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²éѯ½á¹û£º¹²²éµ½143¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . artesteversin C30H36O5 ÏàËÆ¶È:60% Phytochemistry 1985 24 1009-1015 Dimeric guaianolides from Artemisia sieversiana Ferdinand Bohlmann, Widayati Ang, Carola Trinks, Jasmin Jakupovic, Siegfried Huneck Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Allosxde A ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 1991 27 198-207 STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES FROM PLANTS OF THE GENUS Allium. XXVII. ALLIOSTEROL AND ALLOSIDES A AND B FROM Allium suvorovii AND Allium stipitatum - STRUCTURAL ANALOGS OF FUROSTANOLS Yu. S. Vollerner, S. D Kravets,A. S. Shashkov, B. Tashkhodzhaev,M. B. Gorovits, M. R. Yagudaev,and N. K. Abubakirov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-(hydroxymethyl)-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,-17-dioxabicyclo[11.3.1]heptadecane-3,10-dione ÏàËÆ¶È:54.5% Journal of the American Chemical Society 2000 122 619-631 Stereocontrolled Elaboration of Natural (− -Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudaiLeo A. Paquette, Louis Barriault, Dmitri Pissarnitski, and Jeffrey N. Johnston Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Antifungalmycin C35H60O14 ÏàËÆ¶È:54.2% Natural Products and Bioprospecting 2012 2 41-45 Antifungalmycin, an antifungal macrolide from Streptomyces padanus 702 Yi-Fen Wang, Sai-Jin Wei, Zhi-Ping Zhang, Tong-He Zhan, Guo-Quan Tu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Pseudolarolide O C30H42O5 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2003 Vol. 86 787 Pseudolarolides O and P, Two Novel Triterpene Dilactones from Pseudolarix kaempferi Guo-Fu Chen, Chang-Heng Tan, Zhu-Lian Li, Shan-Hao Jiang, and Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . neviotine b C30H50O6 ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 175-180 New Triterpenoids from the Red Sea Sponge Siphonochalina siphonella Yoel Kashman, Tesfamariam Yosief, and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3¦Á,5¦Á,19¦Â,28-diepoxy-A-neo-18¦Á-oleane C30H48O2 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2006 42 618-619 STRUCTURE OF THE MINOR OZONOLYSIS PRODUCT OF 19b,28-EPOXY-A-neo-18a-OLEAN-3(5)-ENE N. I. Medvedeva, O. B. Flekhter,A. Gzella, and L. Zaprutko Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 19¦Â,28-Epoxy-18¦Á-olean-3(5)-ene C30H48O ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2004 40 247-249 SYNTHESIS OF 4,5-SECO-DERIVATIVES OF ALLOBETULIN N. I. Medvedeva, O. B. Flekhter, L. A. Baltina,F. Z. Galin, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 11 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 1984 20 170-173 GLYCOSYLATION OF BETULIN AND ITS ACETATES IN THE PRESENCE OF CADMIUM CARBONATE L. E. Odinokova, G. I. Oshitok, V. A. Denisenko, V. F. Anufriev, A. M, Tolkach, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . pseudolarohde K C30H44O7 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 1999 2 207-214 Structures and Stereochemistry of Pseudolarolides K and L, Novel Triterpene Dilactones from Pseudolarix Kaempferi KE CHEN, QIAN SHI, ZHU-LIAN LI, CHI-DUEN POONC, REN-JIU TANG and KUO-HSIUNG LEE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . herniaria saponin A C65H102O32 ÏàËÆ¶È:53.3% Natural Product Research 1995 6 233-240 Herniaria Saponin A, A Novel Saponin from Herniaria Fontanesii Addi Nait Mbark; Zoubida Charrouf; Jean Michel Wieruszeski; Yves Leroy; Ossarath Kol Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . acnistin E ÏàËÆ¶È:53.3% Phytochemistry 1994 36 1297-1301 Acnistins C and D, withanolides from Dunalia solanacea Javier G. Luis, Fernando Echeverri, Antonio G. Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 93 ÏàËÆ¶È:53.3% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Ainsliadimer C C30H36O7 ÏàËÆ¶È:53.3% Planta Medica 2011 77 1545-1550 New Sesquiterpenoids from Ainsliaea macrocephala and Their Nitric Oxide Inhibitory Activity Zhi-JunWu, Xi-Ke Xu, Hua-Wu Zeng, Yun-Heng Shen, Jun-Mian Tian, Juan Su, Hui-Liang Li, Lei Shan, Run-Hui Liu, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 19¦Â,28-Epoxy-A-neo-18¦Á-olean-3(5)-ene C30H48O ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 579-582 ALLYLIC OXIDATION OF 19¦Â,28-EPOXY-A-NEO-5 -METHYL-25-NOR-18¦Á-OLEAN-9-ENE O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov,N. I. Medvedeva, and L. V. Spirikhin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Anthogorgsteroid D C26H44O4 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2012 95 522-527 Polyhydroxylated Steroids from the South China Sea Gorgonian Anthogorgia Peng Sun,Yuanyuan Xu,Taofang Liu,Hua Tang,Yanghua Yi, Karsten Krohn,Ling Li, and Wen Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:53.3% Chinese Traditional and Herbal Drugs 2010 41 1065-1068 СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿ Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . A-Nor-5¦ÁH-19¦Â,28-epoxy-18¦Á-olean-3(5)-ene C30H48O ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2004 40 1092-1097 Synthetic Transformations of Higher Terpenoids: XI. Synthesis of A-Nor-5bH-19b,28-epoxy-18a-olean-3-one Derivatives N. I. Medvedeva, O. B. Flekhter, E. V. Tretyakova, F. Z. Galin and L. A. Baltina, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |
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-Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudai