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361810541½ð³æ (СÓÐÃûÆø)
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[ÇóÖú]
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| 13C NMR (101 MHz, CDCl3) ¦Ä16.08, 19.23,21.19, 26.17, 27.54, 29.06, 30.26, 34.89, 35.75, 38.51, 43.43, 52.25, 53.33, 56.66, 62.80, 75.97, 77.23, 82.98, 99.42, 127.27, 129.02, 135.57, 136.41 ,170.61,175.78,204.29 |
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361810541: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-04 17:51:07
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°´´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£º¹²²éµ½347¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . berkeleyacetal A C26H32O8 ÏàËÆ¶È:80.7% Journal of Natural Products 2007 70 1820-1823 The Berkeleyacetals, Three Meroterpenes from a Deep Water Acid Mine Waste Penicillium Donald B. Stierle,Andrea A. Stierle, and Brianna Patacini Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . epoxycytochalasin H ÏàËÆ¶È:60.7% Journal of Agricultural and Food Chemistry 1982 30 301-304 Isolation and identification of two new [11]cytochalasins from Phomopsis sojae Richard J. Cole, David M. Wilson, James L. Harper, Richard H. Cox, Teena W. Cochran, Horace G. Cutler, Durham K. Bell Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (2S,4aR,6aR,7R,9S,10aS,10bR)-Methyl 9-acetoxy-6a,10bdimethyl-4,10-dioxo-2-((S)-1-((R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoyloxy)but-3-enyl)dodecahydro-1Hbenzo[f]isochromene-7-carboxylate ÏàËÆ¶È:58.0% Organic & Biomolecular Chemistry 2009 7 3748-3756 Synthetic studies of neoclerodane diterpenes from Salvia divinorum: role of the furan in affinity for opioid receptors Denise S. Simpson, Kimberly M. Lovell, Anthony Lozama, Nina Han, Victor W. Day, Christina M. Dersch, Richard B. Rothman and Thomas E. Prisinzano Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl 6¦Â,15-diacetoxy-7-labden-17-oate ÏàËÆ¶È:57.6% Phytochemistry 1989 28 557-560 Minor labdane diterpenoids from Halimium verticillatum Julio G. Urones,Isidro S. Marcos,David D. Martin,Maria C. Alonso Alonso,Fernando M.S. Brito Palma,Jesus M.L. Rodilla Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Emeriphenolicin B C24H34NO5Cl ÏàËÆ¶È:57.6% Phytochemistry 2011 72 1436-1442 Antiviral isoindolone derivatives from an endophytic fungus Emericella sp. associated with Aegiceras corniculatum Guojian Zhang, Shiwei Sun, Tianjiao Zhu, Zhenjian Lin, Jingyan Gu, Dehai Li ⇑, Qianqun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . deacetylepoxycytochalasin H ÏàËÆ¶È:57.6% Journal of Agricultural and Food Chemistry 1982 30 301-304 Isolation and identification of two new [11]cytochalasins from Phomopsis sojae Richard J. Cole, David M. Wilson, James L. Harper, Richard H. Cox, Teena W. Cochran, Horace G. Cutler, Durham K. Bell Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 1a C24H36O6 ÏàËÆ¶È:57.6% Magnetic Resonance in Chemistry 2012 50 709-712 Structure elucidation and NMR assignments of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice Ming-Tao Liu, Na Luan, Jin-Jie Li, Xiao Huang, Ye-Feng Wang, A-Li Wang and Xiao-Ya Shang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Methyl (E)-9-[(1S,2R,3R,5S)-2-(2-Acetoxyethyl)-3,5-bis(tert-butyldimethylsilyloxy)cyclopentyl]-7-(tert-butyldimethylsilyloxy)non-8-enoate C37H74O7Si3 ÏàËÆ¶È:57.1% European Journal of Organic Chemistry 2012 2621-2634 Total Synthesis of Isoprostanes Derived from Adrenic Acid and EPA Camille Oger, Val¨¦rie Bultel-Ponc¨¦, Alexandre Guy, Thierry Durand and Jean-Marie Galano Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 26b C26H37NO6 ÏàËÆ¶È:57.1% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6,12,13,14-Diepoxycytochalasin B C29H37NO7 ÏàËÆ¶È:55.5% Magnetic Resonance in Chemistry 2008 46 650-659 Synthesis, complete 1H and 13C NMR assignment and crystal structure of novel epoxide derivatives of cytochalasin B (pages 650¨C659) Pieter S. Steyn, Jaco C. Breytenbach, Jeanne H. Botha, Manuel A. Fernandes and Philippus L. Wessels Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 1 C56H80N2O14S4 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2009 17 7435-7440 Synthesis and biological evaluation of epothilone A dimeric compounds Daniele Passarella, Daniela Comi, Graziella Cappelletti, Daniele Cartelli, Juerg Gertsch, Ana R. Quesada, Jurgen Borlak, Karl-Heinz Altmann Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 13-acetoxy-20-O-angelylingenol C27H36O8 ÏàËÆ¶È:55.5% Chinese Chemical Letters 2011 22 451-454 Isolation and characterization of ingenol esters from Euphorbia cornigera Imam Bakhsh Baloch, Musa Kaleem Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 26ac C29H37NO7 ÏàËÆ¶È:55.5% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 27s C29H40N2O5 ÏàËÆ¶È:55.5% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . lobarialide C C29H42O3 ÏàËÆ¶È:55.1% Chemistry & Biodiversity 2009 6 746-752 Lobarialides A¨CC, Antifungal Triterpenoids from the Lichen Lobaria kurokawae Xiao-Ning Wang, Hai-Juan Zhang, Dong-Mei Ren, Mei Ji, Wen-Tao Yu, and Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 19 C42H57NO4Si ÏàËÆ¶È:55.1% Organic Letters 2004 Vol. 6, No. 12 2055-2058 Assignment of Absolute Stereochemistry and Total Synthesis of (-)-Spongidepsin Arun K. Ghosh and Xiaoming Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . N-Benzyl 3¦Á,7¦Á,24-trimethoxy-12-az¦Á-5¦Â-cholane C33H53NO3 ÏàËÆ¶È:54.8% Steroids 2011 76 324-330 Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols Malika Ibrahim-Ouali, Khalil Hamze, Luc Rocheblave Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . umbellacin D C23H36O7 ÏàËÆ¶È:53.8% Journal of Natural Products 2006 69 338-341 Cytotoxic Xenia Diterpenoids from the Soft Coral Xenia umbellata Ali A. H. El-Gamal, Shang-Kwei Wang, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . daphmanidin A ÏàËÆ¶È:53.8% Journal of Natural Products 2006 69 1065-1069 Daphnioldhanins A−C, Alkaloids from Daphniphyllum oldhami Shu-Zhen Mu, Ye Wang, Hong-Ping He, Xian-Wen Yang, Yue-Hu Wang, Ying-Tong Di, Yang Lu, Ying Chang, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ |

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