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ÕâÊÇÄãÇóÖúµÄ»¯ºÏÎïÔÚÏàËÆ¶È50%ÒÔÉÏµÄÆ¥ÅäÐÅÏ¢ ²éѯ½á¹û£º¹²²éµ½25¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-(1,1-dimethylethyl)-2-[2-(1H-1,2,4-triazol-1-yl)ethyl]-1,3-benzodioxole C15H19N3O2 ÏàËÆ¶È:61.5% European Journal of Organic Chemistry 2011 1985-1992 Synthesis of all-syn Functionalized Triphenylene Ketals Nader M. Boshta, Martin Bomkamp, Gregor Schnakenburg and Siegfried R. Waldvogel Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-bisabolene ÏàËÆ¶È:60% Phytochemistry 1983 22 1040-1042 Helianthol a, a sesquiterpene alcohol from Helianthus tuberosus Mitsuo Miyazawa, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-(2',2'-Dimethyl-6'-methylidencyclohept-1'-yliden)-2-butanon C14H22O ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1980 63 1520-1537 Photochemische Reaktionen. 110. Mitteilung [1]. Zur Photochemie ,-Methano--enone Keitaro Ishii, Hans Richard Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . furocaespitane ÏàËÆ¶È:53.8% Tetrahedron letters 1979 20 2719-2722 Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes A.G. Gonz¨¢lez, J.D. Mart¨ªn, V.S. Mart¨ªn, M. Norte Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . A-Ligand C14H26N8 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2012 20 3470-3479 Synthesis and binding properties of new selective ligands for the nucleobase opposite the AP site Original Research Article Yukiko Abe, Osamu Nakagawa, Rie Yamaguchi, Shigeki Sasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-[(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)(phenyl)methyl]-5,5-dimethylcyclohexane-1,3-dione ÏàËÆ¶È:53.8% Helvetica Chimica Acta 2011 94 1943-1951 Facile Knoevenagel and Domino Knoevenagel/Michael Reactions Using Gel-Entrapped Base Catalysts (pages 1943¨C1951) Shital Shinde, Gajanan Rashinkar, Arjun Kumbhar, Santosh Kamble and Rajashri Salunkhe Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 13 C15H24O3 ÏàËÆ¶È:53.3% Phytochemistry 1992 31 143-147 Biotransformation of sesquiterpenes by cultured cells ofCurcuma zedoaria Norihiro Sakui, Masanori Kuroyanagi, Yoko Ishitobi, Makoto Sato, Akira Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 21 C15H20O3 ÏàËÆ¶È:53.3% Phytochemistry 1991 30 899-904 Eremophilanes and furoeremophilanes from Euryops jacksonii and E. Algoensis P. Gonser, J. Jakupovic, G.M. Mungai Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 5c C16H20N2OS ÏàËÆ¶È:53.3% Tetrahedron Letters 2012 53 762-764 Stereoselective synthesis of novel annulated thiopyrano indole derivatives from simple oxindole via intramolecular 1,3-dipolar cycloaddition reactions of nitrone and nitrile oxide Swarup Majumder,Pulak J. Bhuyan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Moskachan D ÏàËÆ¶È:53.3% Phytochemistry 1986 25 2209-2210 Four aromatic derivatives from Ruta angustifolia J. Borges Del Castillo, M. Secundino, F. Rodr¨ªguez Luis Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . chokol B C15H26O2 ÏàËÆ¶È:53.3% Agricultural and Biological Chemistry 1989 53 789-796 New Fungitoxic Sesquiterpenoids, Chokols A-G, from Stromata of Epichloe typhina and the Absolute Configuration of Chokol E Hiroyuki KOSHINO, Satoshi TOGIYA, Shun-ichi TERADA, Teruhiko YOSHIHARA, Sadao SAKAMURA, Tadayuki SHIMANUKI, Tohru SATO, Akitoshi TAJIMI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . purealidin A C17H24Br2N6O3 ÏàËÆ¶È:53.3% Tetrahedron 2012 68 9802-9807 Structural and stereochemical investigations into bromotyrosine-derived metabolites from southern Australian marine sponges, Pseudoceratina spp. Angela A. Salim, Zeinab G. Khalil, Robert J. Capon Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-(1'',1''-Dimethylprop-2-enyl)-2-(3'-methylbut-2'-enyl)phenol C16H22O ÏàËÆ¶È:53.3% Australian Journal of Chemistry 1979 32 2783-2786 A New Phenol from the Brown Alga Perithalia caudata Containing a 'Reverse' Isoprene Unit at the 4-Position AJ Blackman, C Dragar and RJ Wells Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Compound 6b C20H26N2OS ÏàËÆ¶È:52.9% Tetrahedron Letters 2012 53 762-764 Stereoselective synthesis of novel annulated thiopyrano indole derivatives from simple oxindole via intramolecular 1,3-dipolar cycloaddition reactions of nitrone and nitrile oxide Swarup Majumder,Pulak J. Bhuyan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (E)-¦Ã-Macrocarpene, (1E)-3',3',4-trimethyl-1,1'-bi(cyclohexane)-1(1'),3-diene C15H24 ÏàËÆ¶È:50% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â,12-dihydroxy-13-methylpodocarpane-8,10,13-triene C18H26O2 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2004 52(5) 608-611 New Lathyrane and Podocarpane Diterpenoids from Jatropha curcas Nasi RAVINDRANATH, Majjigapu RAVINDER REDDY, Chimmani RAMESH, Ravirala RAMU, Anabathula PRABHAKAR, Bharatam JAGADEESH, and Biswanath DAS Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 11-hydroxy-4-oxo-tetradecanoic acid C14H26O4 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 487-492 Ipomoeassins A−E, Cytotoxic Macrocyclic Glycoresins from the Leaves of Ipomoea squamosa from the Suriname Rainforest Shugeng Cao, Rebecca C. Guza, Jan H. Wisse, James S. Miller, Randy Evans, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3,7-dihydroxycymopolone C16H21O4Br ÏàËÆ¶È:50% Journal of Natural Products 2002 65 329-333 New Prenylated Bromoquinols from the Green Alga Cymopolia barbata Enrique Dorta,Jos¨¦ Darias, Aurelio San Mart¨ªn, and Mercedes Cueto Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2-(3-Hydrony-3-methylbutyl),4-(3-methylbut-2-enyl) phenol C16H24O2 ÏàËÆ¶È:50% Phytochemistry 1993 34 107-111 Secondary metabolite chemistry of the Australian brown alga Encyothalia cliftonii: Evidence for herbivore chemical defence Vassilios Roussis, Rachel L. King, William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2-(7-(Dimethylamino)-2-oxo-2H-chromen-4-yl)-N-(prop-2-ynyl)-acetamide C16H16N2O3 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 1659-1666 An Optimized Immunoaffinity Fluorescent Method for Natural Product Target Elucidation Wei-luen Yu, Gianni Guizzunti, Timothy L. Foley, Michael D. Burkart, and James J. La Clair Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (1S,2S)-2-[(R)-1-Hydroxy-4-methylpentan-3-yl]-4-methylcyclohex-3-enecarboxylic Acid C14H24O3 ÏàËÆ¶È:50% Organic Letters 2010 Vol.12,No.5 904-907 Total Synthesis of 10-Isocyano-4-cadinene and Determination of Its Absolute Configuration Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata,Erina Yoshimura, Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (1S,2S)-2-((R)-1-hydroxy-4-methylpentan-3-yl)-4-methylcyclohex-3-enecarboxylic acid C14H24O3 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2011 76 6558-6573 Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 16 C14H20O ÏàËÆ¶È:50% Tetrahedron Letters 2005 46 8831-8835 A sequential RCM/fragmentation protocol towards chiral, stereodefined medium ring sesquiterpenoids. A carvone route to E- and Z-germacrenes Goverdhan Mehta, R. Senthil Kumaran Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3-(2'',3''-Epoxy-3''-methylbutyl)-2-(3'-hydroxy-3'-methylbutyl)indole ÏàËÆ¶È:50% European Journal of Organic Chemistry 1995 1995 1327-1337 Constituents of tropical medicinal plants, LXIX. The hexalobines, diprenylated indoles from Hexalobus crispiflorus and Hexalobus monopetalus Hans Achenbach, Christian Renner and Reiner Waibel Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 2-Acetonyl-6-isopropenyl-3-methyl-cycloheptenone ÏàËÆ¶È:50% Journal of the Brazilian Chemical Society 2001 12 154-158 A Novel Dihydroxy Nor-Guaiane Sesquiterpene: Synthesis and Crystal Structure Analysis. Julio Zukerman-Schpector, Ignez Caracelli, Cristina C. Carvalho, Mary L. de Faria, Fernando C. Silva, Luiz G. de O. Matias and Timothy J. Brocksom Structure 13C NMR ̼Æ×Ä£Äâͼ |
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