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²éѯ½á¹û£º¹²²éµ½49¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cyclo-(L-isoleucyl-L-prolyl-L-leucyl-L-prolyl) C22H36N4O4 ÏàËÆ¶È:58.3% Journal of Natural Products 2003 66 883-884 A New Cyclic Peptide from a Marine-Derived Bacterium of the Genus Nocardiopsis Jongheon Shin, Youngwan Seo, Hyi-Seung Lee,Jung-Rae Rho, and Sang Jun Mo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . barbilycopodin ÏàËÆ¶È:58.3% Journal of the Chemical Society, Perkin Transactions 1 1986 809-814 Dolabellane diterpenoids from the liverworts Barbilophozia floerkei, B. lycopodioides, and B. attenuata: spectroscopic and X-ray studies of structure, stereochemistry, and conformation. X-Ray molecular structure of 3S,4S;7S,8S-diepoxy-10R,18-dihydroxydoll Siegfried Huneck, George A. Baxter, A. Forbes Cameron, Joseph D. Connolly, Leslie J. Harrison, William R. Phillips, David S. Rycroft and George A. Sim Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . MKN-349A ÏàËÆ¶È:58.3% Helvetica Chimica Acta 2014 97 1564-1570 A New Cyclic Peptide and a New Steroid from the Fungus Penicillium sp. GD6 Isolated from the Mangrove Bruguiera gymnorrhiza Zhen-Fang Zhou, Xiao-Hong Yang, Hai-Li Liu, Yu-Cheng Gu, Bo-Ping Ye and Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . tenacibactin C C23H42N4O8 ÏàËÆ¶È:54.1% Journal of Natural Products 2007 70 563-566 Tenacibactins A-D, Hydroxamate Siderophores from a Marine-Derived Bacterium, Tenacibaculum sp. A4K-17 Jae-Hyuk Jang,Kaneo Kanoh, Kyoko Adachi, Satoru Matsuda, and Yoshikazu Shizuri Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (22R,23R)-3¦Â-Acetoxy-5¦Á,22,23-trihydroxystigmastan-6-one C31H52O6 ÏàËÆ¶È:54.1% Steroids 2000 65 329-337 Synthesis and bioactivity evaluation of brassinosteroid analogs Javier A. Ram¨ªrez, Osvaldo M. Teme Centuri¨®n, Eduardo G. Gros, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . teucrolin D C22H30O9 ÏàËÆ¶È:54.1% Journal of Natural Products 1993 Vol 56 830 Neocleordane Diterpenoids and Their Artifacts from Teucrium olivarianum Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly, Andrew T. McPhail Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 10R,18-diacetoxydolabella-3E,7E-diene C24H38O4 ÏàËÆ¶È:54.1% Journal of the Chemical Society, Perkin Transactions 1 1986 809-814 Dolabellane diterpenoids from the liverworts Barbilophozia floerkei, B. lycopodioides, and B. attenuata: spectroscopic and X-ray studies of structure, stereochemistry, and conformation. X-Ray molecular structure of 3S,4S;7S,8S-diepoxy-10R,18-dihydroxydoll Siegfried Huneck, George A. Baxter, A. Forbes Cameron, Joseph D. Connolly, Leslie J. Harrison, William R. Phillips, David S. Rycroft and George A. Sim Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â,8¦Á,9¦Â-triacetoxy-4¦Á-hydroxy-7-epi-eudesmane C21H34O7 ÏàËÆ¶È:54.1% The Journal of Organic Chemistry 2005 70 338-341 Enzyme-Catalyzed Rearrangement of a Diepoxy-germacrane Compound into New 7-epi-Eudesmane Derivatives Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Antonio Mart¨ªnez, and Francisco Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-(2-(acetyloxy)ethyl)-2,5,5,8a-tetramethyldecahydro-2-naphthalenyl acetate C22H36O6 ÏàËÆ¶È:54.1% Tetrahedron 2001 57 5663-5679 The synthesis of Ambrox®-like compounds starting from (+)-larixol Marjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-(2-(acetyloxy)ethyl)-2,5,5,8a-tetramethyldecahydro-2-naphthalenyl acetate C22H36O6 ÏàËÆ¶È:54.1% Tetrahedron 2001 57 8369-8379 The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2 Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 22-½µ-3¦Â-ÒÒõ£Ñõ»ù¶¹çÞ-6-ͪ-22-È© ÏàËÆ¶È:54.1% Chinese Journal of Organic Chemistry 2014 34 1816-1828 Synthesis and Antiproliferative Evaluation of Some Steroidal Oxime Ether Huang, Yanmin Su, Shaoyang Jia, Linyi Gan, Chunfang Lin, Qifu Kong, Erbin Cui, Jianguo Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-((3E)-5-(acetyloxy)-3-methyl-3-pentenyl)-2,5,5,8a-tetramethyl-decahydro-2-naphthalenyl acetate C24H38O4 ÏàËÆ¶È:53.8% Tetrahedron 2001 57 5663-5679 The synthesis of Ambrox®-like compounds starting from (+)-larixol Marjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-((3E)-5-(acetyloxy)-3-methyl-3-pentenyl)-2,5,5,8a-tetramethyl-decahydro-2-naphthalenyl acetate C24H38O4 ÏàËÆ¶È:53.8% Tetrahedron 2001 57 8369-8379 The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2 Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ent-18,3¦Â,7¦Á,17-Tetracetoxy-15¦Â,16bepoxykaurane 28H40O9 ÏàËÆ¶È:53.5% Phytochemistry 2005 66 1492-1498 ent-Kauranoid derivatives from Sideritis moorei Hanae Ghoumari, Mohamed-Hassan Benajiba, Amina Azmani,Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra,Francisco Rivas, Oswaldo Socorro Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . cyclo(L-Val-D-Ile-L-Leu-L-pro-D-Leu) C28H49N5O5 ÏàËÆ¶È:53.5% Journal of Natural Products 2011 74 1303-1308 Isolation and Structural Elucidation of Proline-Containing Cyclopentapeptides from an Endolichenic Xylaria sp. Wen Wu, Huanqin Dai, Li Bao, Biao Ren, Jingcai Lu, Yuanming Luo, Liangdong Guo, Lixin Zhang, and Hongwei Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 6¦Á-hydroxyhop-21¦ÂH-22(29)-en C30H50O ÏàËÆ¶È:52% Pharmaceutical Biology 2006 44 217-220 Chemistry and Bioactivity of Physciaceae Lichens Pyxine consocians. and Heterodermia leucomelos. Selvaluxmy Kathirgamanathar, W.D. Ratnasooriya, Peter Baekstrom, Raymond J. Andersen, Veranja Karunaratne Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . krempfielin J C23H38O5 ÏàËÆ¶È:52% Marine Drugs 2013 11 2741-2750 Krempfielins J-M, New Eunicellin-Based Diterpenoids from the Soft Coral Cladiella krempfi Yan-Ning Lee, Chi-Jen Tai, Tsong-Long Hwang and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Á-acetoxi-22(R),23-epoxi-24-nor-5¦Â-colan-12-ona C25H38O4 ÏàËÆ¶È:52% Journal of the Chilean Chemical Society 2002 47 511-516 SINTESIS Y ACTIVIDAD BIOLOGICA DE ANALOGOS DE BRASINOESTEROIDES LUIS ESPINOZA C Y MANUEL CORTES M* Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Á,11¦Á,20-Triacetoxy-1¦Â-iodo-5¦Â-pregnane C27H41IO6 ÏàËÆ¶È:51.8% Steroids 2011 76 1458-1464 Microwave assisted preparation of C(1)-C(11) oxygen-bridged pregnanes Lautaro D. Alvarez, Juan M. Sonego, Adriana S. Veleiro, Gerardo Burton Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 37 C29H48O3 ÏàËÆ¶È:51.7% Journal of the American Chemical Society 2010 132 5300-5308 Biomimetic Syntheses from Squalene-Like Precursors: Synthesis of ent-Abudinol B and Reassessment of the Structure of Muzitone Matthew A. Boone, Rongbiao Tong, Frank E. McDonald, Sheri Lense, Rui Cao and Kenneth I. Hardcastle Structure 13C NMR ̼Æ×Ä£Äâͼ |

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