| ²é¿´: 268 | »Ø¸´: 1 | ||
zhou_biaoľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÔÚÏߵȴý ΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
VIBe43 CÆ×Êý¾ÝÈçÏ£º 16.1,22.5,30.0,34.1,42.7,54.8,61.6,72.0,86.2,118.0,123.1,124.0,130.3 |
» ²ÂÄãϲ»¶
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´
»¯Ñ§070300 Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
»¯¹¤Ñ§Ë¶294·Ö£¬Çóµ¼Ê¦ÊÕÁô
ÒѾÓÐ12È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúJAKSTATµÄ·¢ÏÖÀúÊ·£¬¼±£¬ÔÚÏߵȣ¡
ÒѾÓÐ4È˻ظ´
ÇóÖú¹ú¼Ê»áÒéµÄ¸ñʽ£¬ÔÚÏßµÈ
ÒѾÓÐ8È˻ظ´
ÇóÖúÕâ¾ä»°µÄ¾äʽ½á¹¹·ÖÎö£¬ÔÚÏߵȣ¬¹ò°ÝÁË£¡
ÒѾÓÐ44È˻ظ´
ÇóÖúºìÍâÈí¼þOPUS£¬ÔÚÏߵȴýÖÐ
ÒѾÓÐ3È˻ظ´
¡¾ÔÚÏߵȡ¿ÇóÖú¸÷λ×ÊÉî³æÓÑ£¬3ƪÎÄÕµÈ×ÅÄã¡£¡£¡£
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚvbµ÷ÓÃdll£¬×ö³ÉexeºóÔÚ±ðÈ˵çÄÔÉÏÎÞ·¨ÔËÐУ¨ÔÚÏߵȣ©
ÒѾÓÐ14È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
Ͷcatalysis communicationsÇóÖú-ÔÚÏßµÈ
ÒѾÓÐ12È˻ظ´
ÐźŴ¦ÀíͶ¸åÇóÖú ÔÚÏßµÈ
ÒѾÓÐ3È˻ظ´
Ͷ¸åʱµÄСÎÊÌâ~ÇóÖú~ÔÚÏßµÈ~лл
ÒѾÓÐ8È˻ظ´
ÇóÖú£ºspringerͶ¸åÎÊÌ⣨ÔÚÏߵȣ©
ÒѾÓÐ7È˻ظ´
EQCMʹÓÃÇóÖú ½ô¼±ÇóÖú ÔÚÏßµÈ
ÒѾÓÐ11È˻ظ´
Journal of Chemical Sciences ÇóÖú
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿¼±Çóbeckman allegra X-15RÀä¶³ÀëÐÄ»ú²Ù×÷Êֲᡪ¡ªÔÚÏßµÈ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿°ï·ÖÎöÏÂ×ܵªµÄ±ê×¼ÇúÏßÊÇÔõô»ØÊ£¿¼±£¡ÔÚÏߵȣ¡
ÒѾÓÐ21È˻ظ´
¡¾ÇóÖú¡¿ÔÚÏߵȣ¬¹ØÓÚHÆ×ÓÃDMSOÖеÄË®·å
ÒѾÓÐ4È˻ظ´
½ô¼±ÇóÖú£¬ÔÚÏߵȸ÷λ´ïÈË£¬¿´¿´±à¼»Ø¸´µÄÕâ¾ä»°ÊÇʲôÒâ˼
ÒѾÓÐ14È˻ظ´
¡¾ÇóÖú¡¿µÍµçλϹ¤×÷µç¼«¡¢¶Ôµç¼«Ã°ÆøÅÝ ÔÚÏߵȴý
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿Í¶¸åÖм¸¸ö·Ò루ÔÚÏߵȣ©
ÒѾÓÐ5È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhou_biao: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-10 16:11:23
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhou_biao: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-10 16:11:23
|
1 . tyromol A ÏàËÆ¶È:60% Journal of Anhui Agricultural Sciences 2014 42 1578-1581 Two new sesquiterpenoids from basidiomycete Tyromyces chioneus GUO Hua, FENG Tao, LI Zheng-hui, LIU Ji-kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Compound 10 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2010 20 4206-4209 Synthesis of two marine farnesylacetones that dilate the basilar arteries of rabbits Sangtae Oh, Byong-Gon Park, Jungyeob Ham, Seokjoon Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-Indazol-2-yl-pentanoic acid C12H14N2O2 ÏàËÆ¶È:53.8% Molecules 2006 11 867-889 Synthesis and Structural Characterization of 1- and 2-Substituted Indazoles: Ester and Carboxylic Acid Derivatives F¨¢tima C. Teixeira, H¨¦l¨¨ne Ramos, In¨ºs F. Antunes, M. J. Curto, M. T. Duarte and Isabel Bento Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-(2-hydroxypropyl)-4-(hexa-2E,4E-dien-6-yl)furan-2(5H)-one ÏàËÆ¶È:53.8% Journal of Natural Products 1991 Vol 54 396 New Antibiotics from Strains of Trichoderma harzianum Faramak Almassi, Emilio L. Ghisalberti, Melissa J. Narbey, Krishnapillai Sivasithamparam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-(2-hydroxypropyl)-4-(2-hexadienyl)-2(5H)-furanone C13H18O3 ÏàËÆ¶È:53.8% Phytochemistry 1992 31 485-486 Inhibitory furanone produced by the biocontrol agent Trichoderma harzianum Arie Ordentlich, Zeev Wiesman, Hugo E. Gottlieb, Miriam Cojocaru, Ilan Chet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . harzianolide C13H18O3 ÏàËÆ¶È:53.8% Phytochemistry 1991 30 3802-3803 Harzianolide, a butenolide metabolite from cultures ofTrichoderma harzianum Norman Claydon, James R. Hanson, Almaz Truneh, Anthony G. Avent Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (¡À)-(4R,6R)-6-benzyl-tetrahydro-4-methoxy-2H-pyran-2-carbonitrile (minor diastereomer) C14H17O2N ÏàËÆ¶È:53.8% Heterocycles 2007 74 447-459 Electrophile-Induced Ether Transfer: An Expedient Route to 2-Cyanotetrahydropyrans Rendy Kartika and Richard E. Taylor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 6,10-dimethyl-5,9-undecudien-2,8-dione C13H20O2 ÏàËÆ¶È:53.8% Phytochemistry 1980 19 2759-2760 A geranylacetone derivative from the brown alga Cystoseira crinita Vincenzo Amico, Giovanna Oriente, Mario Piattelli, Giuseppe Ruberto, Corrado Tringali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2b C13H20O2 ÏàËÆ¶È:53.8% Tetrahedron Letters 2001 42 5455-5457 Chemical synthesis of optically active cis-cyclohexa-3,5-diene-1,2-diols and their 5-2H-derivatives Takeshi Hanazawa, Sentaro Okamoto, Fumie Sato Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (3¦Â,4¦Á,5¦Á,6¦ÁH,7E,9S)-3,4-dihydroxy-5,6-dihydro-¦Â-ionol C13H24O3 ÏàËÆ¶È:53.8% Chinese Journal of Medicinal Chemistry 2006 16 240-243 Isolation and identification of the chemical constituents from Cephalomappa sinensis MEI Wen-li, DAI Hao-fu, WU Da-gang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ethyl 4-acetyl-6-chloro-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate C13H14NO4Cl ÏàËÆ¶È:53.8% Heterocycles 2001 55 1873-1888 Regioselective Formylation of Ethyl 3,4-Dihydro-2H-1,4- benzoxazine-2-carboxylate or 2-Acetate Derivatives Stanislas Mayer, G¨¦rald Guillaumet, and Jean-Yves M¨¦rour Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (3S,5S)-6-(4-methoxybenzyl)oxy-3-hydroxy-5-methylhex-1-yne C15H20O3 ÏàËÆ¶È:53.8% Tetrahedron 2013 69 387-394 Stereoselectivity of model C22¨C23 aldol coupling for spirangiens A & B Claire Gregg, Michael V. Perkins Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . N1-(3-bromo-4-methylphenyl)-N2-(2,2,6,6-tetramethylpiperidin-4-yl)oxalamide C18H26BrN3O2 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2013 21 2518-2526 CD4 mimics as HIV entry inhibitors: Lead optimization studies of the aromatic substituents Tetsuo Narumi, Hiroshi Arai, Kazuhisa Yoshimura, Shigeyoshi Harada, Yuki Hirota, Nami Ohashi, Chie Hashimoto, Wataru Nomura, Shuzo Matsushita, Hirokazu Tamamura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 5,9,12,16-tetramethylicosa-5,15-diene-9,12-diol ÏàËÆ¶È:53.8% Journal of Chemical Ecology 2012 38 814-824 The Male-produced Sex Pheromone of the True Bug, Phthia picta, is an Unusual Hydrocarbon Rafael A. Soldi, Mauro A. C. M. Rodrigues, Jeffrey R. Aldrich, Paulo H. G. Zarbin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 5-methoxy-2,7-dimethyl-3,4-dihydro-2H-naphthalen-1-one C13H16O2 ÏàËÆ¶È:53.8% The Journal of Organic Chemistry 2004 69 2773-2784 Synthesis of ((+/-)-Hamigeran B, (-)-Hamigeran B, and ((+/-)-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon-Oxygen Bond from Hydrogenolysis Derrick L. J. Clive and Jian Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (S)-4-(3-methoxy-4-methylphenyl)pentanenitrile ÏàËÆ¶È:53.8% Natural Product Communications 2013 8 863-868 Enantioselective Synthesis of Natural Trinorsesquiterpene Tetralones by Chemoenzymatic Approaches Stefano Serra Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 7c(isomer b) ÏàËÆ¶È:53.8% Chemical Research in Toxicology 2013 26 794-802 Thiolactone Sulfoxides as New Reactive Metabolites Acting as Bis-Electrophiles: Implication in Clopidogrel and Prasugrel Bioactivation Patrick M. Dansette, * Dan Levent, Assia Hessani, Gildas Bertho, and Daniel Mansuy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . (E)-6,10-dimethylundeca-5,9-dien-2-one C13H22O ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1988 41 49-56 Terpenoids From the Brown Alga Cystophora moniliformis IA Vanaltena Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-12-10 14:49:23













»Ø¸´´ËÂ¥