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²éѯ½á¹û£º¹²²éµ½154¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (1R,10R)-9¦Â-hydroxyaromadendrane C15H26O ÏàËÆ¶È:66.6% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (1S,10S)-9¦Á-hydroxy-allo-aromadendrane C15H26O ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . [1RS,2RS,5E,9SR,10RS]-1,5,8,8-tetramethylbicyclo[8.1.0]undec-5-ene-2,9-diol C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 1441-1442 A Stable Rearrangement Product of Humulene-4,5-epoxide Raymond M. Carman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 11-Hydroxy-4,5-secoeudesmane-4,5-dione ÏàËÆ¶È:60% Phytochemistry 1995 39 603-607 Sesquiterpenes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (1R,4R,9S)-5-hydroxy-caryophyll-3Z-en-14-al C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1990 29 757-763 Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . [(1R,2R,5R)-1-allyl-2-isopropyl-5-methylcyclopentyl]methanol C13H24O ÏàËÆ¶È:60% European Journal of Organic Chemistry 2011 5167-5175 Enantioselective Synthesis of the Unnatural Enantiomers of the Fungal Sesquiterpenoids Acorenone and Trichoacorenol Nelson L. Brock and Jeroen S. Dickschat Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . N,N,N-Trimethyl-3-(2-(2-octanoyloxazol-5-yl)ethylsulfonyl)propan-1-ammonium iodide C19H35N2O4S ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2012 20 1100-1112 Design, synthesis and evaluation of polar head group containing 2-keto-oxazole inhibitors of FAAH Marion Rusch,Stefan Zahov,Ingrid R. Vetter, Matthias Lehr, Christian Hedberg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (+)-2-[(1S,2S,4aS,8aR)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]ethanol ÏàËÆ¶È:56.2% Helvetica Chimica Acta 2014 97 197-214 Enantioselective Access to (− -Ambrox® Starting from ¦Â-FarneseneChristian Chapuis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2 C20H30O ÏàËÆ¶È:55% Journal of Natural Products 2006 69 1411-1416 Cytotoxic Constituents from the Formosan Soft Coral Clavularia inflata var. luzoniana Shang-Kwei Wang, Min-Jay Huang, and Chang-Yih Duh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (10¦Â)-10-Hydroxyaristolan-9-one C15H24O2 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2007 Vol. 90 385 Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red Alga Laurencia similis (Rhodomelaceae) Nai-Yun Ji, Xiao-Ming Li, Lan-Ping Ding, and Bin-Gui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 4-Epicurcumenol C15H22O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2001 49(12) 1558-1566 Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 1a ,10a -dihydro-derivative ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2001 49(12) 1558-1566 Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . drimenal C15H24O ÏàËÆ¶È:53.3% Phytochemistry 2004 65 2583-2588 Bioactivity guided isolation of antifungal compounds from the liverwort Bazzania trilobata (L.) S.F. Gray Jochen M. Scher, John-Bryan Speakman, Josef Zapp, Hans Becker Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (1R,10R)-aromadendran-9-one C15H24O ÏàËÆ¶È:53.3% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (1R,10R)-13-hydroxyaromadendr-9-one C15H24O2 ÏàËÆ¶È:53.3% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-(1S,6S,9R)-4-acetyl-1-hydroxy-6-isopropyl-9-methylbicyclo[4.3.0]non-4-en-3-one C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2006 69 1261-1266 Minor Sesquiterpenes with New Carbon Skeletons from the Brown Alga Dictyopteris divaricata Fuhang Song, Xiuli Xu, Shuai Li, Sujuan Wang, Jielu Zhao,Yongchun Yang, Xiao Fan, Jiangong Shi, and Lan He Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 2a C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 31-36 Africane-Type Sesquiterpenoids from the Argentine Liverwort Porella swartziana and Their Antibacterial Activity Graciela Bovi Mitre, Norma Kamiya, Alicia Bardn, and Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . (-)-(1R,6S,7S,10R)-1-hydroxycadinan-3-en-5-one C15H24O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 1644-1649 Cadinane Sesquiterpenes from the Brown Alga Dictyopteris divaricata Fuhang Song, Xiao Fan, Xiuli Xu, Jielu Zhao, Yongchun Yang, and Jiangong Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . silphinen-3,5-dione C15H20O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 448-453 C-5-Substituted Antifeedant Silphinene Sesquiterpenes from Senecio palmensis Mat¨ªas Reina, Matthias Nold, Omar Santana,Juan Carlos Orihuela, and Azucena Gonz¨¢lez-Coloma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . mirabilin B C15H23N3 ÏàËÆ¶È:53.3% Journal of Natural Products 1997 60 704-707 Three New Tricyclic Guanidine Alkaloids from the Sponge Batzella sp. Ashok D. Patil, Alan J. Freyer, Priscilla Offen, Mark F. Bean, and Randall K. Johnson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 16 ÏàËÆ¶È:53.3% Journal of Natural Products 1997 60 1026-1030 Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens) Alejandro F. Barrero, Pilar Arteaga, Jos¨¦F. Qu¨ªlez, Ignacio Rodr¨ªguez, and M. Mar Herrador Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . compound 1 ÏàËÆ¶È:53.3% Phytochemistry 2000 55 749-753 The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . tricyclo[5,3,1,0(2,4)]-3-aldehyde-3,11-dimethyl-8-methanoic acid C15H22O3 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2008 44 308-310 A NOVEL SESQUITERPENOID FROM Ecdysanthera rosea Fu-Quan Xu, Hai-Yang Liu,Chang-Xiang Chen, and Hui-Min Zhong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . aristolan-10-ol-9-one C15H24O2 ÏàËÆ¶È:53.3% Chinese Chemical Letters 2007 18 178-180 Two new aristolane sesquiterpenes from Laurencia similis Nai Yun Ji, Xiao Ming Li, Lan Ping Ding, Bin Gui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . 3-(1',2',2'-Trimethyl-6'-oxo-1'-cyclohexyl)propionsaure-methylester C13H22O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 1980 63 1833-1855 Photochemische Reaktionen 111. Mitteilung [1] Zur Photochemie , -ungesättigter , -Epoxyester I: Singulett- versus Triplettreaktivität Alex Peter Alder, Hans Richard Wolf, Oskar Jeger Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . 10-Hydroxyaristolan-9-one C15H24O2 ÏàËÆ¶È:53.3% Molecules 2009 14 1889-1897 Sesquiterpenes from Laurencia similis Hua Su, Da-Yong Shi, Jing Li, Shu-Ju Guo, Li-Li Li, Zhao-Hui Yuan and Xiao-Bin Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . Aristolan-9-en-1-one C15H22O ÏàËÆ¶È:53.3% Molecules 2009 14 1889-1897 Sesquiterpenes from Laurencia similis Hua Su, Da-Yong Shi, Jing Li, Shu-Ju Guo, Li-Li Li, Zhao-Hui Yuan and Xiao-Bin Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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