| ²é¿´: 217 | »Ø¸´: 1 | ||
IMB001½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
| ̼Æ×Êý¾ÝÈçÏ£º14.8, 22.4, 28.7, 31.8, 36.8, 39.2, 40.3, 41.1, 43.1, 59.2, 82.8, 93.3, 130.5, 144.7. |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
audreygc
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 236 (´óѧÉú)
- ½ð±Ò: 5115.1
- ºì»¨: 5
- Ìû×Ó: 519
- ÔÚÏß: 131Сʱ
- ³æºÅ: 1978000
- ×¢²á: 2012-09-05
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
IMB001: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-20 17:40:08
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
IMB001: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-20 17:40:08
|
²éѯ½á¹û£º¹²²éµ½183¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . conicumol ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2000 48(8) 1190-1195 Ichthyotoxic Phloroglucinol Derivatives from Dryopteris fragrans and Their Anti-tumor Promoting Activity Hideyuki ITO,Takashi MURANAKA,Kazuko MORI,Zhe-Xiong JIN,Harukuni TOKUDA,Hoyoku NISHINO and Takashi YOSHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . presilphiperfolan-1-ol ÏàËÆ¶È:60% Phytochemistry 1999 51 517-523 Sesquiterpenes from the essential oil of the liverwort Conocephalum conicum Stephanie Melching, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . eujavanoic acid B C14H22O3 ÏàËÆ¶È:57.1% Journal of Natural Products 2004 67 1580-1583 New Decalin Derivatives, Eujavanoic Acids A and B, from Eupenicillium javanicum Shigeru Okamoto, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Kaoru Okada, Galba Maria de Campos Takaki, Minoru Chikamori, Takashi Yaguchi, Kazutaka Fukushima, Makoto Miyaji, and Ken-ichi Kawai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 6 C28H38O4 ÏàËÆ¶È:57.1% Tetrahedron Letters 2000 41 2831-2834 Copper(I)-catalyzed intramolecular photocycloadditions of dicyclopentadiene derivatives linked by removable tethers Ravikrishna Chebolu, Wei Zhang, Elena Galoppini, Richard Gilardi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (¡À)-4a,7-epoxy-1,2,3,4,7,8,9a-heptahydro-4,4,7¦Á,9a¦Â-tetramethyl-4aH-benzocyclohepten-9(¦Á)-ol C15C24O2 ÏàËÆ¶È:57.1% Heterocycles 2004 62 583-618 Intramolecular [4+3] Cycloadditions. Towards a Synthesis of Widdrol Michael Harmata,* Mehmet Kahraman, Gilbert Adenu, and Charles L. Barnes Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . rac-3-Butyloctahydro-1H-4,7-methanoinden-1-one C14H22O ÏàËÆ¶È:57.1% Zeitschrift f¨¹r Naturforschung B 2006 61 589-596 Synthesis of Pentalene Systems Employing a Sequence of Pauson-Khand Reaction, Michael Reaction, and Desilylation A. Becheanu, T. Bell, S. Laschat, A. Baro, W. Frey, N. Steinke, and P. Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (¡À)-cis-2-(2-butyloxy-cyclopent-3-enyl)-ethanol C12H23O2 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2010 18 2920-2929 Synthesis and biological activity of conformationally restricted gypsy moth pheromone mimics Hao Chen, Yongmei Gong, Regine M. Gries, Erika Plettner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-ethynyl-2-(1-hydroxypentyl)cyclohex-2-en-1-one ÏàËÆ¶È:57.1% Heterocycles 2012 84 983-1012 Synthesis of 8-Hydroxyisochromenes and 8-Hydroxyisocoumarins from 3-Ethoxycyclohex-2-en-1-one George Majetich* and Jeremy L. Grove Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . N-(4-formylbenzyl)octanamide ÏàËÆ¶È:57.1% Journal of Medicinal Chemistry 2010 53 4849-4861 Amphiphilic Amide Nitrones: A New Class of Protective Agents Acting as Modifiers of Mitochondrial Metabolism Grégory Durand, Burkhard Poeggeler, Stéphanie Ortial, Ange Polidori, Frederick A. Villamena, Jutta Böker, Rüdiger Hardeland, Miguel A. Pappolla and Bernard Pucci Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . pulchranin A C14H29N3O ÏàËÆ¶È:57.1% Tetrahedron Letters 2013 54 1247-1250 Pulchranin A, isolated from the Far-Eastern marine sponge, Monanchora pulchra: the first marine non-peptide inhibitor of TRPV-1 channels Alla G. Guzii, Tatyana N. Makarieva, Yuliya V. Korolkova, Yaroslav A. Andreev, Irina V. Mosharova, Ksenya M. Tabakmaher, Vladimir A. Denisenko, Pavel S. Dmitrenok, Ekaterina K. Ogurtsova, Alexandr S. Antonov, Hyi-Seung Lee, Eugene V. Grishin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1-acetoxy-3,5-dibutyladamantane C20H34O2 ÏàËÆ¶È:57.1% Tetrahedron 2013 69 3238-3248 Synthesis and ring-opening reaction of novel 1,3-dehydroadamantanes possessing phenyl and alkoxyl substituents Sotaro Inomata, Yusuke Harada, Shin-ichi Matsuoka, Takashi Ishizone Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (4R,2'S)-4-(2'-Hydroxyheptyl)-1,5-diazocan-2-one C13H26N2O2 ÏàËÆ¶È:57.1% The Journal of Organic Chemistry 2012 77 9724-9737 Absolute Configuration Assignment by Asymmetric Syntheses of the Homalium Alkaloids (− -(R,R,R)-Hoprominol and (− -(4¡äS,4¡åR,2‴R)-HopromalinolStephen G. Davies, James A. Lee, Paul M. Roberts, Jeffrey P. Stonehouse, and James E. Thomson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 3 ÏàËÆ¶È:56.2% Phytochemistry 1996 42 771-774 A tetranorfriedolabdane diterpene from Vellozia stipitata Ângelo C. Pinto, Octavio A. C. Antunes, Moacir G. Pizzolatti, Victor M. Rumjanek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . compound 7 ÏàËÆ¶È:56.2% Phytochemistry 1996 42 771-774 A tetranorfriedolabdane diterpene from Vellozia stipitata Ângelo C. Pinto, Octavio A. C. Antunes, Moacir G. Pizzolatti, Victor M. Rumjanek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 5(6)-Tetranorfriedolabden-12-oic acid C16H26O2 ÏàËÆ¶È:56.2% Phytochemistry 1995 38 1269-1271 Minor cleisthantane and tetranorfriedolabdane from Vellozia flavicans Angelo C. Pinto, Oct¨¢vio A. C. Antunes, Claudia M. Rezende, Carlos Roque D. Correia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 5(6)-Tetranorfriedolabden-12-ol C16H28O ÏàËÆ¶È:56.2% Phytochemistry 1995 38 1269-1271 Minor cleisthantane and tetranorfriedolabdane from Vellozia flavicans Angelo C. Pinto, Oct¨¢vio A. C. Antunes, Claudia M. Rezende, Carlos Roque D. Correia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . tert-butyl (2S,4S)-4-butyl-4-hydroxy-1-p-toluenesulfonylpyrrolidine-2-carboxylate C18H27NO5S ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2009 57 167-176 Conversion of 4-Oxoproline Esters to 4-Substituted Pyrrole-2-carboxylic Acid Esters Yasushi Arakawa, Naomi Yagi, Yukimi Arakawa, Ken-ichi Tanaka and Shigeyuki Yoshifuji Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . tert-butyl (2S,4R)-4-ethoxycarbonylmethyl-4-hydroxy-1-p-toluenesulfonylpyrrolidine-2-carboxylate C20H29NO7S ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2009 57 167-176 Conversion of 4-Oxoproline Esters to 4-Substituted Pyrrole-2-carboxylic Acid Esters Yasushi Arakawa, Naomi Yagi, Yukimi Arakawa, Ken-ichi Tanaka and Shigeyuki Yoshifuji Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . cadinane-4¦Â,5¦Á,10¦Â-triol C15H28O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . axinysone E C15H20O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(12) 2004-2010 Sesquiterpenes from the Sponge Axinyssa isabela Eva Zub¨ªa, Mar¨ªa J. Ortega, and J. Luis Carballo Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-06-20 15:33:12














»Ø¸´´ËÂ¥
-(R,R,R)-Hoprominol and (−