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Òäʧ345: ½ð±Ò+8, ¡ïÓаïÖú 2015-02-07 21:04:00
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Òäʧ345: ½ð±Ò+8, ¡ïÓаïÖú 2015-02-07 21:04:00
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1 . 10¦Á-Hydroxyl-artemisinic acid C15H22O3 ÏàËÆ¶È:93.3% Natural Product Communications 2010 5 1531 - 1534 A New Sesquiterpene and other Constituents fromSaussurea lappa Root Jin-ao Duan*, Pengfei Hou, Yuping Tang, Pei Liu, Shulan Su and Hanqing Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 5a,9-dimethyl-3-methylene-3,3a,4,5,5a,6,7,8-octahydro-1-oxacyclopenta[c]azulen-2-one C15H20O2 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2006 54(8) 1187-1189 Two New Sesquiterpene Lactones from the Leaves of Laurus nobilis Stefano DALL¡¯ACQUA,Giampietro VIOLA,Michela GIORGETTI,Maria Cecilia LOI,and Gabbriella INNOCENTI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (5E,9E,13R)-13,14-Dihyduoxy-6,10,14-trimethyentadeca-5,9-dien-2-one C18H30O2 ÏàËÆ¶È:64.7% Australian Journal of Chemistry 1982 35 171-182 C18 terpenoid metabolites of the brown alga Cystophora moniliformis BN Ravi, PT Murphy, RO Lidgard, RG Warren and RJ Wells Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5,9,9-Trimerhylspiro[3.6]deca- 5.7-dien-1-one C13H18O ÏàËÆ¶È:64.2% Helvetica Chimica Acta 1981 64 2598-2605 Photochemical Reactions. 125th communication [1]. Photochemistry of homoconjugated cyclobutanones. I. Synthesis and photolysis of a Spiro [3.6]deca-5, 7-dien-1-one Terry A. Lyle, Bruno Frei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-Cumacrene, (4S)-4-[(1R,2S)-2-isopropenyl-1-methylcyclobutyl]-1-methylcyclohexene C15H24 ÏàËÆ¶È:60% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-Cumacrene, (4S)-4-[(1R,2S)-2-isopropenyl-1-methylcyclobutyl]-1-methylcyclohexene C15H24 ÏàËÆ¶È:60% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 9(E)-11-hydroxy-¦Â-santalol C15H24O2 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 1805-1808 Bisabolane- and Santalane-Type Sesquiterpenoids from Santalum album of Indian Origin Tae Hoon Kim, Hideyuki Ito, Tsutomu Hatano, Toshio Hasegawa,Aiko Akiba, Takahisa Machiguchi, and Takashi Yoshida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Neroplomacrol C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2010 73 563-567 Sesquiterpenes from Oplopanax horridus Taichi Inui, Yuehong Wang, Dejan Nikolic, David C. Smith, Scott G. Franzblau and Guido F. Pauli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (¡À)-cis-nerolidol ÏàËÆ¶È:60% Phytochemistry 1995 40 1133-1137 Biotransformations of acyclic terpenoids, (¡À)-cis-nerolidol and nerylacetone, by plant pathogenic fungus, Glomerella cingulata Mitsuo Miyazawa, Hirokazu Nankai, Hiromu Kameoka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-Amorphen-11-ol C15H26O ÏàËÆ¶È:60% Phytochemistry 1994 35 425-433 The sesquiterpenes of Fabiana imbricata Geoffrey D. Brown Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-(2-Oxo-2-piperidin-1-ylethyl)isoindolin-1-one C15H18N2O2 ÏàËÆ¶È:60% Canadian Journal of Chemistry 2005 83 990-1005 Synthesis of N-substituted isoindolinones via a palladium catalysed three-component carbonylation - amination - Michael addition cascade1 Ronald Grigg, Xinjie Gai, Tossapol Khamnaen, Shuleewan Rajviroongit,Visuvanathar Sridharan, Lixin Zhang, Simon Collard, and Ann Keep Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (Z)-nerolidol ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Á-¶ÅËÉÏ© ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2006 37 995+1037 ÏãÁÛëާ»¯Ñ§³É·ÖµÄÑо¿(¢ò) ÉòÖ¾±õ;ÕÅά¿â;ÂíÓ¢Àö;Ò¶ÎIJŠStructure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 22 ÏàËÆ¶È:60% Tetrahedron Letters 2002 43 3337-3340 An unexpected retro-aldol¨Caldol in the AB-ring in the synthesis of (¡À)-arisugacin A Jiashi Wang, Kevin P. Cole, Lin-Li Wei, Luke R. Zehnder, Richard P. Hsung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (+)-¦Á-amuurolene ÏàËÆ¶È:60% Natural Product Research and Development 2003 15 199-202 STUDIES ON THE CHEMICAL CONSTITUENTS OF MARINE SPONGE ACANTHELLASP.FROM THE SOUTH CHINA SEA YAN Xiao-hong; SONG Guo-qiang; ZHOU Xiu-hong; LIU Song-bai; GUO Yue-wei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (3S,6E,10R)-3,10,11-trihydroxy-3,7,11-trimethyldodeca-1,6-diene C15H28O3 ÏàËÆ¶È:60% Tetrahedron 2006 62 8952-8958 Unusual sesquiterpene glucosides from Amaranthus retroflexus Antonio Fiorentino, Marina DellaGreca, Brigida D'Abrosca, Annunziata Golino, Severina Pacifico, Angelina Izzo, Pietro Monaco Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 4-amorphen-11-ol ÏàËÆ¶È:60% Tetrahedron 1999 55 15099-15108 Synthesis of amorphane and cadinane sesquiterpenes from fabiana imbricata Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . (+)-¦Á-muurolene ÏàËÆ¶È:60% Tetrahedron 1996 52 2359-2368 Terpenoids with antifouling activity against barnacle larvae from the marine sponge Acanthella cavernosa Hiroshi Hirota, Yasuhiko Tomono, Nobuhiro Fusetani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (4R,4aS,8aR)-3,4,4a,7,8,8a-hexahydro-4-isopropyl-1,6-dimethylnaphthalene ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2004 40 337-345 Functionalization of the Allyl Fragment in (+)-¦Ä-Cadinol F. A. Valeev, I. P. Tsypysheva, A. M. Kunakova, O. Yu. Krasnoslobodtseva and O. V. Shitikova, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (3R,6E,10S)-2,6,10-trimethyl-3-hydroxydodeca-6,11-diene-2,10-diol ÏàËÆ¶È:60% Journal of Chemical Ecology 2009 35 39-49 Megalanthine, a Bioactive Sesquiterpenoid from Heliotropium megalanthum , its Degradation Products and their Bioactivities Francisco A. Mac¨ªas, Ana M. Simonet, Brigida D¡¯Abrosca, Claudia C. Maya and Mat¨ªas Reina, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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