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ë®´ú¼×´¼£¬²é²»µ½£¬ÆäËüÈܼÁ²éµ½13¸ö£º²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . andibenin-B ÏàËÆ¶È:56% Journal of the Chemical Society, Perkin Transactions 1 1979 2118-2121 Studies on fungal metabolites. Part 1. The structures of andibenins-A and -C, and andilesins-A, -B, and -C, meroterpenoids from Aspergillus variecolor Thomas J. Simpson Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 57 ÏàËÆ¶È:54.1% Magnetic Resonance in Chemistry 1989 27 1166-1175 13C NMR data for isopimarane and 8-epi-isopimarane diterpenoids A. San Feliciano, M. Medarde, F. Tom¨¦, B. Hebrero and E. Caballero Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . glaucocalyxin B ÏàËÆ¶È:54.1% Chinese Tladitional Patent Medicine 2009 31 763-765 Chemical constituents from Rabdosia japonica var£®glaucocalyx XIANG Zhao-bao, XU Yi-xinl, CHEN Hai-sheng, HUANG Min-zhul Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . yesodine C25H35NO4 ÏàËÆ¶È:52% Heterocycles 1990 31 1081-1088 Studies on Aconitum Species. XIII. Two New Diterpenoid Alkaloids from Aconitum yesonese var. Macroyesoense (Nakai) Tamura. VI. Koji Wada, Hideo Bando, and Norio Kawahara Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 8 ÏàËÆ¶È:50% Journal of Natural Products 2000 63 226-229 Grindelane Diterpenoids from Stevia subpubescens Luisa U. Rom¨¢n, Jairo I. Cambr¨®n, Rosa E. del R¨ªo, Juan D. Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas, and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . caesalpinilinn C21H26O5 ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 121-123 Five New Cassane-Type Diterpenes from Caesalpinia crista Zheng-Yi Yang, Yin-Hua Yin, Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gyrosanol A C20H32O ÏàËÆ¶È:50% Journal of Natural Products 2010 73 1184-1187 Antiviral and Anti-inflammatory Diterpenoids from the Soft Coral Sinularia gyrosa Shi-Yie Cheng, Cheng-Ta Chuang, Shang-Kwei Wang, Zhi-Hong Wen, Shu-Fen Chiou, Chi-Hsin Hsu, Chang-Feng Dai and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-14-Methoxybutorphanol C22H31NO2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2808-2816 Synthesis and binding affinity of novel mono- and bivalent morphinan ligands for §Ü,¦Ì and ¦Ä opioid receptors Bin Zhang, Tangzhi Zhang, Anna W. Sromek, Thomas Scrimale, Jean M. Bidlack, John L. Neumeyer Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . preaustinoid A3 C26H32O7 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2007 62b 1035-1044 Four Additional Meroterpenes Produced by Penicillium sp Found in Association with Melia azedarach. Possible Biosynthetic Intermediates to Austin Taicia Pacheco Fill, Grace Kelli Pereira, Regina M. Geris dos Santos, and Edson Rodrigues-Fo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . phanginin N C21H26O6 ÏàËÆ¶È:50% Journal of China Pharmaceutical University 2012 43 209-210 A new cassane furanoditerpenoid from the seeds of Caesalpinia sappan ZHANG Jing-yu, QU Wei, LIANG Jing-yu* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . cattienoid B C22H28O3 ÏàËÆ¶È:50% Fitoterapia 2013 91 125-127 Cattienoids A¨CC, three novel steroids from the mushroom Tomophagus cattienensis Bui Thi Thu Hien, Le Thi Phuong Hoa, Le Xuan Tham, Dang Ngoc Quang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Daphmacromine L C22H29NO4 ÏàËÆ¶È:50% Fitoterapia 2013 89 205-209 Daphmacromines K¨CO, alkaloids from Daphniphyllum macropodum Ming-Ming Cao, Lei Wang, Yu Zhang, Hong-Ping He, Yu-Cheng Gu, Qiang Zhang, Yan Li, Chun-Mao Yuan, Shun-Lin Li, Ying-Tong Di, Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 37 C26H38O5 ÏàËÆ¶È:50% Tetrahedron 2014 70 3030-3041 Efficient transformation of 7,14-dihydroxy-ent-kaurenes to novel ent-abietanes having cis-fused ¦Á-methylene ¦Ã-lactones under Mitsunobu reaction conditions and their cytotoxicities Yutaka Aoyagi, Kei Ozawa, Tatsuya Kobayashi, Tomoyo Hasuda, Ming-Yu Gui, Yong-Ri Jin, Xu-Wen Li, Haruhiko Fukaya, Reiko Yano, Yukio Hitotsuyanagi, Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ |

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