| ²é¿´: 307 | »Ø¸´: 2 | ||
zhiwu1983ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
|
̼Æ×Êý¾ÝÈçÏ£º 221.8,170.1,169.8,143.3,139.8,123.0,110.7,78.5,71.3,70.4,61.2,43.2,43.0,42.7,41.3,40.9,40.2,38.5,37.8,36.8,36.5,28.6,27.5,24.9,22.2,21.7,21.5,20.3,17.1 |
» ²ÂÄãϲ»¶
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ26È˻ظ´
¿¼ÑжþÂÖµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϸ´ÊÔÇóµ÷¼Á
ÒѾÓÐ17È˻ظ´
085601³õÊÔ330·ÖÕÒµ÷¼Á
ÒѾÓÐ9È˻ظ´
291 Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ17È˻ظ´
0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ4È˻ظ´
²©Ê¿×Ô¼ö
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´

yaolan123
½û³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 183 (¸ßÖÐÉú)
- ¹ó±ö: 0.255
- ½ð±Ò: 15027.2
- É¢½ð: 2847
- ºì»¨: 173
- ɳ·¢: 3
- Ìû×Ó: 3217
- ÔÚÏß: 486.8Сʱ
- ³æºÅ: 1352788
- ×¢²á: 2011-07-21
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û

2Â¥2013-05-02 20:07:27
yaolan123
½û³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 183 (¸ßÖÐÉú)
- ¹ó±ö: 0.255
- ½ð±Ò: 15027.2
- É¢½ð: 2847
- ºì»¨: 173
- ɳ·¢: 3
- Ìû×Ó: 3217
- ÔÚÏß: 486.8Сʱ
- ³æºÅ: 1352788
- ×¢²á: 2011-07-21
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-05-02 20:43:28
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-05-02 20:43:28
|
1 . Mesendanin C C32H44O9 ÏàËÆ¶È:81.2% Journal of Natural Products 2010 73 1344-1349 Mesendanins A−J, Limonoids from the Leaves and Twigs of Melia toosendan Shi-Hui Dong, Chuan-Rui Zhang, Xiu-Feng He, Hong-Bing Liu, Yan Wu and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Mesendanin D C30H42O7 ÏàËÆ¶È:70% Journal of Natural Products 2010 73 1344-1349 Mesendanins A−J, Limonoids from the Leaves and Twigs of Melia toosendan Shi-Hui Dong, Chuan-Rui Zhang, Xiu-Feng He, Hong-Bing Liu, Yan Wu and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . hongdoushan A C29H44O7 ÏàËÆ¶È:65.5% Journal of Natural Products 2002 65 1700-1702 Three New C-14 Oxygenated Taxanes from the Wood of Taxus yunnanensis Arjun H. Banskota, Tepy Usia, Yasuhiro Tezuka, Kyoji Kouda, Nhan Trung Nguyen, and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 7-acetylneotrichilenone ÏàËÆ¶È:65.5% Phytochemistry 2000 55 711-713 A limonoid from Trichilia estipulata Di¨®genes A.G. Cortez, João B. Fernandes, Paulo C. Vieira, M. Fa tima das G.F da Silva, A. Gilberto Ferreira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 7-acetylneotrichilenone ÏàËÆ¶È:65.5% Phytochemistry 1998 49 2493-2496 Meliacin butenolides from Trichilia estipulata Di¨®genes A. G. Cortez, João B. Fernandes, Paulo C. Vieria, M. F¨¢tima das G. F. da Silva, Antonio G. Ferreira, Qu¨¦zia B. Cass, Jos¨¦ Rubens Pirani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Meliarachin A C28H40O8 ÏàËÆ¶È:65.5% Helvetica Chimica Acta 2011 Vol. 94 1515-1526 Meliarachins A¨CK: Eleven Limonoids from the Twigs and Leaves of Melia azedarach Zu-Shang Su, Sheng-Ping Yang, Sheng Zhang, Lei Dong, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 7-acetylneotrichilenone ÏàËÆ¶È:65.5% Phytochemistry 1981 20 117-120 Tetranortriterpenoids from the seeds of Azadirachta indica Wolfgang Kraus, Rudolf Cramer, Gisela Sawitzki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (22R,25S)-22-Hydroxyfurost-5-ene-3b,26-diyl diacetate C31H48O6 ÏàËÆ¶È:64.5% Steroids 2012 77 59-66 Rapid conversion of spirostans into furostan skeletons at room temperature Omar Viñas-Bravo, Roxana Martinez-Pascual, Jos¨¦ Luis Vega-Baez, V¨ªctor G¨®mez-Calvario, Jes¨²s Sandoval-Ram¨ªrez, Sara Montiel-Smith, Socorro Meza-Reyes, Alejandra L¨®pez-De Rosas, M¨®nica Mart¨ªnez-Montiel, Mayra Reyes, Jos¨¦ A. Ruiz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Meliatoosenin H C31H40O11 ÏàËÆ¶È:64.5% Phytochemistry 2012 73 106-113 Limonoids from the fruits of Melia toosendan Yi Zhang, Chun-Ping Tang, Chang-Qiang Ke, Xi-Qiang Li, Hua Xie, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Sorbinol A C30H46O3 ÏàËÆ¶È:63.3% Magnetic Resonance in Chemistry 2007 45 416-419 Isolation and structural determination of sorbinols A and B, new triterpenes from Sorbus cashmariana, by 1D and 2D NMR spectroscopy (pages 416¨C419) Mehdi Hassan Kazmi, Ejaz Ahmed, Saira Hameed, Abdul Malik and Muhammad Ashraf Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (20S)-3¦Â-acetoxy-20-hydroxyergosta-5,24(28)-diene C30H46O4 ÏàËÆ¶È:63.3% Australian Journal of Chemistry 1998 51 1157-1165 Four New Compounds from the Australian Brown Alga Cystophora brownii Baohong Bian and Ian A. van Altena Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 5¦Á-Ergosta-7,9(11),22-triene-3¦Â,5-diol 3-acetate C30H46O3 ÏàËÆ¶È:63.3% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . khivorin ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 14 . khivorin ÏàËÆ¶È:62.5% Journal of the Chemical Society, Perkin Transactions 1 1974 437-441 13 C nuclear magnetic resonance spectra of some limonoids. Part I. The structure of procerin, an extractive from Carapa procera David A. H. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (3¦Â,5¦Á)-20-hydroxy-6-oxocevan-3-yl acetate C29H45NO4 ÏàËÆ¶È:62.0% Chemistry & Biodiversity 2008 Vol. 5 259 Cytotoxic Alkaloids from the Bulbs of Fritillaria hupehensis Yong-Hui Zhang, Xi-Liang Yang, Peng Zhang, Xue-Feng Zhou, Han-Li Ruan, Hui-Fang Pi, Ji-Zhou Wu, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . massileunicellin C C26H38O8 ÏàËÆ¶È:62.0% Helvetica Chimica Acta 1999 Vol. 82 1681 A Novel Type of a Second Epoxy Bridge in Eunicellane Diterpenes: Isolation and Characterization of Massileunicellins A¡ÀC from the Gorgonian Eunicella cavolinii Ines Mancinia), Graziano Guellaa), Helmut Zibrowiusb), Dominique Laurentc), and Francesco Pietra Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 4'-O-acetyl-3-pregna-5,20-dienyl-¦Â-D-arabinopyranoside C28H42O6 ÏàËÆ¶È:62.0% Journal of Natural Products 2006 69 1379-1383 Antiplasmodial Metabolites Isolated from the Marine Octocoral Muricea austera Marcelino Gutirrez, Todd L. Capson, Hctor M. Guzmn, Jos Gonzlez, Eduardo Ortega-Barra, Emilio Quio, and Ricardo Riguera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . rabdoforrestin A C28H38O10 ÏàËÆ¶È:62.0% Acta Botanica Yunnanica 1996 18£¨2£© 234-238 Revision of the Structures of 7-acetyl-lushanrubescensin A,Rand of orrestin a,and related diterpenoids ZHAO Qin-Shi,LIN Zhong-Wen,SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 3¦Â,7¦Á,22-trihydoxystigmast-5-ene C29H50O3 ÏàËÆ¶È:62.0% Chinese Chemical Letters 2004 15 194-196 A New Stigmasterol and a New Eremophilenolide from Ligularia dolichobotrys Er Wei LI, Kun GAO, Zhong Jian JIA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 5,6¦Á-Dihydroxy-5¦Á-cholest-7-en-3¦Â-yl acetate C29H48O4 ÏàËÆ¶È:62.0% Steroids 2006 71 565-577 Regio and stereoselective oxidations of unsaturated steroidal compounds with H2O2 mediated by CH3ReO3 Francesco P. Ballistreri, Rosa Chillemi, Sebastiano Sciuto, Gaetano A. Tomaselli, Rosa M. Toscano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 12¦Á-acetoxyneotrichilinone C28H36O6 ÏàËÆ¶È:62.0% Phytochemistry 1998 49 2585-2590 Limonoids from Turraea holstii and Turraea floribunda Dulcie A. Mulholland, Thabo V. Monkhe, Philip H. Coombes, Mahomed S. Rajab Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . Forrestin D C28H40O10 ÏàËÆ¶È:62.0% Phytochemistry 1993 34 461-465 Diterpenoids from Rabdosia forrestii Yunlong Xu, Isao Kubo, Chungshih Tang, Fenglei Zhang, Handong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Cipadonoid A C29H38O10 ÏàËÆ¶È:62.0% Organic Letters 2008 Vol.10,No.10 1905-1908 Cipadonoid A, a Novel Limonoid with an Unprecedented Skeleton, from Cipadessa cinerasecns Xin Fang, Ying-Tong Di, Hong-Ping He, Hai-Yang Liu, Zhen Zhang,Yan-Li Ren, Zhu-Lin Gao,Suo Gao,and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . Toonayunnanin B C30H40O6 ÏàËÆ¶È:62.0% Phytochemistry 2012 76 141-149 Limonoids from the leaves of Toona ciliata var. yunnanensis Jie-Qing Liu,Cui-Fang Wang,Yan Li,Jian-Chao Chen,Lin Zhou,Ming-Hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 3¦Â,7¦Á,22-trihydroxy-stigmast-5-ene C29H50O3 ÏàËÆ¶È:62.0% Pharmazie 2004 59 646-649 Two new compounds from Ligularia dolichobotrys Er-Wei Li, Kun Gao, and Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 2¦Á,5¦Á,10¦Â-triacetoxy-14¦Â-(2'-methyl)-butyryloxy-4(20),11-taxadiene C31H46O8 ÏàËÆ¶È:61.2% Journal of Natural Products 1994 Vol 57 1320 Yunnanxane and Its Homologous Esters from Cell Cultures of Taxus chinensis var. mairei Wenwen Ma, Roy W. Stahlhut, Tom L. Adams, Gary L. Park, William A. Evans, Sibylle G. Blumenthal, George A. Gomez, Matthew H. Nieder, Peter J. Hylands Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . Meliarachin G C31H40O11 ÏàËÆ¶È:61.2% Helvetica Chimica Acta 2011 Vol. 94 1515-1526 Meliarachins A¨CK: Eleven Limonoids from the Twigs and Leaves of Melia azedarach Zu-Shang Su, Sheng-Ping Yang, Sheng Zhang, Lei Dong, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . Meliarachin K C31H40O11 ÏàËÆ¶È:61.2% Helvetica Chimica Acta 2011 Vol. 94 1515-1526 Meliarachins A¨CK: Eleven Limonoids from the Twigs and Leaves of Melia azedarach Zu-Shang Su, Sheng-Ping Yang, Sheng Zhang, Lei Dong, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . sinenxane C C31H46O8 ÏàËÆ¶È:61.2% Zeitschrift f¨¹r Naturforschung C 2007 62 1-10 Simultaneous Identification and Determination of Major Taxoids from Extracts of Taxus chinensis Cell Cultures C. F. Zhao, L. J. Yu, L. Q. Li, and F. Xiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . compound 6 ÏàËÆ¶È:61.2% Organic Magnetic Resonance 1983 21 524-525 Carbon-13 NMR spectra of ¦¤4(20).11- taxadiene derivatives Deanna De Marcano, Bernardo M¨¦ndez, Jeannette De M¨¦ndez, Jos¨¦ Monasterios, An¨ªbal C. Rojas and Thomas G. Halsall Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-05-02 20:13:53













»Ø¸´´ËÂ¥