| ²é¿´: 396 | »Ø¸´: 2 | ||
Àî½ð½Üͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú¸÷λ£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎï1:167.760,165.601,136.407,130.758,130.758,129.677,129.677,128.526,81.310,63.272,37.509,32.351,18.886,15.551¡£ »¯ºÏÎï2:199.521,164.392,156.102,135.015,134.023,132.550,124.479,124.435,123.013,55.714,44.343,44.004,42.884,39.293,36.774,35.607,34.137,33.099£¬29.709,27.726,15.380¡£ |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸085502£¬267·ÖÇóµ÷¼Á
ÒѾÓÐ16È˻ظ´
085801µçÆø×¨Ë¶272Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
366Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ37È˻ظ´
279ѧ˶ʳƷרҵÇóµ÷¼ÁԺУ
ÒѾÓÐ18È˻ظ´
290µ÷¼ÁÉúÎï0860
ÒѾÓÐ31È˻ظ´
Ò»Ö¾Ô¸085802 323·ÖÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
322Çóµ÷¼Á£¬08¹¤¿Æ
ÒѾÓÐ4È˻ظ´
²ÄÁϹ¤³Ì281»¹Óе÷¼Á»ú»áÂð
ÒѾÓÐ30È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú±ê×¼ÈÜÒºÅäÖÆ·½·¨
ÒѾÓÐ11È˻ظ´
ÇóÖú£¬Ð»Ð»¸÷λÀ²
ÒѾÓÐ1È˻ظ´
ÇóÖú°¡ ÑÎËáµÄÒì±û´¼ÈÜÒºÅäÖÆÒÔ¼°±ê¶¨£¬ÇóÖú¸÷λ£¬Ð»Ð»
ÒѾÓÐ11È˻ظ´
²»ÖªÔõô°ìÁË£¬ÇóÖú½â´ð£¬Ð»Ð»
ÒѾÓÐ6È˻ظ´
ÇóÖú°¡£¡ÓÐÈËÓÃsilvacoÖеÄatlasÄ£Äâ¹ýÌ«ÑôÄÜµç³ØÃ´£¿¼±Çó³ÌÐò£¬Ð»Ð»¸÷λ£¡
ÒѾÓÐ32È˻ظ´
ÇóÖú±¡²ã֪ʶ лл¸÷λ£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú£¡ºÜ¼±£¬Ð»Ð»¸÷λ
ÒѾÓÐ4È˻ظ´
ÓйØoriginÖеÄһЩÎÊÌ⣬·Ö¶ÈÖµµÄÎÊÌ⣬ÇóÖ¸µ¼£¬Ð»Ð»¸÷λ
ÒѾÓÐ8È˻ظ´
´óÈýÁË£¬¶ÔδÀ´ºÜÃÔ㣬Ï뿼ÑУ¬µ«²»ÖªµÀ·½Ïò£¬ÇóÖú¸÷λ£¡Ð»Ð»£¡£¡
ÒѾÓÐ32È˻ظ´
ÐÂÊÖmatlabÇóÖú£¬Ð»Ð»¸÷λ
ÒѾÓÐ10È˻ظ´
ÇóÖúJAVAÎÊÌ⣬лл¸÷λ´óÅ££¡
ÒѾÓÐ7È˻ظ´
¹ØÓÚ¼ÓÑù»ØÊÕÂʵÄÎÊÌ⣬ÓÐһʲ»½â£¬ÇóÖú¸÷λ£¬Ð»Ð»
ÒѾÓÐ8È˻ظ´
vasp¸Õ¿ªÊ¼°´¾Í³öÎÊÌâ¡¡ÇóÖú¸÷λ°¡
ÒѾÓÐ6È˻ظ´
ͶEA±»¾Ü£¨ÀíÓÉÏê¼ûÏ£©ÇóÍÆ¼öÏà¹ØÔÓÖ¾£¬Ð»Ð»¸÷λÁË
ÒѾÓÐ8È˻ظ´
ÇóÖú¸÷룬ÇëÎÊ´ó¼Ò·ÃѧÖ÷ҪѡѧУ»¹ÊÇרҵ£¿µ¼Ê¦¶¼²î²»¶àµÄÇé¿öÏÂ
ÒѾÓÐ7È˻ظ´
½ô¼±ÇóÖú¸÷λͯЬ£¬¹ØÓÚËÄäåË«·ÓAÈܽâÎÊÌ⣬лл´ó¼Ò£¡£¡
ÒѾÓÐ7È˻ظ´
ÇóÖú¸÷λ´óÏÀÒ»¸öÈ¥ôÇ»ù»¯µÄÎÊÌ⣬лл£¡
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿02-TPD±íÕ÷ÎÊÌ⣬лл¸÷λ´óÏÀ
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿Ð¡cc±»¾Ü£¬Çë¸÷Î»ÍÆ¼öÒ»ÏÂÆäËû¿ÉͶµÄÔÓÖ¾£¬Ð»Ð»
ÒѾÓÐ42È˻ظ´
¡¾ÇóÖú¡¿ÐÂÊÖ×ÔѧGIS,ÆÈÇÐÐèÒª°ïÖú,лл¸÷λÇ×°¡!ÓÐÖØ½ð¡¤¡¤¡¤¡¤¡¤¡¤
ÒѾÓÐ27È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿¹ØÓÚϸ¾ú¼ÆÊýµÈ£¬Ð»Ð»¸÷λ´óÅ£²ÎÓëÌÖÂÛ!
ÒѾÓÐ14È˻ظ´
¡¾ÇóÖú¡¿ÁªÏµÁË3¸öµ¼Ê¦¶¼µÃµ½»Ø¸´£¬Çë¸÷λ°ïæ·ÖÎöһϣ¬²¢Ö¸µãÔõô»Ø¸´£¬Ð»Ð»£¡
ÒѾÓÐ28È˻ظ´
¡¾ÇóÖú¡¿ÏëÎʸ÷λ¼«»¯ÇúÏßµÄÎÊÌ⣬лл
ÒѾÓÐ17È˻ظ´
¡¾ÇóÖú¡¿Ð¡µÜ£¬³õ´ÎʹÓó¬ÂËÀëÐĹܣ¬ÓÐÎÊÌâÇë½Ì¸÷λ´óÏÀ£¬Ð»Ð»¡£¡£
ÒѾÓÐ8È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Àî½ð½Ü(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-05-08 18:53:51
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Àî½ð½Ü(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-05-08 18:53:51
|
1 . bassiatin C15H19NO3 ÏàËÆ¶È:78.5% The Journal of Antibiotics 1995 48 1407-1412 Bassiatin, a New Platelet Aggregation Inhibitor Produced by Beauveria bassiana K-717 TERUMI KAGAMIZONO, EMIKO NISHINO, KEITA MATSUMOTO, AKIRA KAWASHIMA, MARI KISHIMOTO, NORIYOSHI SAKAI, BI-MEI HE, ZENG-XIANG CHEN, TAKASHI ADACHI, SHIGEO MORIMOTO, KAZUNORI HANADA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3R,6S)-4-methyl-6-(1-methylethyl)-3-phenylmethyl-1,4-perhydrooxazine-2,5-dione ÏàËÆ¶È:78.5% The Journal of Antibiotics 1995 48 1407-1412 Bassiatin, a New Platelet Aggregation Inhibitor Produced by Beauveria bassiana K-717 TERUMI KAGAMIZONO, EMIKO NISHINO, KEITA MATSUMOTO, AKIRA KAWASHIMA, MARI KISHIMOTO, NORIYOSHI SAKAI, BI-MEI HE, ZENG-XIANG CHEN, TAKASHI ADACHI, SHIGEO MORIMOTO, KAZUNORI HANADA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3S)-6-benzyl-3-isopropyl-1-methylperazine-2,5-dione C15H20N2O2 ÏàËÆ¶È:78.5% Chemical Journal of Chinese Universities 2014 35 1665-1669 Novel Diketopiperazine and Tenmembered Macrolides from the Entomogenous Fungus Paecilomyces tenuipes ZHENG Yong-biao, PANG Hai-yue, WANG Ji-feng, CHEN Dan-xia,SHI Guo-wei, HUANG Jian-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cyclo(l-6-Hyp-L-Phe) ÏàËÆ¶È:71.4% Journal of Natural Products 2006 69 580-584 Metabolites from the Marine-Derived Fungus Chromocleista sp. Isolated from a Deep-Water Sediment Sample Collected in the Gulf of Mexico Young Chul Park, Sarath P. Gunasekera, Jose V. Lopez, Peter J. McCarthy, and Amy E. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 6a ÏàËÆ¶È:62.5% Tetrahedron Letters 2004 45 3459-3463 Pyridazine derivatives. Part 38: Efficient Heck alkenylation at position 5 of the 6-phenyl-3(2H)-pyridazinone system Alberto Coelho, Eddy Sotelo, H¨¦ctor Novoa, Oswald M. Peeters, Norbert Blaton, Enrique Raviña Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . nortropane-3¦Á-7¦Â-diol 7-benzoate 3-(2¡ä-methylpropanoate) C18H23NO4 ÏàËÆ¶È:60% Heterocycles 2003 60 917-924 Nortropane Alkaloids from the Leaves of Erythoxylum moonii Khanzadi Fatima Khattak,* Atta-ur-Rahman, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-Methyl-4-[methyl(phenyl)amino]-4-oxobutyl Benzoate ÏàËÆ¶È:60% Helvetica Chimica Acta 2011 94 28-37 Reactions with 4-Hydroxy-2-methylbutananilides: Unexpected Formation of a Cyclopropanecarboxamide Maged K. G. Mekhael, Anthony Linden and Heinz Heimgartner Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Horizontoate A C15H20O4 ÏàËÆ¶È:60% Phytochemistry Letters 2014 10 204-208 Horizontoates A¨CC: New cholinesterase inhibitors from Cotoneaster horizontalis Shafiullah Khan, Zhao Wang, Runguo Wang, Liqun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl 4'-((2-(dimethylcarbamoyl)-2H-tetrazol-5-yl)methyl)biphenyl-3-carboxylate C19H19N5O3 ÏàËÆ¶È:58.8% European Journal of Medicinal Chemistry 2013 63 118-132 Biaryl tetrazolyl ureas as inhibitors of endocannabinoid metabolism: Modulation at the N-portion and distal phenyl ring Giorgio Ortar, Enrico Morera, Luciano De Petrocellis, Alessia Ligresti, Aniello Schiano Moriello, Ludovica Morera, Marianna Nalli, Rino Ragno,Adele Pirolli, Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 5 ÏàËÆ¶È:57.1% Natural Product Research 1997 11 13-16 Diketopiperazines from Cultures of the Fungus Colletotrichum gloesporoides Angel Trigos; Silvia Reyna; Ma. Luisa Gutierrez; Monica Sanchez Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Ethyl 5H-benzo[a]cycloheptene-7-carboxylate C14H14O2 ÏàËÆ¶È:57.1% Canadian Journal of Chemistry 2005 83 227-235 Substituent effects of the cycloaddition reaction of 7-substituted 5H-benzocycloheptenes with singlet oxygen and the chemistry of the benzocycloheptene endoperoxides Murat G¨¹ney, Zeynep Çelik Ceylan, Arif Da tan, and Metin Balci Structure 13C NMR ̼Æ×Ä£Äâͼ 222 |

2Â¥2015-03-11 15:30:41
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
|
222 1 . (S)-2-(2-(6-methoxy-2,3-dihydro-1H-inden-1-yl)ethyl)isoindoline-1,3-dione ÏàËÆ¶È:57.8% Heterocycles 2012 85 73-84 Stereoselective Synthesis of Melatonin Receptor Agonist Ramelteon via Asymmetric Michael Addition Xuan Zhang, Wei Yuan, Yu Luo, Qing-Qing Huang, and Wei Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 12 ÏàËÆ¶È:57.8% Chinese Chemical Letters 2011 22 264-267 Synthesis of the key intermediate of ramelteon Shan Bao Yu, Hao Min Liu, Yu Luo, Wei Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 10-Methyl-cis-¦Á-irone ÏàËÆ¶È:57.8% Helvetica Chimica Acta 1989 72 1400-1415 New Irone-Related Constituents from the essential oil of Iris germanica L. Bruno Maurer, Arnold Hauser and Jean-Claude Froidevaux Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (8¦Á,9¦Â,13¦Á,14¦Â,17¦Á)-2-(1,1-Dimethylethyl)estra-1,3,5(10)-trien-3,17-diol C22H32O2 ÏàËÆ¶È:55% Steroids 2007 72 351-359 A facile total synthesis of ent-17¦Â-estradiol and structurally related analogues Zu Yun Cai, Douglas F. Covey Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 19-nortestosterone ÏàËÆ¶È:52.6% Steroids 2005 70 193-198 Steroids¡¯ transformations in Penicillium notatum culture Agnieszka Bartma¨½ska, Jadwiga Dmochowska-Gładysz, Ewa Huszcza Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-[(4,4-Difluorocyclohexyl)carbonyl]-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinolin-4-one C19H22F2N2O2 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry Letters 2010 20 2481-2484 Praziquantel analogs with activity against juvenile Schistosoma mansoni Yuxiang Dong, Jacques Chollet, Mireille Vargas, Nuha R. Mansour, Quentin Bickle, Yazen Alnouti, Jiangeng Huang, Jennifer Keiser, Jonathan L. Vennerstrom Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â,17¦Â-dihydroxyandrost-4-ene ÏàËÆ¶È:52.6% Steroids 1999 64 770-779 Steroid transformations with Exophiala jeanselmei var. lecanii-corni and Ceratocystis paradoxa Roy B. R. Porter, Winklet A. Gallimore, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 5 C18H28O2 ÏàËÆ¶È:52.6% Tetrahedron Letters 1996 37 1241-1244 Chemistry of larixol I- degradation of the side-chain and microbial hydroxylation Denyse Herlem, Jamal Ouazzani, Françoise Khuong-Huu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . favelone C19H22O3 ÏàËÆ¶È:52.6% Tetrahedron 1994 50 5659-5668 Absolute stereochemistry of benzocycloheptenone derivatives from Cnidoscolus phyllacanthus Tomihisa Ohta, Yuichi Endo, Rikako Kikuchi, Chizuko Kabuto, Nobuyuki Harada, Shigeo Nozoe Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ethyl [4'H-spiro[adamantane-2,3'-isoquinolin]-1'(2'H)-ylidene]acetate C22H27NO2 ÏàËÆ¶È:52.6% Russian Journal of Organic Chemistry 2009 45 1874-1876 Synthesisof4¡äH-spiro[adamantane-2,3¡ä-isoquinoline]derivatives Yu. S. Rozhkova, O. A. Maiorova and Yu. V. Shklyaev Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2015-03-11 15:37:41













»Ø¸´´ËÂ¥