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»¯ºÏÎï1£º 1 . (3R,9R)-3,9-dihydroxymegastigm-5-en-4-one C13H22O3 ÏàËÆ¶È:81.2% Chemistry & Biodiversity 2007 Vol. 4 118 Phytotoxicity of Secondary Metabolites from Aptenia cordifolia Marina DellaGreca, Antonio Fiorentino, Angelina Izzo, Filomena Napoli, Raffaella Purcaro, and Armando Zarrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 69 C15H26O3 ÏàËÆ¶È:62.5% Heterocycles 2012 84 843-878 Development of an Intramolecular Gassman¡¯s [2+2] Cycloaddition John B. Feltenberger, Changhong Ko, Jun Deng, Sunil K. Ghosh, and Richard P. Hsung Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (4aS,6S,7S,8aS)-7-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-4a,5,6,7,8,8a-hexahydronaphthalen-2(1H)-one C15H24O3 ÏàËÆ¶È:62.5% Australian Journal of Chemistry 1984 37 629-633 New eudesmane sesquiterpenoids from Eremophila scoparia PJ Babidge and RA Massy-Westropp Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 9(E)-11-hydroxy-¦Á-santalol C15H24O2 ÏàËÆ¶È:56.2% 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 ̼Æ×Ä£Äâͼ 5 . 9(E)-11-hydroxy-¦Â-santalol C15H24O2 ÏàËÆ¶È:56.2% 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 ̼Æ×Ä£Äâͼ 6 . 9-hydroxy-3-epi-perforenone A C15H22O3 ÏàËÆ¶È:56.2% Journal of Natural Products 2003 66 435-437 Three New Sesquiterpenes from the Red Alga Laurencia perforata Anthony D. Wright, Eva Goclik, and Gabriele M. Knig Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (¡À)-epi-6-myoporol C15H24O3 ÏàËÆ¶È:56.2% Journal of Natural Products 1997 60 493-494 A Synthesis of 6-Myoporol Tse-Lok Ho and Rong-Jie Chein Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4¦Á-hydroxydihydroagarofuran C15H26O2 ÏàËÆ¶È:56.2% 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 9 . compound 20 C15H26O ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1987 35 124-135 Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae) ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (4R,4aR,8aR)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol C14H24O ÏàËÆ¶È:56.2% 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 11 . ((1S,4R,4aR,8aR)-4-isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)methanol C16H28O ÏàËÆ¶È:56.2% 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 12 . ¦Á-caissanol ÏàËÆ¶È:56.2% Phytochemistry 1985 24 2325-2328 Sesquiterpenes from carissa edulis Hans Achenbach, Reiner Waibel, Ivan Addae-Mensah Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . hexyl-6-(2,5-dioxopyrrolidin-1-yl)-2-(morpholin-4-yl)hexanoate C20H34O5N2 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2010 18 8556-8565 Investigating the activity of 2-substituted alkyl-6-(2, 5-dioxopyrrolidin-1-yl)hexanoates as skin penetration enhancers Katerina Brychtova, Radka Opatrilova, Ivan Raich, Danuta S. Kalinowski, Lenka Dvorakova, Lukas Placek, Jozef Csollei, Des R. Richardson, Josef Jampilek Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (6R or 6S)-7,7-dimethyl-11-methylenespiro[5.5]undec-2-ene-3-methanol C15H24O ÏàËÆ¶È:56.2% Helvetica Chimica Acta 2011 94 2295-2302 New and Bioactive Sesquiterpenes from Schisandra sphenanthera (pages 2295¨C2302) Khongorzul Mendbayar, I-Wen Lo, Chia-Ching Liaw, Yu-Chi Lin, Ahmed E. Fazary, Yuh-Chi Kuo, Hsiu-Ju Wang, Been Huang Chiang, Shorong-Shii Liou and Ya-Ching Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3,7,7-trimethyl-11-methylenespiro[5.5]undec-2-ene ÏàËÆ¶È:56.2% Russian Journal of Organic Chemistry 2001 37 362-374 Acid-Catalyzed Rearrangements of (-)-Thujopsene O. I. Yarovaya, M. P. Polovinka, D. V. Korchagina, Yu. V. Gatilov and I. Yu. Bagryanskaya, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (2R,4R)-octane-2,4-diol and (2R,4S)-octane-2,4-diol ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 2010 4785-4801 Conversion of Conjugated Enones into Enantiomerically Pure -Hydroxy Ketones or 1,3-Diols ¨C Samarium(II) Bromide Reductions of Protected ,-Dihydroxy Ketones Andreas Zörb and Reinhard Br¨¹ckner Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (1SR,7RS)-6,6,9-Trimethylbicyclo[5.4.0]undec-8-en-2-one C14H22O ÏàËÆ¶È:56.2% Tetrahedron 2012 68 5102-5108 A diastereoselective synthesis of (1SR,3SR,7RS)-3-methyl-¦Á-himachalene, the sex pheromone of the sandfly, Lutzomyia longipalpis (Diptera: Psychodidae) Samuel Dufour, Pascalie Castets, John A. Pickett, Antony M. Hooper Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (S)-(-)-3-(6-Hydroxytridec-3-yn-1-yl)-2,4,10-trioxatricycl0[3.3.1.1(3,7)]decane C20H32O4 ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 1995 1995 673-676 Synthesis of (4E,7S)-(− -7-Methoxy-4-tetradecenoic Acid, a Major Constituent of the Marine Cyanophyte Lyngbya MajusculaClaudia M¨¹ller, Gundula Voss and Hans Gerlach Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 20 C15H24O ÏàËÆ¶È:56.2% Journal of the Brazilian Chemical Society 2000 11 502-511 Synthesis of (¡À)-Africanol Francisco de A. Marques, Jo¨¦ T. B. Ferreira and Edward Piers Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 17¦Â-Acetylaminoestr-4-en-3-one ÏàËÆ¶È:55% Steroids 1998 63 484-495 Microbial hydroxylation of acetylaminosteroids HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2£º 1 . vittatalactone C16H30O2 ÏàËÆ¶È:68.7% Journal of Natural Products 2005 68 26-30 Vittatalactone, a ¦Â-Lactone from the Striped Cucumber Beetle, Acalymma vittatum Bruce D. Morris, Rebecca R. Smyth, Stephen P. Foster, Michael P.Hoffmann, Wendell L. Roelofs, Stephan Franke, and Wittko Francke Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 14-hydroxy-dauc-4-ene C15H26O ÏàËÆ¶È:68.7% Phytochemistry 1999 50 109-112 Sesquiterpene coumarins and sesquiterpenes from Ferula sinaica Ahmed A. Ahmed Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-vittatalactone C16H30O2 ÏàËÆ¶È:68.7% European Journal of Organic Chemistry 2011 4603-4608 Enantioselective Total Synthesis of (+)-Vittatalactone Jhillu S. Yadav, Nagendra Nath Yadav, T. Srinivasa Rao, B. V. Subba Reddy and Ahmad Al Khazim Al Ghamdi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N-methoxy-4-aza-5¦Â-cholestan-3-one ÏàËÆ¶È:63.1% Canadian Journal of Chemistry 1997 75 857-872 Thermolysis and photolysis of two steroidal hydroxamic acid methanesulfonates Oliver E. Edwards, Gunnar Grue-Sørensen, Barbara A. Blackwell Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 15-hydroxy-¦Á-cadinol C15H26O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2002 65 25-28 Five New Cadinane-Type Sesquiterpenes from the Heartwood of Chamaecyparis obtusa var. formosana Yueh-Hsiung Kuo, Chia-Hsien Chen,Shih-Chang Chien, and Yun-Lian Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Vulgarone B ÏàËÆ¶È:62.5% Natural Product Sciences 2009 15 229-233 In Vitro Anti-Inflammatory Effects of the Essential Oil of Artemisia iwayomogi and Its Main Component, Vulgarone B Chung, Eun-Young; Shin, Seung-Won Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . comopund 11 ÏàËÆ¶È:62.5% Phytochemistry 1989 28 2717-2721 Sesquiterpenoids and phenolics of Pulicaria paludosa Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,Jos¨¦ M. Miguel del Corral Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Vulgarone B C15H22O ÏàËÆ¶È:62.5% Archives of Pharmacal Research 2009 32 1711-1719 Antibacterial effects of vulgarone B from Artemisia iwayomogi alone and in combination with oxacillin Eun Young Chung, Youn Hee Byun, Eun Joo Shin, Ha Sook Chung and Yeon Hee Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 15 ÏàËÆ¶È:62.5% Journal of the Chemical Society, Perkin Transactions 1 2000 189-194 Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa Koon-Sin Ngo and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4¦Â-Hydroxyamorph-5-ene 15 and 4-hydroxyamorph-5-ene C15H26O ÏàËÆ¶È:62.5% Journal of the Chemical Society, Perkin Transactions 1 2000 189-194 Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa Koon-Sin Ngo and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 4¦Á-hydroperoxy-5-amorphene C15H26O2 ÏàËÆ¶È:62.5% Tetrahedron 1999 55 15109-15126 Autoxidation of 4-amorphen-11-ol and the biogenesis of nor- and seco-amorphane sesquiterpenes from fabiana imbricata Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-amorphene C15H26 ÏàËÆ¶È:62.5% Tetrahedron 1999 55 15109-15126 Autoxidation of 4-amorphen-11-ol and the biogenesis of nor- and seco-amorphane sesquiterpenes from fabiana imbricata Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 8-tert-butyl-3-isobutyl-1,4-dioxaspiro[4.5]decan-2-one ÏàËÆ¶È:62.5% Indian Journal of Chemistry 2012 51B 323-327 Iodine catalyzed protection of -hydroxy acids and its application for the synthesis of -hydroxy lactone Sharma, Chinta Mani; Kashyap, Bishwapran; Phukan, Prodeep Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (1R*,9aR*)-1-Hydroxy-1-methyl-3-[(Z)-2-methylpropylidene]perhydro-4-quinolizinone C14H23NO2 ÏàËÆ¶È:62.5% Journal of the Brazilian Chemical Society 2003 14 982-993 Studies Towards the Construction of Alkylidene Quinolizidines. The Total Synthesis of Homopumiliotoxin 223G Leonardo S. Santos and Ronaldo A. Pilli Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (1E,4R,4aR,5S,6R,8aR)-5.6-epoxy-4-isopropyl-6-methyl-3,4,4a,5,6,7,8,8a-octahydrontalene-1-methanol acetate C15H22O ÏàËÆ¶È:62.5% Australian Journal of Chemistry 1986 39 1717-1722 Studies of Australian Soft Corals. XXXIX. New Sesquiterpene Metabolites From Several Xenia Species (Xeniidae, Octocorallia, Anthozoa) BF Bowden, JC Coll and RH Willis Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . tiomanene C17H25BrO ÏàËÆ¶È:58.8% Phytochemistry 2008 69 2490-2494 Antibacterial activity of halogenated sesquiterpenes from Malaysian Laurencia spp. Charles Santhanaraju Vairappan, Minoru Suzuki,Takahiro Ishii, Tatsufumi Okino,Tsuyoshi Abe,Michio Masuda Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . maali-3-en-8¦Á-ol C17H26O2 ÏàËÆ¶È:58.8% Phytochemistry 2002 59 39-44 Microbial metabolism of partheniol by Mucor circinelloides Galal T. Maatooq Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 1¦Â-Acetoxy-3-eudesmen-11-ol C17H28O3 ÏàËÆ¶È:58.8% 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 19 . intrlcatetraol diacetate C34H58Br2Cl2O8 ÏàËÆ¶È:58.8% Phytochemistry 1993 33 651-656 Intricatetraol, a halogenated triterpene alcohol from the red alga Laurencia intricata Minoru Suzuki, Yoshihide Matsuo, Satoshi Takeda, Teruaki Suzuki Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (E)-and(Z)-N-(3-methylcyclohexylidene)-1-propanamine ÏàËÆ¶È:58.8% Journal of Heterocyclic Chemistry 2000 37 1309-1314 Convenient one-pot syntheses of pyrazoles from imines, a vilsmeier type reagent and hydrazine Alan R. Katritzky, Anna Denisenko, Sergey N. Denisenko and Michael Arend Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (18E)-(20S)-18-(hydroxyimino)-des-A,B-cholestan-8¦Â-ol C18H33NO2 ÏàËÆ¶È:58.8% Bioorganic & Medicinal Chemistry 2009 17 7658-7669 Removal of the 20-methyl group from 2-methylene-19-nor-(20S)-1¦Á,25-dihydroxyvitamin D3 (2MD) selectively eliminates bone calcium mobilization activity Rafal Barycki, Rafal R. Sicinski, Lori A. Plum, Pawel Grzywacz, Margaret Clagett-Dame, Hector F. DeLuca Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (3S,3aS,6R,7R,9aS)-N-(6-hydroxy-1,1,7-trimethyldecahydro-3a,7-methanocyclopentacyclooct-3-yl)acetamide C17H29NO2 ÏàËÆ¶È:58.8% Russian Journal of Organic Chemistry 2004 40 1593-1598 Reactions of caryophyllene, isocaryophyllene, and their epoxy derivatives with acetonitrile under ritter reaction conditions O. I. Yarovaya, D. V. Korchagina, T. V. Rybalova, Yu. V. Gatilov and M. P. Polovinka, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |

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-7-Methoxy-4-tetradecenoic Acid, a Major Constituent of the Marine Cyanophyte Lyngbya Majuscula