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yang09529: ½ð±Ò+10, ¡ïÓаïÖú 2013-10-21 09:55:28
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yang09529: ½ð±Ò+10, ¡ïÓаïÖú 2013-10-21 09:55:28
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½18¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 5 C14H18O5 ÏàËÆ¶È:52.9% Heterocycles 2010 82 491-504 Asymmetric Syntheses of Highly Functionalized Bicyclo[2.2.2]octene Derivatives Masafumi Iwatsu, Daisuke Urabe, and Masayuki Inoue Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4,5-Dideoxy-2,3-O-isopropylidene-4-N-tosylamino-L-arabinosediethylacetal C19H31NO6SCs ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 1994 2 1179-1188 Five-membered ring azasugars as potent inhibitors of ¦Á-L-rhamnosidase (naringinase) from Penicillium decumbens Louis Provencher, Darryl H. Steensma, Chi-Huey Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-(3'-Azido-3'-deoxy-¦Â-D-ribofuranosyl) nicotinamide 5'-(butyl phosphate) C15H22N5O7P ÏàËÆ¶È:52.9% Heterocycles 2011 83 2837-2850 Studies on the Synthesis of Nicotinamide Nucleoside and Nucleotide Analogues and Their Inhibitions towards CD38 NADase Zhe Chen, Anna Ka Yee Kwong, Zhenjun Yang, Liangren Zhang,* Hon Cheung Lee, and Lihe Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 15 C18H32O2 ÏàËÆ¶È:52.9% Australian Journal of Chemistry 2009 62 676-682 Formal Total Synthesis of (+)-Citrafungin A Sammi Tsegay, Helmut H¨¹gel and Mark A. Rizzacasa Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (2R*,4S*,6S*)-2-methyl-6-(4-oxoheptyl)-4-(phenylsulfonyl)piperidine C19H29NO3S ÏàËÆ¶È:52.9% Tetrahedron 2013 69 1499-1508 Synthetic studies of quinolizidine 195C and derivatives Shang-Shing P. Chou, Jun-Wei Zhang, Kuan-Hua Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Decurrenside E C19H24O8 ÏàËÆ¶È:52.9% Journal of Natural Products 2012 75 88-92 Benzyl Benzoate Glycoside and 3-Deoxy-d-manno-2-octulosonic Acid Derivatives from Solidago decurrens Ken Shiraiwa, Shen Yuan, Ayako Fujiyama, Yosuke Matsuo, Takashi Tanaka, Zhi-Hong Jiang, and Isao Kouno Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound 6b ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry Letters 1997 7 2125-2130 Synthesis and evaluation of benzophenone-based photoaffinity labeling analogs of prenyl pyrophosphates containing stable amide linkages Tammy C. Turek, Igor Gaon, Dave Gamache, Mark D. Distefano Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . sulfate A C26H41O7S ÏàËÆ¶È:50% Journal of Natural Products 1998 61 1374-1378 Acanthosterol Sulfates A-J: Ten New Antifungal Steroidal Sulfates from a Marine Sponge Acanthodendrilla sp. Sachiko Tsukamoto, Shigeki Matsunaga, Nobuhiro Fusetani, and Rob W. M. van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . atis-16-en-14-oxo-13(S),3¦Â-diol C20H30O3 ÏàËÆ¶È:50% Chinese Chemical Letters 1990 1 13-16 FIVE NEW DITERPENES FROM EUPHORBIA SIEBOLDIANA YI LI DING ZHONG JIAN JIA AND YU TING LIU Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . lonicerine ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 2166 Indole Alkaloids from Kopsia teoi T. Varea, C. Kan, F. Remy, T. Sevenet, J. C. Quirion, H.-P. Husson, H. A. Hadi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ent-3¦Â,(13S)-dihydroxyatis-16-en-14-one C20H30O3 ÏàËÆ¶È:50% Phytochemistry 1990 29 1925-1935 Ent-atisane diterpenes from Euphorbia fidjiana Allick R. Lal,Richard C. Cambie,Peter S. Rutledge,Paul D. Woodgate Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ent-13R,3¦Â-dihydroxy-14-oxo-atis-16-ene C20H30O3 ÏàËÆ¶È:50% Phytochemistry 1990 29 2343-2345 Two diterpenes from Euphorbia sieboldiana Zhong-Jian Jia,Yi-Li Ding,Qi-Guang Wang,Yu-Ting Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . wulingzhic acid A C20H32O5 ÏàËÆ¶È:50% Fitoterapia 2010 81 381-384 Two new isopimarane diterpenes from the feces of Trogopterus xanthipes Nian-Yun Yang, Wei-Wei Tao, Min Zhu, Jin-Ao Duan, Jian-Guo Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ent-3¦Â,(13S)-Dihydroxyatis-16-en-14-one C20H30O3 ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2004 35 611-613 Diterpenoids from Euphorbia wallichii WANG Huan; ZHANG Xiao-feng; MA Yun-bao; CAI Xiang-hai; WU Da-gang; LUO Xiao-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . neriifolene ÏàËÆ¶È:50% Chinese Journal of Natural Medicines 2010 8 101-103 Diterpenes and Triterpenes from the Roots of Euphorbia fischeriana WU Qi-Cheng; TANG Yu-Ping; DING An-Wei; YOU Fen-Qiang; DUAN Jin-Ao Structure 13C NMR ̼Æ×Ä£Äâͼ |

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