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341176
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- Ó¦Öú: 30 (СѧÉú)
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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2015-05-16 00:25:44
gengwenyue: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-01 11:10:49
À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2015-05-16 00:25:44
gengwenyue: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-01 11:10:49
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1 . (1aS,3R,4R,4aR,6S,7R,8aS)-7-chloro-3,6-dihydroxy-3,4a,8,8-tetra-methyl-octahydro-1aH-naphtho[1-b]oxirene-4-carboxylic acid C15H23ClO5 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2005 2005 5100-5105 Novel Highly Substituted Biraryl Ethers, Phomosines D¨CG, Isolated from the Endophytic Fungus Phomopsis sp. from Adenocarpus foliolosus Jingqiu Dai, Karsten Krohn, Ulrich Flörke, Dietmar Gehle, Hans-J¨¹rgen Aust, Siegfried Draeger, Barbara Schulz and Joachim Rheinheimer Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cadinane-4¦Â,5¦Á,10¦Â-triol C15H28O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (11S)-1¦Â,4¦Á,6¦Â,11,12-pentahydroxyeudesmane C15H28O5 ÏàËÆ¶È:60% Journal of Natural Products 2002 65 1011-1015 Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Andr¨¦s Parra, and Francisco Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (4Z,8¦Á,11S)-caryophyll-4(5)-ene-8,14-diol C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2000 63 44-47 Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4¦Â,5¦Á, 10¦Â-trihydroxycadinane C15H26O2 ÏàËÆ¶È:60% Planta Medica 1997 63 250-254 Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti) Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 4 C15H26O ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1990 38 1405-1407 Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. IV Hisakatsu IWABUCHI,Nobuo KATO and Masahiro YOSHIKURA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Thunaloside hexaacetate C27H36O15 ÏàËÆ¶È:60% Phytochemistry 1994 35 1259-1261 Alatoside and thunaloside, two iridoid glucosides from Thunbergia alata Søren Damtoft, Lotte Boe Frederiksen, Søren Rosendal Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1aS,2S,6aS,6bS,7S)-7-tert-Butoxy-4,4-dimethyl-3,5-dioxa-2-mesyloxymethylpyrrolidino[1,2-b]isoxazolidino-[4,5]cycloheptane C17H31NO7S ÏàËÆ¶È:60% Canadian Journal of Chemistry 2006 84 534-539 Synthesis of 8-homocastanospermine1 Konrad Pa niczek, Dariusz Socha, Margarita Jurczak, Jolanta Solecka, and Marek Chmielewski Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1¦Â-hydroxycolartin C15H24O4 ÏàËÆ¶È:60% China Pharmacy 2012 23 2549-2550 Study on Chemical Constituents in Chloroform Part of Inula racemosa GAO Ni, GONG You-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Trefolane A C15H26O2 ÏàËÆ¶È:60% Organic Letters 2012 14 4976-4978 Trefolane A, a Sesquiterpenoid with a New Skeleton from Cultures of the Basidiomycete Tremella foliacea Jian-Hai Ding, Tao Feng, Zheng-Hui Li, Xiao-Yan Yang, Hua Guo, Xia Yin, Gang-Qiang Wang, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 5-(¦Â-D-glucopyranosyloxy)-2-(3-hydroxybutyl)-1,3,3-trimethylcyclohexene C19H34O7 ÏàËÆ¶È:58.8% Journal of Natural Products 1993 Vol 56 2142 Coumarins and Other Constituents of Prunus prostrata A. R. Bilia, C. Cecchini, A. Marsili, I. Morelli, S. Mele Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . avrainvilloside C45H87NO9 ÏàËÆ¶È:57.1% Journal of Natural Products 2005 68 1428-1430 Avrainvilloside, a 6-Deoxy-6-aminoglucoglycerolipid from the Green Alga Avrainvillea nigricans Raymond J. Andersen, and Orazio Taglialatela-Scafati Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . megastigm-5-en-3,9-diol ÏàËÆ¶È:57.1% Phytochemistry 1999 51 793-801 Terpenes and lignans from leaves of Chamaecyparis formosensis Tung-Chieh Lin, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (10R*)-10-O-methylfurocaespitanelactol C13H18BrClO3 ÏàËÆ¶È:57.1% Journal of Natural Products 2010 73 27-32 Cytotoxic Halogenated Metabolites from the Brazilian Red Alga Laurencia catarinensis Cintia Lhullier, Miriam Falkenberg, Efstathia Ioannou, Antonio Quesada, Panagiota Papazafiri, Paulo Antunes Horta, Eloir Paulo Schenkel, Constantinos Vagias and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (10S*)-10-O-methylfurocaespitanelactol C13H18BrClO3 ÏàËÆ¶È:57.1% Journal of Natural Products 2010 73 27-32 Cytotoxic Halogenated Metabolites from the Brazilian Red Alga Laurencia catarinensis Cintia Lhullier, Miriam Falkenberg, Efstathia Ioannou, Antonio Quesada, Panagiota Papazafiri, Paulo Antunes Horta, Eloir Paulo Schenkel, Constantinos Vagias and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . teuhetenone A ÏàËÆ¶È:57.1% Phytochemistry 1995 39 617-619 Nor-sesquiterpenes from Teucrium heterophyllum Braulio M. Fraga, Melchor G. Hern¨¢ndez, Teresa Mestres, David Terrero, Jos¨¦M. Arteaga Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . teuhetenone A C12H18O32 ÏàËÆ¶È:57.1% Zeitschrift f¨¹r Naturforschung B 2007 62b 125-128 Jasonone, a Nor-sesquiterepene from Jasonia montana Abou El-Hamd H. Mohamed Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 1 C12H17LiN2NaO7PS ÏàËÆ¶È:57.1% Organic letters 1999 1 99-102 Synthesis of a Reaction Intermediate Analogue of Biotin-Dependent Carboxylases via a Selective Derivatization of Biotin David R. Amspacher, Carol Z. Blanchard, Frank R. Fronczek, Marcelo C. Saraiva, Grover L. Waldrop, and Robert M. Strongin Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 1-O-L-valyl-D-mannitol ÏàËÆ¶È:57.1% Indian Journal of Chemistry Section B 2007 46B 2026-2044 Enzymatic syntheses of L-valyl,L-leucyl and L-isoleucyl esters of carbohydrates using Candida rugosa lipase Somashekar,Bhandya R; Divakar,Soundar Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-05-15 20:32:20
gengwenyue
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