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ÈܼÁ¾ùΪ뮴úÂÈ·Â 1. 23.528,24.363,25.107,25.699,26.807,27.725,34.995,40.163,44.148,45.385,48.602,73.790,81.424,108.327,150.377 2. 10.202,22.147,24.439,27.057,27.255,31.444,34.176,36.930,40.148,47.472,48.913,72.781,79.322,106.855,148.882 3. 13.101,21.039,22.815,25.835,26.427,28.567,39.017,40.550,40.869,45.711,52.989,71.619,79.459,108.357,150.324 |
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²éѯ½á¹û£º¹²²éµ½311¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . cyclonerodiol oxide C15H29O3 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1984 32 4419-4425 Fungal Metabolites. II. Structural Elucidation of Minor Metabolites, Valinotricin, Cyclonerodiol Oxide, and Epicyclonerodiol Oxide, from Trichoderma polysporum TETSURO FUJITA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSUJI FUJIYAMA and TAKAHITO NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Trichoderiol B C15H28O3 ÏàËÆ¶È:66.6% Fitoterapia 2011 82 1035-1038 Sesquiterpenoids from Trichoderma atroviride, an endophytic fungus in Cephalotaxus fortunei Cheng-Jian Zheng, Pei-Xin Sun, Gui-Lin Jin, Lu-Ping Qin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . pestalotheol A C16H24O6 ÏàËÆ¶È:62.5% Journal of Natural Products 2008 71(4) 664-668 Pestalotheols A#D, Bioactive Metabolites from the Plant Endophytic Fungus Pestalotiopsis theae Erwei Li, Renrong Tian, Shuchun Liu, Xulin Chen, Liangdong Guo, and Yongsheng Che Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (7¦Á,9¦Á,10¦Á)-9,10-epoxy-eremophilan-11-ol C15H26O2 ÏàËÆ¶È:60% Helvetica Chimica Acta 2008 Vol. 91 1712 Two New Eremophilane-Type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana (Hemsl.) Greenm Cai-FangWang, Yu Zhao, Yan-Ze Liu, and Zhen-Zhong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 3¦Á-hydroxy-epiilicic acid C15H24O4 ÏàËÆ¶È:60% Journal of Natural Products 1998 61 798-800 New Sesquiterpenoids from the Jordanian Medicinal Plant Inula viscosa Musa H. Abu Zarga, Emad M. Hamed, Salim S. Sabri, Wolfgang Voelter, and Klaus-Peter Zeller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ¦Â-eudesmol C15H26O ÏàËÆ¶È:60% Planta Medica 1987 53 293-294 A Further Contribution to the Sesquiterpenoid Constituents of Cymbopogon proximus M. Hanni Elgamal and Peter Wolff Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . epicyclonerodiol oxide C15H29O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1984 32 4419-4425 Fungal Metabolites. II. Structural Elucidation of Minor Metabolites, Valinotricin, Cyclonerodiol Oxide, and Epicyclonerodiol Oxide, from Trichoderma polysporum TETSURO FUJITA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSUJI FUJIYAMA and TAKAHITO NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Gymnomitr-3(15)-en-5¦Á-ol ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2002 4 281-285 A NEW GYMNOMITRANE-TYPE SESQUITERPENOID FROM THE LIVERWORT CYLINDROCOLEA RECURVIFOLIA CHIA-LI WU and TSUEI-LIEN KAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . chrysanthemol ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2001 3 103-116 Stereoselective Total Synthesis of Chrysanthemol LI-YUAN MOU, LI-YA ZHU, ZI-YUN LIN and XIAO-TIAN LIANG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . amorpha-4,11-diene ÏàËÆ¶È:60% Phytochemistry 1999 52 843-854 Amorpha-4,11-diene synthase catalyses the first probable step inartemisinin biosynthesis Harro J. Bouwmeester, T. Eelco Wallaart, Michiel H.A. Janssen, Bert van Loo, Ben J.M. Jansen, Maarten A. Posthumus, Claus O. Schmidt, Jan-Willem De Kraker, Wilfried A. König, Maurice C.R. Franssen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . chrysanthemol C15H26O2 ÏàËÆ¶È:60% Acta Pharmaceutica Sinica 1987 Vol 22 837-840 STUDIES ON THE CHEMICAL CONSTITUENTS OF CHRYS SANTHEMUM INDICUM L. YU De-Quan and XIE Feng-Zhi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Eudesm-4(14)-ene-3¦Á,11-diol C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1996 41 243-246 Two guaiane and eudesmane-type sesquiterpenoids from Neocallitropsis pancheri Phila Raharivelomanana, Jean-Pierre Bianchini, Robert Faure, Aim¨¦ Cambon, Marcel Azzaro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 11-dihydroxyguaiane C15H26O ÏàËÆ¶È:60% Phytochemistry 1994 36 695-698 Sesquiterpenes and other constituents from chilean mutisieae M. Bittner, M. Silva, Z. Rozas, F. Papastergiou, J. Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . rosacorenone derivative ÏàËÆ¶È:60% Phytochemistry 1991 30 3729-3739 Carotanoids and an acoranoid fromRosa rugosa leaves Yasuyuki Hashidoko, Satoshi Tahara, Junya Mizutani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 5¦Á,7¦ÁH-eudesm-11(13)-en-4¦Á-ol ÏàËÆ¶È:60% Phytochemistry 1991 30 3661-3668 Sesquiterpene lactones fromArtemisia barrelieri J. Alberto Marco, Juan F. Sanz, Alberto Yuste, Miguel Carda, Jasmin Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2,2'-(5',5''-(1,4-diiodobutane-1,4-diyl)bis(2,5'-dimethyl-octahydro-2,2'-bifuran-5',5-diyl))dipropan-2-ol C30H52I2O6 ÏàËÆ¶È:60% Molecules 2011 16 5362-5373 Isolation of a Bis-Iodurated Tetra-THF as a Trace Product from the Oxidation of Squalene with RuO4 and Its Double Ring Expansion to a Novel bis-THF-bis-THP Compound Vincenzo Piccialli, Sabrina Zaccaria, Roberto Centore, Angela Tuzi, Nicola Borbone and Giorgia Oliviero Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . ¦Â-eudesmol ÏàËÆ¶È:60% Phytochemistry 1988 27 2199-2204 Sesquiterpenoid glycosides and an acetogenin glucoside from Lessingia glandulifera Shivanand D. Jolad,Barbara N. Timmermann,Joseph J. Hoffmann,Robert B. Bates,Fernando A. Camou,Teruna J. Siahaan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 11-hydroxyjasionone C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1988 27 3875-3877 11-Hydroxyjasionone,a new sesquiterpene type from Jasonia montana A.A. Ahmed,J. Jakupovic,F. Eid,A.A. Ali Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . ß-eudesmol C15H26O ÏàËÆ¶È:60% Indian Journal of Chemistry Section B 2005 44B 1922-1926 Composition of a new chemotype of Tanacetum nubigenum Chanotiya,C S; Sammal,S S; Mathela,C S Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . selin-11-en-4¦Á-ol C15H26O ÏàËÆ¶È:60% Indian Journal of Chemistry Section B 2005 44B 1922-1926 Composition of a new chemotype of Tanacetum nubigenum Chanotiya,C S; Sammal,S S; Mathela,C S Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Eudesm-5-en-11-ol C15H26O ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2004 42 983-984 Eudesm-5-en-11-ol from Helichrysum italicum essential oil Ange Bianchini, F¨¦lix Tomi, Pascal Richomme, Antoine-François Bernardini and Joseph Casanova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 4(14)-eudesmene-3¦Á,11-diol ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2001 32 778-780 Studies on chemical constituents of Cipadessa baccifera LUO Xiao dong; WU Shao hua; MA Yun bao; WU Da gang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . compound 1 ÏàËÆ¶È:60% Pharmazie 2002 57 59-61 Microbiological conversion of a - and -eudesmol mixture by Rhizopus G.T. Maatooq - J.J. Hoffmann Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-11-14 20:16:07
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²éѯ½á¹û£º¹²²éµ½331¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . ent-4(15)-eudesmen-1¦Á,11-diol C15H26O2 ÏàËÆ¶È:100% Journal of Natural Products 2009 72 1720-1722 ¦Ã-Lactones and ent-Eudesmane Sesquiterpenes from the Endophytic Fungus Eutypella sp. BCC 13199 Masahiko Isaka, Somporn Palasarn, Sanisa Lapanun, Rungtiwa Chanthaket, Nattawut Boonyuen, and Saisamorn Lumyong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 1¦Â-Hydroxy-¦Â-eudesmol C15H26O2 ÏàËÆ¶È:100% Molecules 2003 8 670-677 Sesquiterpenes from Cymbopogon proximus Hesham I. El-Askary, Meselhy R. Meselhy and Ahmed M. Galal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Selin-4(15)-en-1¦Â,11-diol C15H26O2 ÏàËÆ¶È:93.3% Phytochemistry 1982 21 1083-1085 A new sesquiterpene alcohol from Pterocarpus marsupium Dama Adinarayana, Kodakandla Venkata Syamasundar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3-Eudesmene-1¦Â-11-diol C15H26O2 ÏàËÆ¶È:73.3% Phytochemistry 1995 39 603-607 Sesquiterpenes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1¦Â-Acetoxy-4(15)-eudesmen-11-ol C17H28O3 ÏàËÆ¶È:70.5% Phytochemistry 1995 39 603-607 Sesquiterpenes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (+)-Comosol C15H24O2 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2008 56(12) 1710-1716 Structures of New Sesquiterpenes from Curcuma comosa Fengming XU,Seikou NAKAMURA,Yang QU,Hisashi MATSUDA,Yutana PONGPIRIYADACHA,Lijun WU,and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (-)-Comosol C15H24O2 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2008 56(12) 1710-1716 Structures of New Sesquiterpenes from Curcuma comosa Fengming XU,Seikou NAKAMURA,Yang QU,Hisashi MATSUDA,Yutana PONGPIRIYADACHA,Lijun WU,and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ¦Â-dictyopterol ÏàËÆ¶È:66.6% Phytochemistry 1997 44 1287-1290 Sesquiterpenoid alcohols from Chrysanthemum morifolium Lihong Hu, Zhongliang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 4(15)-Eudesmene-1¦Â,11-diol C15H26O2 ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung B 2007 62b 267-271 Sesquiterpenes and Phenolic Compounds from Achillea clypeolata Ingrid Werner, Pavel Mucaji, Armin Presser, and Sabine Glasl Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . microbiotol C14H23O ÏàËÆ¶È:66.6% Indian Journal of Chemistry Section B 2007 46B 805-817 Total synthesis of (¡À)-¦Â-microbiotene,(¡À)-microbiotol,(¡À)-cyclocuparanol and (¡À)-¦Â-cuparenones Srikrishna,A; Ramachary,D B Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . ¦Â-Dictyopterol C15H24O ÏàËÆ¶È:66.6% Pharmazie 2005 60 155-159 Three new polymeric isopropenyl benzofurans from Ligularia stenocephala Fu-Lin Yan, Ai-Xia Wang, and Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . ¦Â-Dictyopterol ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2004 27 164-168 Pytochemical constituents of the aerial parts from solidago virga-aurea var. gigantea Sang Zin Choi, Sang Un Choi and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 4(15),11-Eudesmadiene-1¦Â-ol C15H24O ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2010 46 661-663 Sesquiterpenes and triterpenes from Aeschynanthus mengxinggensis Wen-Yi Kang, Lin Chen and Xin-Yan Zang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . ¦Á-Eudesmol ÏàËÆ¶È:66.6% Flavour and Fragrance Journal 2000 15 421-431 Hydrolysis of hedycaryol: the origin of the eudesmols in the Myrtaceae Charles P Cornwell, Narsimha Reddy, David N Leach and S Grant Wyllie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . ent-4(15)-eudesmen-11-ol-1-one C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2009 72 1720-1722 ¦Ã-Lactones and ent-Eudesmane Sesquiterpenes from the Endophytic Fungus Eutypella sp. BCC 13199 Masahiko Isaka, Somporn Palasarn, Sanisa Lapanun, Rungtiwa Chanthaket, Nattawut Boonyuen, and Saisamorn Lumyong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (4R)-3¦Á-hydroxycadin-10(15)-ene C15H26O ÏàËÆ¶È:60% Phytochemistry 2000 54 39-45 Biotransformation of cadinane sesquiterpenes by Beauveria bassiana ATCC 7159 Greg O. Buchanan, Lawrence A.D. Williams, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 7¦Á-hydroxyguaioxide C15H26O2 ÏàËÆ¶È:60% Phytochemistry 1999 51 757-760 The hydroxylation of the sesquiterpenoid guaioxide by Mucor plumbeus Simone Fontes Arantes, James R. Hanson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 11-dihydroxyguaiane C15H26O ÏàËÆ¶È:60% Phytochemistry 1994 36 695-698 Sesquiterpenes and other constituents from chilean mutisieae M. Bittner, M. Silva, Z. Rozas, F. Papastergiou, J. Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . homalomenol B C15H26O2 ÏàËÆ¶È:60% Phytochemistry 1992 31 3515-3520 Sesquiterpenoids from the roots of Homalomena aromatica T.V. Sung, B. Steffan, W. Steglich, G. Klebe, G. Adam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 2,2'-(5',5''-(1,4-diiodobutane-1,4-diyl)bis(2,5'-dimethyl-octahydro-2,2'-bifuran-5',5-diyl))dipropan-2-ol C30H52I2O6 ÏàËÆ¶È:60% Molecules 2011 16 5362-5373 Isolation of a Bis-Iodurated Tetra-THF as a Trace Product from the Oxidation of Squalene with RuO4 and Its Double Ring Expansion to a Novel bis-THF-bis-THP Compound Vincenzo Piccialli, Sabrina Zaccaria, Roberto Centore, Angela Tuzi, Nicola Borbone and Giorgia Oliviero Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-11-14 20:17:12
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²éѯ½á¹û£º¹²²éµ½372¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . cyperusol C C15H26O2 ÏàËÆ¶È:100% Journal of Natural Products 2004 67 569-576 Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Cyperusol C C19H28O2 ÏàËÆ¶È:100% The Journal of Antibiotics 2010 63 245-250 Terpenoids produced by actinomycetes: isolation, structural elucidation and biosynthesis of new diterpenes, gifhornenolones A and B from Verrucosispora gifhornensis YM28-088 Masato Shirai, Masaaki Okuda, Keiichiro Motohashi, Masaya Imoto, Kazuo Furihata, Yoshihide Matsuo, Atsuko Katsuta, Yoshikazu Shizuri and Haruo Seto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 4 ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2012 10 358-362 A new 1, 10-secoguaianolide from the aerial parts of Artemisia anomala Ke ZAN, Xiao-Qing CHEN, Peng-Fei TU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 11-Eudesmene-1¦Â,4¦Á-diol C15H26O2 ÏàËÆ¶È:93.3% Chemistry of Natural Compounds 2010 46 661-663 Sesquiterpenes and triterpenes from Aeschynanthus mengxinggensis Wen-Yi Kang, Lin Chen and Xin-Yan Zang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (1¦Â,4¦Á,6¦Â)-Gorgonane-1¦Â,4¦Á,11-triol C15H28O3 ÏàËÆ¶È:80% Helvetica Chimica Acta 2013 96 445-451 Six Novel Eudesmane-Like Sesquiterpenes from Illicium spathulatum Xu-Jun Dong and Shi-De Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol C15H26O3 ÏàËÆ¶È:73.3% Natural Medicines 2001 55 87-89 A New Eudesmane Sesquiterpene from the Fruit Body oiLactarius laeticolorus Yoshikawa Kazuko,Tori Kanako,Arihara Shigenobu,Sasaki Takuma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (1S,3¦ÁR,4- S,8¦ÁS,9S)-Decahydro-4,8,8-trimethyl-1,4-methanoazulene-9-carboxylic Acid ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2003 Vol. 86 106 The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 1¦Â,4¦Â-dihydroxyeudesman-11-ene C15H26O2 ÏàËÆ¶È:66.6% Planta Medica 2005 71 268-272 New Sesquiterpenes from Erigeron annus Li, Xin; Yang, Min; Han, Yi-Feng; Gao, Kun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . hedytriol C15H28O3 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . capitulatin B C15H26O2 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2005 7 279-282 Capitulatin B, A new eudesmane derivative from Curculigo capitulata, and revised assignment of 13C NMR data of 6a,15a-epoxy-1b,4b-dihydroxyeudesmane NING LI, JI-JUN CHEN and JUN ZHOU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . acrostalic acid ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2009 92 1118-1125 Labdane and Tetranorlabdane Diterpenoids from Botryosphaeria sp. MHF, an Endophytic fungus of Maytenus hookeri Lin Yuan, Pei-Ji Zhao, Juan Ma, Chun-Hua Lu, Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . ¦Â-Helmiscapene ÏàËÆ¶È:60% Phytochemistry 2005 66 941-949 Composition of the essential oil of the liverwort Radula perrottetii of Japanese origin Hailemichael Tesso, Wilfried A. König, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . li-selinen-4-ol ÏàËÆ¶È:60% Planta Medica 1995 61 196-197 Isolation and Identification of 11- Selinen-4¦Á,7¦Â-ol and 10-Aromadendranolin the Essential Oil of Murraya koenigii I. Wa¦Âmuth- Wagner, H.-O. Kalinowski. andH. fork Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Unlabelled gymnomitr-3(15)-en-4¦Á-ol ÏàËÆ¶È:60% Phytochemistry 2000 53 645-650 Biosynthesis of the gymnomitrane-type sesquiterpenes in liverworts Ute Warmers, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 2a ÏàËÆ¶È:60% Phytochemistry 2000 53 645-650 Biosynthesis of the gymnomitrane-type sesquiterpenes in liverworts Ute Warmers, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 2b ÏàËÆ¶È:60% Phytochemistry 2000 53 645-650 Biosynthesis of the gymnomitrane-type sesquiterpenes in liverworts Ute Warmers, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 29 ÏàËÆ¶È:60% Journal of Natural Products 1992 Vol 55 577 Molecular Rearrangements in the Longipinene Series Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas, Rosa Mar¨ªa Dom¨ªnguez-L¨®pez, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (lR,5R,6R,8S)-dec[4.4.0]ane-1,5-dimethyl-8-( l'-methylethenyl)-5-isothiocyanate C16H25SN ÏàËÆ¶È:60% Journal of Natural Products 1992 Vol 55 633 Two New Sesquiterpene Isothiocyanates from the Marine Sponge Acanthella klethra Gabriele M. König, Anthony D. Wright, Otto Sticher, Frank R. Fronczek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . aldebyde ÏàËÆ¶È:60% Journal of Natural Products 1993 Vol 56 1723 A Short Synthesis of (+)-Colartin and (+)-Arbusculin A from (-)-Santonin Gonzalo Blay, Luz Cardona, Begoña Garcia, Jose R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 3 C15H28O3 ÏàËÆ¶È:60% Phytochemistry 1995 40 853-855 Boarioside, a eudesmane glucoside from Maytenus boaria O. Muñoz, C. Galeffi, E. Federici, J. A. Garbarino, M. Piovano, M. Nicoletti Structure 13C NMR ̼Æ×Ä£Äâͼ |
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