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²éѯ½á¹û£º¹²²éµ½33¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 3 ÏàËÆ¶È:60% Chemical Communications 1977 27-28 Vetispirane sesquiterpene glucosides from flue-cured virginia tobacco: structure, absolute stereochemistry, and synthesis. X-Ray structure of the p-bromobenzenesulphonate of one of the derived aglycones Robert C. Anderson, Donald M. Gunn, Judith Murray-Rust, Peter Murray-Rust and James S. Roberts Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 13-hydroxy-3,11-(7¦ÁH,10¦ÂH)-acordien-3-one C15H22O2 ÏàËÆ¶È:60% Journal of Chemical Research 2007 31 38-39 A new sesquiterpene from the seeds of Physalis alkekengi L. var. franchi Zhan, Zha-Jun; Li, Cheng-Ping; Shan, Wei-Guang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . dihydroestafiatone C15H20O3 ÏàËÆ¶È:53.3% Phytochemistry 2003 1101-1104 Microbial transformation of zaluzanin-D G.N. Krishna Kumari, S. Masilamani, M.R. Ganesh, S. Aravind Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . luzonenone C15H22Br2O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2005 68 1314-1317 Terpenoids from Laurencia luzonensis Masayuki Kuniyoshi, Paul G. Wahome, Takayuki Miono, Takeshi Hashimoto, Muneaki Yokoyama, Keshab L. Shrestha, and Tatsuo Higa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . canusesnol J C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 1893-1896 New Sesquiterpenes from Capsicum annuum Yousuke Kawaguchi, Toshimasa Ochi, Yoshihisa Takaishi, Kazuyoshi Kawazoe, and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2¦Â,12-dihydroxy-13,14,15,16,17-pentanor-ent-labdane-8-one ÏàËÆ¶È:53.3% Molecules 2007 12 2605-2620 Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II Luis E. Catal¨¢n, Karen C. Mar¨ªn, H¨¦ctor C. Altamirano, Mauricio C. Fritis and Mar¨ªa C. Chamy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . pedunculoside ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 1993 18 226-228 Studies on Constituents of Ilex chinensis Sims Zhao Haoru, Wang Mingshi and Zhou Guoping Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 4 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 977-979 Oplopanes from the leaves of Senecio mexicanus Pedro Joseph-Nathan,J.Roberto Villag¨®mez,Luisa U. Rom¨¢n,Juan D. Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (¡À)-1,1,4a¦Á,7¦Á-tetramethyl-2,3,4,4a,5,6,7,8-octahydro-1H-benzocycloheptene-5,7-diol C15H26O2 ÏàËÆ¶È:53.3% 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 -------------------------------------------------------------------------------- 10 . 1,2,3,5,6,7,8,8a-octahydro-3-[(2S)-1-hydroxypropan-2-yl]-5,8a-dimethylnaphthalen-2-ol C15H26O2 ÏàËÆ¶È:53.3% Chemistry & Biodiversity 2010 7 1681-1697 Structure¨CActivity Relationship Studies on Derivatives of Eudesmanolides from Inula helenium as Toxicants against Aedes aegypti Larvae and Adults Charles L. Cantrell, Julia W. Pridgeon, Frank R. Fronczek and James J. Becnel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . trichothecolone ÏàËÆ¶È:53.3% Phytochemistry 1978 17 427-430 The biosynthesis of trichothecin from acetate- [1,2- 13C2] Brian Dockerill, James R. Hanson, Michael Siverns Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Trichothecolone ÏàËÆ¶È:53.3% Archives of Pharmacal Research 2008 31 611-616 Cytotoxic activities of trichothecenes isolated from an endophytic fungus belonging to order hypocreales Maneekarn Chinworrungsee, Suthep Wiyakrutta, Nongluksna Sriubolmas, Phitaya Chuailua and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 6-oxodrimanol ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 1980 221-226 Fungal metabolites. Part 5. Uvidins, new drimane sesquiterpenes from Lactarius uvidus Fries Maria De Bernardi, Giorgio Mellerio, Giovanni Vidari, Paola Vita-Finzi and Giovanni Fronza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (5R,6S,7R)-6,7,11,11-tetramethyldispiro[3.0.4.2]undecan-6-ol C15H26O ÏàËÆ¶È:53.3% Tetrahedron 1995 51 8835-8852 Synthesis of tricyclopentanoid sesquiterpenes via rearrangement routes: (¡À)-modhephene, (¡À)-epimodhephene and (¡À)-isocomene Lutz Fitjer, Marita Majewski, Honorato Monz¨®-Oltra Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . tsangane J C15H26O3 ÏàËÆ¶È:53.3% Tetrahedron 1999 55 759-770 Allohimachalane, seco-allohimachalane and himachalane sesquiterpenes from Illicium tsangii Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 9-[(1R*,2S*,6R*,7R*,8S*)-4-thiatricyclo[5.2.1.0(2,6)]dec-8-yl]-9H-purin-6-amine C14H17N5S ÏàËÆ¶È:53.3% Tetrahedron 2012 68 3195-3204 Synthesis of novel thienonorbornylpurine derivatives Hubert Hřebabecký, Milan Dejmek, Michal Ѝ¢la, Helena Mertl¨ªkov¨¢-Kaiserov¨¢, Martin Drač¨ªnský, Pieter Leyssen, Johan Neyts, Radim Nencka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 1 C15H25BrO ÏàËÆ¶È:53.3% Journal of Chemical Ecology 1993 19 1847-1860 Isolation of new brominated sesquiterpene feeding deterrents from tropical green algaNeomeris annulata (Dasycladaceae: Chlorophyta) Valerie J. Paul, John M. Cronan and John H. Cardellina Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (1S,7R)-4-oxa-7,11,11-trimethylbicyclo[5.4.0]undecan-3-one C13H22O2 ÏàËÆ¶È:53.3% Journal of Agricultural and Food Chemistry 1993 41 2097-2103 New lactones from tobacco Tore. Pettersson, Ann Marie. Eklund, Inger. Wahlberg Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (3aR,5S,8aR,9aR)-3-[(diethylamino)methyl]-3a,5,6,7,8,8a,9,9a-octahydro-5,8a-dimethyl-naphtho[2,3-b]furan-2(3H)-one C19H31NO2 ÏàËÆ¶È:52.9% Chemistry & Biodiversity 2010 7 1681-1697 Structure¨CActivity Relationship Studies on Derivatives of Eudesmanolides from Inula helenium as Toxicants against Aedes aegypti Larvae and Adults Charles L. Cantrell, Julia W. Pridgeon, Frank R. Fronczek and James J. Becnel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 2¦Á-hydroxystemod-12-ene ÏàËÆ¶È:50% Phytochemistry 2004 65 701-710 Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145 Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . ent-1¦Á-hydroxyrhizop-15-en-18-oic acid C20H28O3 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 1121-1125 Rearranged Diterpenoids from the Biotransformation of ent-Trachyloban-18-oic Acid by Rhizopus arrhizus Aur¨¦lie Leverrier, Marie-Th¨¦r¨¨se Martin, Claudine Servy, Jamal Ouazzani, Pascal Retailleau, Khalijah Awang, Mat Ropi Mukhtar, Françoise Gu¨¦ritte and Marc Litaudon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . compound 2c ÏàËÆ¶È:50% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 14¦Á,16-oxido-ent-isopimar-7-ene-6,15-dione ÏàËÆ¶È:50% Journal of Natural Products 1992 Vol 55 1477 Diterpenes of Calibrachoa parviflora Carl A. Elliger, Rosalind Y. Wong, Mabry Benson, William Gaffield, Anthony C. Waiss Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 14 ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 10353-10356 A stereocontrolled total synthesis of (¡À)-norzizanone Lokesh Chandra Pati, Arnab Roy, Debabrata Mukherjee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 7¦Á-hydroxy-14,15-dinor-13-oxo-8(17)-labdene ÏàËÆ¶È:50% Phytochemistry 1990 29 321-323 Diterpenes and other constituents of Eupatorium salvia Antonio G. Gonz¨¢lez,Jaime Bermejo Barrera,Jes¨²s G. D¨ªaz,Elsa Ma Rodriguez P¨¦rez,Angel C. Yanes,Pilar Rauter,Jaime Pozo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . compound 11 ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1976 114-117 The 13C nuclear magnetic resonance spectra of kauranoid diterpenes James R. Hanson, Michael Siverns, Franco Piozzi and Giuseppe Savona Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . compound 12 ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1976 114-117 The 13C nuclear magnetic resonance spectra of kauranoid diterpenes James R. Hanson, Michael Siverns, Franco Piozzi and Giuseppe Savona Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . compound 68 ÏàËÆ¶È:50% Heterocycles 2001 54 529-559 Biotransformation of Terpenoids from the Crude Drugs and Animal Origin by Microorganisms Toshihiro Hashimoto, Yoshiaki Noma, and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . (+)-(3aS,5S,5aS,9aS,9bR)-3a-(hydroxymethyl)-6,6,9a-trimethyldodecahydronaphtho[2,1-b]furan-5-ol C16H28O3 ÏàËÆ¶È:50% Tetrahedron 2001 57 5663-5679 The synthesis of Ambrox®-like compounds starting from (+)-larixol Marjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . (-)-(3aR,9aR,9bR)-3a,6,6,9a-tetramethyl-1,2,3a,4,6,7,8,9,9a,9b-decahydronaphtho[2,1-b]furan C16H26O ÏàËÆ¶È:50% Tetrahedron 2001 57 5663-5679 The synthesis of Ambrox®-like compounds starting from (+)-larixol Marjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . compound 13 ÏàËÆ¶È:50% Organic Magnetic Resonance 1982 18 138-142 13C NMR spectra of wedeloside and related kaurenoid derivatives I. A. S. Lewis and J. K. MacLeod Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . compound 139 ÏàËÆ¶È:50% Natural Product Communications 2008 3 399-412 Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 15-Didehydroatractyligenin Methyl Ester ÏàËÆ¶È:50% Journal of Natural Products 2012 75 1070-1075 Structural Characterization and Antimicrobial Evaluation of Atractyloside, Atractyligenin, and 15-Didehydroatractyligenin Methyl Ester Federico Brucoli, Maria T. Borrello, Paul Stapleton, Gary N. Parkinson, and Simon Gibbons Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

3Â¥2012-09-02 07:57:51













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