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164.1,123.7,66.6,49.5,45.6,39.8,37.2,34.8,28.2,27.6,27.3,25.8,24.8,23.2,22.3,21.1,12.6

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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 Majuscula
Claudia M¨¹ller, Gundula Voss and Hans Gerlach
Structure      13C NMR   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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