo Kikuchi, Yoichi Nakao, Rob W.M. van Soest, Shigeru Okada, Shigeki Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     compound 1
C47H74O18     ÏàËÆ¶È:55.1%
Phytochemistry          2006          67          2392-2397
Bioactive flavonoids and saponins from Climacoptera obtusifolia
Balakyz Yeskaliyeva, M. Ahmed Mesaik, Ahmed Abbaskhan, Aisha Kulsoom,G. Sh. Burasheva, Zh. A. Abilov, M. Iqbal Choudhary, Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     3-sulfate ester of 3¦Â,23-dihydroxyolean-12-en-28-oic acid 28-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C48H78O21S     ÏàËÆ¶È:55.1%
Journal of Natural Products          2008          71(6)          1000-1004
Antiproliferative Oleanane Saponins from Meryta denhamii
Giuseppina Cioffi, Fabrizio Dal Piaz, Antonio Vassallo, Fabio Venturella,Paolo De Caprariis, Francesco De Simone, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-Dgalactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,16¦Â,22¦Á-trihydroxy-olean-12-ene
C48H78O18     ÏàËÆ¶È:55.1%
Journal of Natural Products          2007          70          979-983
Oleanane Saponins from Stylosanthes erecta
Marinella De Leo,Rokia Sanogo, Nunziatina De Tommasi, and Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     3-¦Â-O-[¦Á-L-rhamnopyranosyl(1-3)-¦Â-glucuronopyranosyl]-2¦Â,3¦Â,dihydroxyolean-12-en-28-oic acid-28-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:55.1%
Phytochemistry          1998          49          195-198
Triterpenoid saponins from the seeds of amaranthus cruentus
MARTA JUNKUSZEW,WIESLAW OLESZEK MARIAN JURZYST¦Á,SONIA PIANCHENTE,COSIMO PIZZA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     3-O-¦Â-D-glucopyranosyl-3-¦Â-hydroxyolean-12-en-28-oic acid 28-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl] ester
C48H78O17     ÏàËÆ¶È:55.1%
Journal of Natural Products          2010          73          247-251
Sesquiterpene Lactones from Anthemis melanolepis and Their Antibacterial and Cytotoxic Activities. Prediction of Their Pharmacokinetic Profile
Vasiliki Saroglou, Anastasia Karioti, Ana Rancic, Kostas Dimas, Catherine Koukoulitsa, Maria Zervou and Helen Skaltsa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     Nebrosteroid J
C28H44O3     ÏàËÆ¶È:56.2%
Steroids          2009          74          543-547
New 19-oxygenated and 4-methylated steroids from the Formosan soft coral Nephthea chabroli
Shi-Yie Cheng, Ya-Chiang Huang, Zhi-Hong Wen, Chi-HsinHsu, Shang-Kwei Wang, Chang-Feng Dai, Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3,17-Bis(N,N-(1-Methoxycarbonyl-butan-1,4-diyl)-carboxamido)-carboxamido-androst-3,5,16-triene
C33H44O6N2     ÏàËÆ¶È:56.2%
Steroids          2011          76          280-290
Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation
P¨¦ter Ács, Attila Tak¨¢cs, Merc¨¦desz Kiss, No¨¦mi P¨¢link¨¢s, S¨¢ndor Mah¨®, L¨¢szl¨® Koll¨¢r
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     5-O-methylwithaphysalin R
C30H42O7     ÏàËÆ¶È:53.1%
Helvetica Chimica Acta          2007          Vol. 90          1406
Cytotoxic Withaphysalins from Physalis minima
Lei Ma, Xian-Wen Gan, Qing-Ping He, Hai-Yun Bai, Mohammad Arfan, Feng-Chang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     ananosic acid B
C32H48O4     ÏàËÆ¶È:53.1%
Journal of Natural Products          2004          67          875-877
Ananosic Acids B and C, Two New 18(13¡ú12)-abeo-Lanostane Triterpenoids from Kadsura ananosma
Ye-Gao Chen, Li-Na Hai, Xin-Rong Liao, Guo-Wei Qin, Yu-Yuan Xie, and Fathi Halaweish
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     5¦Á-ethoxy-6¦Â,14¦Á,17¦Â,20-tetrahydroxy-1-oxo-20S,22R-with a-2,24-dienolide
     ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          1993          41          1873-1875
Physapruins A and B, Two New Withanolides from Physalis pruinosa BAILEY
Kazushi SHINGU,Mariko MIYAGAWA,Shoji YAHARA and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     methyl fern-7-en-28-oate
C31H50O2     ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          1989          37          1673-1675
FERN CONSTITUENTS : THREE FERNENOIC ACIDS AND ONE ADIANENOIC ACID ISOLATED FROM RHIZOMES OF MICROSORIUM BRACHYLEPIS AND M. NORMALE
Kazuo MASUDA,Rumiko KAMAYA,Susumu IKEGAMI,Yukio IKESHIMA and Hiroyuki AGETA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     1 ',4 ',16,17-Tetrahydro-3¦Â-acetoxy-1' -acetyl-6' -methoxy-4' -methyl-(16¦Â,17¦Á)-androsta-5,16-dieno[17,16-b]quinoline
C32H43NO4     ÏàËÆ¶È:53.1%
Steroids          2004          69          301-312
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions
Ang¨¦la Magyar, J¨¢nos Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Me(24E)-3,4-secodammara-4(28),20,24-triene-26-oic acid-3-oate
C31H48O4     ÏàËÆ¶È:53.1%
Phytochemistry          1988          27          2915-2920
Six novel secodammarane-type triterpenes from male Flowers of Alnus japonica
Tadashi Aoki,Shinji Ohta,Takayuki Suga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 2
C30H46O4     ÏàËÆ¶È:53.1%
Phytochemistry          1988          27          2915-2920
Six novel secodammarane-type triterpenes from male Flowers of Alnus japonica
Tadashi Aoki,Shinji Ohta,Takayuki Suga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     compound 17
C32H50O4     ÏàËÆ¶È:53.1%
Phytochemistry          1988          27          2915-2920
Six novel secodammarane-type triterpenes from male Flowers of Alnus japonica
Tadashi Aoki,Shinji Ohta,Takayuki Suga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     20(R),24(E)-6¦Â-acetoxy-3-oxo-9¦Â-lanosta-7,24-dien-26-oic acid
    ÏàËÆ¶È:53.1%
Phytochemistry          1990          29          1629-1632
Lanost-7-en triterpenes from stem bark of Santiria trimera
M.F¨¢tima Das G.F. Da Silva,Regina H.P. Francisco,Alexander I. Gray,Johannes R. Lechat,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     methyl (4aS,8aS)-1,3,4,5,6,8a-hexahydro-2,2,7-trimethyl-8-{(2E)-2-[(4aS,8aS)-octahydro-5,5,8a-trimethyl-2-methylidenenaphthalen-1(2H)-ylidene]ethyl}naphthalene-4a(2H)-carboxylate
C31H48O2     ÏàËÆ¶È:53.1%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     24-ethyl-5¦Á-cholesta-7,trans-22,25(27)-trien-3¦Â-ol
    ÏàËÆ¶È:53.1%
Phytochemistry          1981          20          761-764
Co-occurrence of chondrillasterol and spinasterol in two cucurbitaceae seeds as shown by 13C NMR
Toshihiro Itoh, Yoshinori Kikuchi, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5¦Á-ethoxy-1-oxo-6¦Â-14¦Á,17¦Â,20¦Á-tetrahydroxy-20S,22R-with a-2,24-dienolide
C30H44O8     ÏàËÆ¶È:53.1%
Phytochemistry          1981          20          1359-1364
New withanolides of biogenetic interest from Withania somnifera
Vincent Vande Velde, David Lavie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     2¦Á,25-dimethylmeli-anodiol-[(21R,23R)-epoxy-24-hydroxyl-21¦Á,25-methoxy] tirucalla-7-en-3-one
    ÏàËÆ¶È:53.1%
Chinese Journal of Natural Medicines          2009          7          31-33
Triterpenes from the Fruits of Phellodendron chinense Schneid var. glabriusculum Schneid
YAN Chen; WANG Ye; HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 4''
    ÏàËÆ¶È:53.1%
Chemistry of Natural Compounds          2010          46          33-35
Synthesis oftertiaryamidomethyl derivatives of 2-isobornyl-4-methylphenol
E. V. Buravlev, I. Yu. Chukicheva and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (12R,20S)-12,20-dihydroxy-24-methylene-3,4-secodammar-4(28)-en-3-oci acid
C31H52O4     ÏàËÆ¶È:53.1%
Bulletin of the Chemical Society of Japan          1979          52          1698-1700
Structure of Alnustic Acid, a New Secodammarane-type Triterpenic Acid from Alnus sieboldiana
Takayuki Suga, Tadashi Aoki, Toshifumi Hirata, Keiko Aoki (n¨¦e Sukemiya), Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (22E)-3¦Â-Acetoxy-5¦Á-bromo-6,19-epoxystigmast-22-ene
C31H49BrO2     ÏàËÆ¶È:53.1%
Tetrahedron          2012          68          3685-3691
Synthesis of aromatic stigmastanes: application to the synthesis of aromatic analogs of brassinosteroids
Sof¨ªa L. Acebedo, Fernando Alonso, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     6-Methyl 2-[(1R,2S,5R)-5-Methyl-2-(2-phenylpropan-2-yl)cyclohexyl](2R)-2-(3,4-Dimethylpent-3-en-1-yl)-1,2-dihydroquinoline-2,6-dicarboxylate
C35H45NO4     ÏàËÆ¶È:53.1%
European Journal of Organic Chemistry          2012                   975-987
Enantioselective Annulation Reactions of Bisenolates Prepared Through Dearomatization Reactions of Aromatic and Heteroaromatic Diesters
Jaime P¨¦rez-V¨¢zquez, Alberte X. Veiga, Gustavo Prado, F. Javier Sardina and M. Rita Paleo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (3b,24R)-3-(acetyloxy)eupha-7,25-dien-24-ol
C32H52O3     ÏàËÆ¶È:53.1%
Helvetica Chimica Acta          2011          94          2061-2065
Euphane Triterpenes from the Bark of Broussonetia papyrifera (pages 2061¨C2065)
Han-Ting Zhong, Fu Li, Bin Chen and Ming-Kui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




21 .     24-(E)-3-oxodammara-20(21),24-dien-27-oic acid
C30H46O3     ÏàËÆ¶È:53.1%
Chemistry of Natural Compounds          2011          47          735-737
A new diarylheptanoid and a rare dammarane triterpenoid from Alnus nepalensis
Minh Giang Phan, Thi To Chinh Truong, Tong Son Phan, Katsuyoshi Matsunami and Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (24S)-24-isopropenyl-29-nor-5¦Á-lanosta-7-en-3¦Â-ol
C32H54O     ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung C          2003          58          649-654
Two New 24-Isopropenyl-lanostanoids from Tillandsia brachycaulos
Z. Cantillo-Ciau, G. J. Mena-Rej¨®n, E. Quintero-M¨¢rmol, A. Jim¨¦nez-D¨ªaz, and L. Quijano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




23 .     compound 9eaa
C88H104N4O8     ÏàËÆ¶È:53.1%
Tetrahedron          2012          68          6323-6328
Synthesis of upper rim N-formamido and isocyanocalix[4]arenes: adaptation of Ugi-4-CR on calix[4]arenes towards peptide-like architectures
Anupriya Savithri, Sreeja Thulasi, Luxmi Varma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (3¦Á,5¦Á)-3-Hydroxy-3-({4-[3-(trifluoromethyl)benzyl]-piperazin-1-yl}methyl)androstan-17-one
C32H45F3N2O2     ÏàËÆ¶È:53.1%
Bioorganic & Medicinal Chemistry          2011          19          4652-4668
Development of 3-substituted-androsterone derivatives as potent inhibitors of 17¦Â-hydroxysteroid dehydrogenase type 3
Ren¨¦ Maltais, Michelle-Audrey Fournier, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




25 .     Acetyl methyl sebiferenate
C35H54O6     ÏàËÆ¶È:52.9%
Phytochemistry          1984          23          2593-2595
Triterpenoid acids from Sapium sebiferum
Bhim P. Pradhan, Sibabrata De, Amer Nath, James N. Shoolery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     methyl (1R,12RS,15S,20S)-10-(1-methoxycar-bonyl-2-phenylethyl)-16,20-dimethyl-7-oxa-10-aza-tetracyclo[15.4.0.0(4,8).0(1,12)]eicosa-4(8),5-diene-16-carboxylate
C32H43NO5     ÏàËÆ¶È:52.7%
Russian Journal of Organic Chemistry          2005          41          535-545
Synthetic Transformations of Higher Terpenoids: IX. Nitrogen-Containing Heterocyclic Compounds on the Basis of Lambertianic Acid
S. V. Chernov, E. E. Shul¡¯ts, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




27 .     poriferasta-5,25-diene-3¦Â,4¦Â-diyl diacetate
C33H52O4     ÏàËÆ¶È:51.5%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     (E)-(25R)-23-acetyl-12-oxo-5¦Á-furosat-22-ene-3¦Â,26-diyl diacetate
C33H48O7     ÏàËÆ¶È:51.5%
Steroids          2010          75          1127-1136
Novel steroidal penta- and hexacyclic compounds derived from 12-oxospirostan sapogenins
Jos¨¦ Oscar H. P¨¦rez-D¨ªaz, Jos¨¦ Luis Vega-Baez, Jes¨²s Sandoval-Ram¨ªrez, Socorro Meza-Reyes, Sara Montiel-Smith, Norberto Farf¨¢n, Rosa Santillan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




29 .     compound 7
    ÏàËÆ¶È:51.5%
Tetrahedron Letters          2003          44          6673-6677
Degradation of triterpenic compounds from olive-pressing residues. Synthesis of trans-decalin type chiral synthons
Andr¨¦s Garcı́a-Granados, Pilar E L¨®pez, Enrique Melguizo, Andr¨¦s Parra, Yolanda Sime¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     (22E)-3¦Â,19-Diacetoxystigmasta-5,22-diene
C33H52O4     ÏàËÆ¶È:51.5%
Tetrahedron          2012          68          3685-3691
Synthesis of aromatic stigmastanes: application to the synthesis of aromatic analogs of brassinosteroids
Sof¨ªa L. Acebedo, Fernando Alonso, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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    ÏàËÆ¶È:61.2%
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1 .     Nebrosteroid J
C28H44O3     ÏàËÆ¶È:56.2%
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