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schaduwÎÞ³æ (СÓÐÃûÆø)
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ë®´úÂÈ·Â CÆ× 12.44, 14.14, 22.10, 22.70, 25.95, 29.37, 29.71, 31.93, 33.64, 36.25, 37.12, 37.33, 37.47, 40.67, 46.78, 48.31, 48.82, 50.44, 52.60, 54.37, 54.71, 56.00, 59.34, 78.45, 79.94, 84.78, 118.89, 137.25, 218.51 |
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1 . Hemsleyaconitine G C24H37NO4 ÏàËÆ¶È:82.7% Helvetica Chimica Acta 2011 94 268-272 Hemsleyaconitines F and G, Two Novel C19-Diterpenoid Alkaloids Possessing a Unique Skeleton from Aconitum hemsleyanum Yong Shen, Ai-Xue Zuo, Zhi-Yong Jiang, Xue-Mei Zhang, Hong-Ling Wang and Ji-Jun Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2,2-dinitrobetulone ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 2012 48 821-826 Preparation and nitration of allobetulin seco-derivatives A. V. Shernyukov , I. Ya. Mainagashev, D. V. Korchagina, Yu. V. Gatilov, N. F. Salakhutdinov, G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . acoforine ÏàËÆ¶È:62.0% China Journal of Chinese Materia Medica 2009 34 1927-1929 Diterpenoidalk aloids from Aconitum handelianum YANG Jin, LIU Wei, YANG Xiaodong, ZHAO Jingfeng, LIU Fu, LILiang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 7 ÏàËÆ¶È:62.0% Journal of Natural Products 1992 Vol 55 767 Starfish Saponins, Part 47. Steroidal Glycoside Sulfates and Polyhydroxysteroids from Aphelasterias japonica E. Finamore, F. Zollo, L. Minale, Takeshi Yasumoto Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (24R)-stigmast-7,22(E)-dien-3-ol ÏàËÆ¶È:62.0% Chinese Pharmaceutical Journal 2010 45 1460-1462 Chemical Components in Championella sarcorrhiza DONG Jian-yong, TIAN Li-li, LIN Chen, YUE Lei, ZHANG Yuan, LIN Guan-yang, CAI Jin-zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . delphatine ÏàËÆ¶È:62.0% Pharmaceutical Biology 2006 44 244-246 Alkaloids from Consolida olopetala. L. Bitiş, S. S¨¹zgeç, F. Meriçli, H. Özçelik, J. Zapp, H. Becker, A.H. Meriçli Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . acoforine C28H45NO6 ÏàËÆ¶È:62.0% Heterocycles 1987 25 365-376 The Structures of Four New C19-Diterpenoid Alkaloids from Aconitum forrestii Stapf S. William Pelletier, Balawant S. Joshi, Jan A. Glinski, Hitesh P. Chokshi, Szu-ying Chen, Krishna Bhandary, and Kuantee Go Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3,20-Dioxo-29-nor-lupan-28-oic acid ÏàËÆ¶È:62.0% Natural Product Communications 2008 3 1569-1574 Oxidative Decarboxylation of Triterpene C-28 Acids ofLupane Series Nataliya G. §¬omissarova, Nataliya G. Belenkova, Olga V. Shitikova, Leonid V. Spirikhin andMarat S. Yunusov Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Fruticoside B C29H46O4 ÏàËÆ¶È:62.0% Journal of Natural Products 2011 74 1161-1168 Triterpene and Sterol Derivatives from the Roots of Breynia fruticosa Ya-Ping Liu, Xiang-Hai Cai, Tao Feng, Yan Li, Xiao-Ning Li, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . donellanic acid A C29H42O4 ÏàËÆ¶È:62.0% Tetrahedron 2012 68 4621-4627 Donellanic acids A¨CC: new cyclopropanic oleanane derivatives from Donella ubanguiensis (Sapotaceae) Aurelie V.B. Djoumessi, Louis P. Sandjo, Johannes C. Liermann, Dieter Schollmeyer, Victor Kuete, Vincent Rincheval, Abegaz M. Berhanu, Samuel O. Yeboah, Pascal Wafo, Bonaventure T. Ngadjui, Till Opatz Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . methyl 3-oxolupan-28-oate C31H50O3 ÏàËÆ¶È:61.2% Russian Journal of Organic Chemistry 2009 45 1464-1467 First examples of hydroxycyclopropanation in the series of lupane triterpenoids V. N. Odinokov, E. R. Shakurova, L. M. Khalilov and U. M. Dzhemilev Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . methyl 1-isopropenyl-5b,8,8,12a-tetramethyl-2,3,3a,4,5,5a,5b,6,7,7,a,8,12,12a,12b,13,14,14a,14b-octadecahydro-1H-cyclopenta[7,8]chryseno[2,3-d][1,2,3]thiadiazole-3a-carboxylate C31H46N2O2S ÏàËÆ¶È:61.2% Russian Journal of Organic Chemistry 2004 40 90-92 Synthesis of 1,2,3-Thiadiazolo Terpenoids on the Basis of Cyclopentanonopimaric and Betulonic Acids O. B. Flekhter, E. V. Tret'yakova, N. I. Medvedeva, L. A. Baltinax and F. Z. Galin, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . schleicheol 1 C30H52O2 ÏàËÆ¶È:60% Journal of Natural Products 2000 63 72-78 Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1 George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Betulinic acid ÏàËÆ¶È:60% Archives of Pharmacal Research 2011 Vol 34,No 7 1097-1105 Constituents of the Root of Anemone tomentosa Hao-Bin Hu, Xu-Dong Zheng, Yu-Feng Jian, Jian-Xin Liu, and Ji-Hua Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . betulinic acid ÏàËÆ¶È:60% Chinese Pharmaceutical Journal 2011 46 252-255 Study on Chemical Constituents of the Root of Anemone tomentosa HU Hao-bin, ZHENG Xu-dong, ZHU Ji-hua, LI Yan, ZHANG Xiao-wei Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . kongboendine C32H43NO7 ÏàËÆ¶È:60% Natural Product Research and Development 2002 14(5) 6-8 STRUCTURE OF KONGBOENDINE APing; CHEN Dong lin; CHEN Qiao hong; JIAN Xi xian; WANG Feng peng Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . pteroxygonumnol A C30H46O4 ÏàËÆ¶È:60% Helvetica Chimica Acta 2012 95 127-133 A New Triterpene and Phenolic Compounds from the Roots of Pteroxygonum giraldii Xin Chai, Yan-Fang Su, Jun Zhang, Shi-Lun Yan, Yan-Hong Gao and Xiu-Mei Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . acetylation of bacosine ÏàËÆ¶È:60% Indian Journal of Chemistry Section B 2000 39B 620-625 Bacosterol, a new 13,14-seco-steroid and bacosine, a new triterpene from Bacopa monniera Bahar Ahmad & A Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Betulinic Acid ÏàËÆ¶È:60% Chemistry of Natural Compounds 2012 48 870-872 Chemical Constituents of the Stem Bark of Acanthopanax brachypus from China Hu Haobin, Zheng Xudong, Li Yan Structure 13C NMR ̼Æ×Ä£Äâͼ |

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