| ²é¿´: 798 | »Ø¸´: 3 | |||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | |||
Ñî´óËÉÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
|
||
|
̼Æ×Êý¾ÝÈçÏ£º 17.6,18.4,22.3,22.9,25.6,33.9,38.0,38.4,39.1,72.4,73.3,122.9,123.3 ÐÁ¿à¸÷λÁË£¬Ð»Ð» |
» ²ÂÄãϲ»¶
±¾ÈË¿¼085602 »¯Ñ§¹¤³Ì ר˶
ÒѾÓÐ15È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
274Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
302Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
11408 Ò»Ö¾Ô¸Î÷µç£¬277·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
»¯Ñ§¹¤³Ì321·ÖÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
341Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏÓ뻯¹¤304ÇóBÇøµ÷¼Á
ÒѾÓÐ7È˻ظ´
0703»¯Ñ§336·ÖÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
[¸´ÊÔµ÷¼Á]Î÷ÄϿƼ¼´óѧ¹ú·À/²ÄÁϵ¼Ê¦ÍƼö
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖúÈýÝÆ»¯ºÏÎï½âÎö£¡²»Éõ¸Ð¼¤
ÒѾÓÐ38È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÔÚexcelÀï´¦ÀíÒ»ÏÂÊý¾ÝÇó΢·Ö£¬Çë¸ßÊÖÖ¸½ÌÒ»ÏÂ~ллÀ²~
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿Î¢·´-É«Æ× ÔõôʹÓ𡣿
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿¶à´ÎÖÊÆ×½á¹û±»ËÜÁÏÎÛȾ
ÒѾÓÐ3È˻ظ´

»ð¼ý´©Æ¨Æ¨
ľ³æ (ÕýʽдÊÖ)
µØÇòÇò³¤
- Ó¦Öú: 197 (¸ßÖÐÉú)
- ½ð±Ò: 3684.8
- ºì»¨: 8
- Ìû×Ó: 529
- ÔÚÏß: 194.4Сʱ
- ³æºÅ: 407719
- ×¢²á: 2007-06-20
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶¹¸ç: ½ð±Ò+4, лл²ÎÓë 2012-08-29 09:40:39
Ñî´óËÉ: ½ð±Ò+14, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-08-29 14:07:05
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶¹¸ç: ½ð±Ò+4, лл²ÎÓë 2012-08-29 09:40:39
Ñî´óËÉ: ½ð±Ò+14, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-08-29 14:07:05
|
²éѯ½á¹û£º¹²²éµ½103¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 13 ÏàËÆ¶È:64.2% Journal of Natural Products 2011 74 1414-1420 Absolute Configuration of 7-epi-Sesquithujene Ashot Khrimian, Allard A. Coss¨¦, and Damon J. Crook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . cis-(4R,5R)-5-(4'-Methyl-pent-3'-enyl)-4-hydroxy-5-methyl-dihydrofuran-2-one ÏàËÆ¶È:61.5% Natural Product Communications 2011 6 367-370 Synthesis of a Natural ¦Ã-Butyrolactone from Nerylacetone by Acremonium roseum and Fusarium oxysporum Cultures Anna Gliszczy¨½ska, Marta Świtalska, Joanna Wietrzyk and Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Racemosin A C12H20O2 ÏàËÆ¶È:61.5% Planta Medica 2012 78 166-171 Sesquiterpenoids from Inula racemosa Hook. f. Inhibit Nitric Oxide Production Zhang, Shou-De; Qin, Jiang-Jiang; Jin, Hui-Zi; Yin, Yin-Hua; Li, Hong-Lin; Yang, Xian-Wen; Li, Xia; Shan, Lei; Zhang, Wei-Dong: Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (-)-Perfora-1,7-diene C15H24 ÏàËÆ¶È:60% Phytochemistry 2004 65 199-206 Sesquiterpenes of the liverwort Scapania undulata Adewale Martins Adio, Claudia Paul, Petra Kloth, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5¦Â-hydroxycostic acid ÏàËÆ¶È:60% Phytochemistry 2003 63 835-839 Eudesmane and megastigmane glucosides from Laggera alata Qunxiong Zheng, Zhaojun Xu, Xianfeng Sun, Wei Yao, Handong Sun,Christopher H. K. Cheng, Yu Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . incisumdiol B C15H26O2 ÏàËÆ¶È:60% Planta Medica 2008 74 1812-1817 New Guaiane Sesquiterpenes and Furanocoumarins from Notopterygium incisum Shi-BiaoWu, Yun Zhao, Hui Fan, Ying-He Hu, Mark T. Hamann, Jiang-Nan Peng, Courtney M. Starks,Mark O'Neil-Johnson, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (Z)-2-Methylbut-2-enoic acid (1S,2R,4aR,7R,8aR)-1-hydroxy-7-isopropyl-1,4a-dimethyl-6-oxodecahydronaphthalen-2-yl ester C15H26O3 ÏàËÆ¶È:60% Journal of the Chemical Society, Perkin Transactions 1 2000 731-735 Asymmetric synthesis of 3¦Â-angeloyloxy-4¦Â-hydroxyeudesman-8-one, purported sesquiterpene from Pluchea quitoc Estela Muri, Alice Kanazawa, Eliezer Barreiro and Andrew E. Greene Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . teleocidin B-3 C28H41N3O2 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1984 32 4233-4236 ISOLATION AND STRUCTURE ELUCIDATION OF TELEOCIDIN B-1, B-2, B-3, AND B-4 Yukio Hitotsuyanagi,Hirota Fujiki,Masami Suganuma,Norio Aimi,Shinichiro Sakai,Yasuyuki Endo,Koichi Shudo and Takashi Sugimura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (1R,2S,4aS,8aS)-Decahydro-2,5,5,8a-tetramethylnaphthalene-1,2-diol C14H26O2 ÏàËÆ¶È:57.1% Chemistry & Biodiversity 2010 7 421-439 Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry Andres Parra, Pilar E. Lopez and Andres Garcia-Granados Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 11-nor-8,9R-drimanediol C14H26O2 ÏàËÆ¶È:57.1% Acta Chemica Scandinavica 1981 35 307-310 Tobacco Chemistry. 55. Three New Cembranoids from Greek Tobacco. The Stereochemistry of (1S,2E,4S,6R,7E,11E)-2,7,11-Cembratriene-4,6-diol. Wahlberg, Inger; Wallin, Ingrid; Narbonne, Claudine; Nishida, Toshiaki; Enzell, Curt R.; Berg, Jan-Eric Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 12 ÏàËÆ¶È:57.1% Journal of Natural Products 2011 74 1414-1420 Absolute Configuration of 7-epi-Sesquithujene Ashot Khrimian, Allard A. Coss¨¦, and Damon J. Crook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 7'-Multijuguinol C18H31NO2 ÏàËÆ¶È:55.5% Journal of Natural Products 2012 75 408−413 Pyridine Alkaloids from Senna multijuga As Acetylcholinesterase Inhibitors Welington Francisco, Marcos Pivatto, Amanda Danuello, Luis O. Regasini, Luciene R. Baccini,Maria C. M. Young, Norberto P. Lopes, João L. C. Lopes, and Vanderlan S. Bolzani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2-dehydrococcinelline C13H21NO ÏàËÆ¶È:53.8% Journal of Natural Products 1997 60 1148-1149 2-Dehydrococcinelline, a New Defensive Alkaloid from the Ladybird Beetle Anatis ocellata (Coccinellidae) B. Lebrun, J. C. Braekman, D. Daloze, and J. M. Pasteels Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 2,2,6a,7a-Tetramethyl-10-oxatricyclo[5.2.1.0 1 6]decan C13H22O ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1980 63 154-190 Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3-bromo-methyl-3-chloro-7-methyl-1,6-octadiene ÏàËÆ¶È:53.8% Phytochemistry 1976 15 1069-1070 (− -3-Bromomethyl-3-chloro-7-methyl-1, 6-octadiene from Sri Lankan Chondrococcus hornemanniFrank X. Woolard, Richard E. Moore, M. Mahendran, A. Sivapalan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 11,12,13-trinoreudesm-5-en-7¦Â,8¦Á-diol C12H20O2 ÏàËÆ¶È:53.8% Journal of Asian Natural Products Research 2011 Vol.13,No.6 570-574 Sesquiterpenoids from Inula racemosa Li-Wei Xua and Yan-Ping Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Trinoralantolactone C12H20O2 ÏàËÆ¶È:53.8% Tetrahedron 2011 67 9193-9198 Sesquiterpenoids, alantolactone analogues, and seco-guaiene from the roots of Inula helenium Hai-Long Jiang, Jia Chen, Xiao-Jie Jin, Jun-Li Yang, Ya Li, Xiao-Jun Yao , Quan-Xiang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 2,2-bis(isomenthopyrazol-2,2'-yl)propane C25H40N4 ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2003 40 681-688 Asymmetric diels alder reaction using pyrazole derivatives as a chiral catalyst Choji Kashima,Yohei Miwa,Saori Shibata and Hiroyuki Nakazono Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . ethyl (¡À)-(2E)-3-{(1R,2R)-2-[(methanesulfonyloxy)-methyl]cyclohexane}-2-propenoate ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2002 39 1049-1054 Fused-ring nitrogen and sulfur heterocycles by a tandem SN2-michael addition reaction Richard A. Bunce, Sharadsrikar V. Kotturi, Christopher J. Peeples and Elizabeth M. Holt Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 1-Methyl-2,2-ethylenedithiobicyclo[2.2.2]octan-6 endo-ol ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 2007 45 420-423 Spectroscopic characterization of 6-hydroxy and 1-methyl-6-hydroxybicyclo[2.2.2]octan-2-one ethylene acetals and ethylene dithioacetals (pages 420¨C423) Francesca Leonelli, Barbara Garofalo, Angela La Bella, Ermanno Lasta, Francesca Ceccacci, Luisa M. Migneco and Rinaldo Marini Bettolo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Geranyl isopropanol ÏàËÆ¶È:53.8% Magnetic Resonance in Chmesitry 2005 43 176-179 Enantiomeric differentiation of acyclic terpenes by 13C NMR spectroscopy using a chiral lanthanide shift reagent Marie-C¨¦cile Blanc, Pascale Bradesi and Joseph Casanova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . Nonacosane-4,10-diol C29H60O2 ÏàËÆ¶È:53.8% Phytochemistry 1981 20 2711-2716 Epicuticular wax of Juniperus scopulorum Alexander P. Tulloch, Lothar Bergter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . compound 2e ÏàËÆ¶È:53.8% Tetrahedron Letters 2001 42 2481-2484 Preparation of oxetanes by silicon-directed 4-exo trig electrophilic cyclisations of homoallylic alcohols Mazin Rofoo, Marie-Claude Roux, G¨¦rard Rousseau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . (E)-5,9-Dimethyl-4,8-decadienoic acid ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2000 8 2729-2737 2-(Acyloxy)ethylphosphonate analogues of prenyl pyrophosphates: synthesis and biological characterization Diana M. Cermak, David F. Wiemer, Kriste Lewis, Raymond J. Hohl Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 1-(3-methoxy-1-cyclohexen-2-yl)cyclohexanol C13H22O2 ÏàËÆ¶È:53.8% Tetrahedron 2002 58 5163-5172 Six- and five-membered 3-alkoxy-2-lithiocycloalkenes: new stable non-anionic ¦Â-functionalised organolithium compounds Miguel Yus, Diego J Ram¨®n, Inmaculada G¨®mez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . (1S,7R,8R)-8-cyano-1,4-dimethylbicyclo[5.3.0]dec-3-ene C13H19N ÏàËÆ¶È:53.8% The Journal of Organic Chemistry 2002 67 6034-6040 Total Synthesis and Absolute Configuration of Liverwort Diterpenes, (− -13(15)E,16E-3¦Â,4¦Â-Epoxy-18-hydroxysphenoloba-13(15),16-diene and (− -13(15)Z,16E-3¦Â,4¦Â-Epoxy-18-hydroxysphenoloba-13(15),16-diene, by Use of the Ring Closing Metathesis Reaction AppliKatsuyuki Nakashima, Kosuke Inoue, Masakazu Sono, and Motoo Tori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . compound VII ÏàËÆ¶È:53.8% Russian Journal of Organic Chemistry 2003 39 985-991 Acid-Catalyzed Reactions of 2,3-Epoxy Derivatives of Citral with Alcohols O. I. Yarovaya, D. V. Korchagina, O. V. Salomatina, M. P. Polovinka and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . compound VIII ÏàËÆ¶È:53.8% Russian Journal of Organic Chemistry 2003 39 985-991 Acid-Catalyzed Reactions of 2,3-Epoxy Derivatives of Citral with Alcohols O. I. Yarovaya, D. V. Korchagina, O. V. Salomatina, M. P. Polovinka and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 4,10-dihydroxy-10-methyldodecanoic acid C13H26O4 ÏàËÆ¶È:53.8% The Journal of Antibiotics 2008 61 736-746 Electrospray Ionization Mass Spectra of Piperazimycins A and B and -Butyrolactones from a Marine-derived Streptomyces sp.† Khaled A Shaaban, Mohamed Shaaban, Petrea Facey, Serge Fotso, Holm Frauendorf, Elisabeth Helmke, Armin Maier, Heinz H Fiebig and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . eudesm-4(15),7-diene-9¦Á,11-diol C15H24O2 ÏàËÆ¶È:53.3% Phytochemistry 2008 69 2088-2094 Three types of sesquiterpenes from rhizomes of Atractylodes lancea He-Xiang Wang, Chun-Mei Liu, Quan Liu, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . (1R,2R,5S,6S,7S,10S)*-5-epi-eudesm-4(15)-ene-1R,2¦Â,6R-triol C15H26O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2006 69 1618-1621 Cytotoxic cis-Fused Bicyclic Sesquiterpenoids from Jatropha neopauciflora Abraham Garca, and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . (S)-(+)-12-hydroxy-10,11-dihydrocurcuphenol C15H24O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1547-1553 Microbial and Chemical Transformation Studies of the Bioactive Marine Sesquiterpenes (S)-(+)-Curcuphenol and -Curcudiol Isolated from a Deep Reef Collection of the Jamaican Sponge Didiscus oxeata Khalid A. El Sayed,Muhammad Yousaf, Mark T. Hamann, Mitchell A. Avery, Michelle Kelly, and Peter Wipf Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 4,5-seco-11(13)-eudesmen-12,8-olid-4-one C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 466-471 Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 7¦ÂH-eudesm-11-en-3¦Á-ol C15H26O ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 22-28 Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . 7¦ÂH-eudesm-11-en-3¦Â-ol C15H26O ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 22-28 Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . carabrone ÏàËÆ¶È:53.3% Journal of Natural Products 1997 60 550-555 Sesquiterpene Lactones and Thymol Esters from Vicoa pentanema Jaber S. Mossa, Farouk S. El-Feraly, Ilias Muhammad, Kyaw Zaw, Zakaria H. Mbwambo, John M. Pezzuto, and Harry H. S. Fong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . zingiberene-3,6-¦Â-endoperoxide C15H24O2 ÏàËÆ¶È:53.3% Planta Medica 1996 62 565-566 Sesquiterpene Peroxides from Senecio selloi and Eupatorium rufescens G. R¨¹cker, E. P. Scherikel, D. Manns, R. Mayer,K. Heiden, and B. M. Heinzmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . compound 7 ÏàËÆ¶È:53.3% Planta Medica 1999 65 153-156 Sesquiterpene Lactone Glycosides from Arnica longifolia Claus M.Passreiter,Massimo De Carlo,and A.Steigel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . dihydroagarofuran ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1985 33 1148-1153 Agarofuran-, Eudesmane-and Eremophilane-Type Sesquiterpenoids from Alpinia japonica (THUNB.) MIQ. HIDEJI ITOKAWA,HIROSHI MORITA,KINZO WATANABE,SUSUMU MIHASHI and YOICHI IITAKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . granilin ÏàËÆ¶È:53.3% Phytochemistry 1976 15 1531-1532 Granilin and ivasperin from Ambrosia polystachya. 13C-NMR spectra of hydroxylated isoalantones Walter Vichnewski, Ilda Kazumi Shuhama, Richard C. Rasanske, Werner Herz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . carabrone ÏàËÆ¶È:53.3% Natural Product Research 2007 21 824-827 Sesquiterpene compounds from Inula viscosa Gianfranco Fontana; Salvatore La Rocca; Salvatore Passannanti; Maria Pia Paternostro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . 6¦Á,7¦Á,10¦Á-trihydroxyisoducane C15H28O3 ÏàËÆ¶È:53.3% Natural Product Research 2009 23 1279-1283 A new sesquiterpenoid from rhizomes of Homalomena occulta Y. M. Hu; Z. L. Yang; H. Wang; W. C. Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . eudesm-3¦Â,4¦Â,11-triol ÏàËÆ¶È:53.3% Phytochemistry 1999 52 689-694 A revision of the positive sign of the optical rotation and its maximum value of ¦Á-eudesmol Masao Toyota, Yumiko Yonehara, Isao Horibe, Kazuyuki Minagawa, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . N-methyl-2-(2-hydroxybutyl)-6-(2-hydroxypentyl)-piperidine C15H31NO2 ÏàËÆ¶È:53.3% Phytochemistry 1998 48 911-913 Piperidine alkaloids and other constituents of Dialypetalum floribundum Hans C. Krebs, Harisolo Ramiarantsoa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . trans-dihydroagarofuran ÏàËÆ¶È:53.3% Phytochemistry 1997 45 307-311 Variability of essential oils of Thymus caespititius from portugal Ligia R. Salgueiro, Roser Vila, Felix Tomi, A. Cristina Figueiredo, Jos¨¦G. Barroso, Salvador Cañigueral, Joseph Casanova, Ant¨®nio Proença da Cunha, Tom¨¤s Adzet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . compound 15 C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 1997 45 353-363 Sesqui- and diterpenoids from the japanese liverwort Jungermannia hattoriana Fumihiro Nagashima, Hironao Tanaka, Shigeru Takaoka, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . compound 36 ÏàËÆ¶È:53.3% Journal of Natural Products 1989 Vol 52 481 Preparation and Characterization of Naturally Occurring Longipinene Esters Pedro Joseph-Nathan, Carlos M. Cerda, Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . aristolone ÏàËÆ¶È:53.3% Journal of Natural Products 1993 Vol 56 921 Bioactive and Other Sesquiterpenoids from Porella cordeana G. G. Harrigan, A. Ahmad, N. Baj, T. E. Glass, A. A. L. Gunatilaka, D. G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . viridiflorol ÏàËÆ¶È:53.3% Phytochemistry 1996 42 677-679 (− -Ledol from the liverwort Cephaloziella recurvifolia and the clarification of its identityChia-Li Wu, Yu-Ming Huang, Jyh-Rong Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . 4-Eudesmene-1¦Â,11-diol C15H26O2 ÏàËÆ¶È:53.3% 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 -------------------------------------------------------------------------------- 51 . (1S,3R,4R,7S)-3,4-dihydroxy-¦Á-bisabolol. C15H28O3 ÏàËÆ¶È:53.3% Phytochemistry 1995 39 1077-1080 Biotransformation of (− -¦Á-bisabolol by plant pathogenic fungus, Glomerella cingulataMitsuo Miyazawa, Hirokazu Nankai, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . bisabolene-2,5-endoperoxide ÏàËÆ¶È:53.3% Korean Journal of Pharmacognosy 1993 24(2) 107-110 A New Endoperoxide from Artemisia selengensis Jang, Woo-Young; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 53 . Aristolone C15H22O ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 650-653 CHEMICAL CONSTITUENTS OF Chondrophycus papillosus AND THEIR CYTOTOXICITY IN VITRO Ling-Ling Sun, Chang-Yun Wang, Hao-Fu Dai,Chang-Lun Shao, Wen-Li Mei,Tao-Liu,and Ze-Dong Ma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 54 . 1-One-4-epi-alantolactone C15H20O3 ÏàËÆ¶È:53.3% Phytochemistry Letters 2012 5 229-232 Two new eudesmanolides from Inula racemosa and their bioactivities Ting Zhang, Ting Gong, Yan Yang, Ruo-Yun Chen , De-Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 55 . 4-epi-trans-dihydroagarofuran ÏàËÆ¶È:53.3% Magnetic Resonance in Chmesitry 2004 42 709-711 Dihydroagarofurans: the fourth isomer isolated from Cedrelopsis grevei bark oil Jean-François Cavalli, F¨¦lix Tomi, Antoine-François Bernardini and Joseph Casanova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 56 . Carabrone ÏàËÆ¶È:53.3% Archives of Pharmacal Research 2004 27 1029-1033 Phytochemical constituents of Carpesium macrocephalum FR- et SAV- Mi -Ran Kim, Seung -Kyu Lee, Chang -Soo Kim, Kyung -Soon Kim and Dong -Cheul Moon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 57 . compound 1b ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 1994 2039-2041 Synthesis of tridensone, a sesquiterpene ketone isolated from the liverwort Bazzania tridens. Structure revision and absolute configuration Motoo Tori, Kazuhiro Kosaka and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 58 . compound 1a ÏàËÆ¶È:53.3% Bulletin of the Chemical Society of Japan 1993 66 2694-2699 Synthetic Photochemistry. LXI. A Total Synthesis of (¡À)-Valeranone, a cis-Decalone Sesquiterpenoid from Valeriana officinalis, via an Intramolecular Photocycloaddition Hitoshi Takeshita, Ying-She Cui, Nobuo Kato, Akira Mori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 59 . arteannuin M C15H22O3 ÏàËÆ¶È:53.3% Tetrahedron 1998 54 4345-4356 A novel endoperoxide and related sesquiterpenes from Artemisia annua which are possibly derived from allylic hydroperoxides Lai-King Sy, Geoffrey D. Brown, Richard Haynes Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 60 . compound 22 C15H24O4 ÏàËÆ¶È:53.3% Tetrahedron 2001 57 8481-8493 Structure elucidation of arteannuin O, a novel cadinane diol from Artemisia annua, and the synthesis of arteannuins K, L, M and O Lai-King Sy, Kung-Kai Cheung, Nian-Yong Zhu, Geoffrey D Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 61 . 7-epi-ilicic acid C15H24O3 ÏàËÆ¶È:53.3% Tetrahedron 2000 56 Corrigendum to ¡°Jasonol, a Rare Tricyclic Eudesmane Sesquiterpene and Six other New Sesquiterpenoids from Jasonia candicans¡± Ahmed A Ahmed, Ahmed A Mahmoud Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2012-08-29 08:37:36
Ñî´óËÉ
ÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
- Ó¦Öú: 243 (´óѧÉú)
- ½ð±Ò: 23878.3
- É¢½ð: 3
- ºì»¨: 46
- Ìû×Ó: 10466
- ÔÚÏß: 831.8Сʱ
- ³æºÅ: 1190374
- ×¢²á: 2011-01-15
- רҵ: »¯Ñ§ÉúÎïѧÓëÉúÎïÓлú»¯Ñ§

4Â¥2012-08-29 14:07:16













»Ø¸´´ËÂ¥
-3-Bromomethyl-3-chloro-7-methyl-1, 6-octadiene from Sri Lankan Chondrococcus hornemanni