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qinpei8901: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-16 22:23:46
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qinpei8901: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-16 22:23:46
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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£º¹²²éµ½24¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (1R*,2E,4R*,7E,10S*,11S*,12R*)-10,18-diacetoxydolabella-2,7-dien-6-one C24H36O5 ÏàËÆ¶È:58.3% Journal of Natural Products 1998 61 1096-1100 Three Dolabellanes and a Macrolide from the Sponge Dysidea sp. from Palau Qing Lu and D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 8-Deepoxyangeloyl-8-[2-hydroxy-3-chloro-isobutyroyl]enhydrin ÏàËÆ¶È:54.1% Phytochemistry 1995 38 433-435 2¦Á, 3¦Â-dihydroxy-4(18)-neo-cleroden-15-oic acid from cistus populifolius Julio G. Urones, Isidro S. Marcos, Pilar Basabe, Alicia Jimenez, Antonio Gomez, Anna M. Lithgow Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 20¦Á-Acetylamino-11¦Á-hydroxy-5¦Á-pregnan-3-on ÏàËÆ¶È:54.1% Steroids 1998 63 484-495 Microbial hydroxylation of acetylaminosteroids HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . khayanone C27H34O9 ÏàËÆ¶È:51.8% Journal of Natural Products 2001 64 1107-1110 Antifeedant Rings B and D Opened Limonoids from Khaya senegalensis Munehiro Nakatani,Samir A. M. Abdelgaleil,Junichi Kurawaki, Hiroaki Okamura,Tetsuo Iwagawa, and Matsumi Doe Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . khayanone ÏàËÆ¶È:51.8% Natural Product Research 2008 22 763-800 13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family T. Narender; T. Khaliq; Shweta Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 6 C27H42N4O7 ÏàËÆ¶È:51.8% Tetrahedron Letters 2005 46 1483-1487 An efficient entry to new sugar modified ketolide antibiotics Alex Romero, Chang-Hsing Liang, Yu-Hung Chiu, Sulan Yao, Jonathan Duffield, Steven J. Sucheck, Ken Marby, David Rabuka, Po Yee Leung, Youe-Kong Shue, Yoshi Ichikawa, Chan-Kou Hwang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . longistylumphylline A C23H29NO3 ÏàËÆ¶È:50% Helvetica Chimica Acta 2005 Vol. 88 854 Longistylumphyllines A-C, Three New Alkaloids from Daphniphyllum longistylum Xin Chen, Zha-Jun Zhan, Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . terretonin A C26H32O8 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 1243-1246 Sesterterpenoids, Terretonins A−D, and an Alkaloid, Asterrelenin, from Aspergillus terreus Guo-You Li, Bo-Gang Li, Tao Yang, Jian-Hua Yin, Hua-Yi Qi, Guang-Ye Liu, and Guo-Lin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . decahydrotabersonine ÏàËÆ¶È:50% Journal of Natural Products 1997 60 419-420 Perhydrogenation of Tabersonine, an Aspidosperma Indole Alkaloid Guy Lewin, Corinne Schaeffer, and Catherine Dacquet Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Daphlongamine F C23H29NO4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 653-659 Alkaloids from the Leaves of Daphniphyllum lo |

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