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1 .     ylangenol
Cl5H20O2     ÏàËÆ¶È:86.6%
Journal of Natural Products          1991          Vol 54          416
Sesquiterpenoids from Brachylaena hutchinsii
Paulo C. Vieira, Masaki Himejima, Isao Kubo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     15-copaenol
    ÏàËÆ¶È:86.6%
Phytochemistry          1988          27          1121-1123
Sesquiterpenoids from Pilgerodendron uv¨ªfera
M.Luisa Oyarz¨²n,Juan A. Garbarino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ¦Á-Copaene
    ÏàËÆ¶È:73.3%
Magnetic Resonance in Chmesitry          2001          39          621-624
Enantiomeric differentiation of terpenic olefins by carbon-13 NMR using chiral binuclear shift reagents
Nicolas Baldovini, F¨¦lix Tomi and Joseph Casanova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     15-copaenyl acetate
    ÏàËÆ¶È:70.5%
Phytochemistry          1988          27          1121-1123
Sesquiterpenoids from Pilgerodendron uv¨ªfera
M.Luisa Oyarz¨²n,Juan A. Garbarino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (1S,2S)-1,3,3-trimethyl-2-(3-oxobutyl)cyclohexyl acetate
C15H26O3     ÏàËÆ¶È:66.6%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     [(4aS,8aS)-3,4,4a,5,6,7,8,8a-Octahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]methyl Trifluoroacetate
    ÏàËÆ¶È:66.6%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     5¦Á-hydroxy-4(15)-eudesmene-1-one
C15H24O2     ÏàËÆ¶È:66.6%
Journal of Chemical Research          2008          32          520-521
Eudesmane-type sesquiterpenes from Senecio ambraceus
Xie, Wei Dong; Lai, Peng Xiang; Zhao, Hong; Row, Kyung Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     guai-2-en-10¦Á-ol
C15H26O     ÏàËÆ¶È:66.6%
European Journal of Medicinal Chemistry          2010          45          2237-2244
Guaiane sesquiterpenes from seaweed Ulva fasciata Delile and their antibacterial properties
Kajal Chakraborty, A.P. Lipton, R. Paulraj, Rekha D. Chakraborty
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     cubebol
    ÏàËÆ¶È:60%
Natural Product Research          1993          2          231-236
Aduncamide, a Cytotoxic and Antibacterial b-Phenylethylamine-Derived Amide from Piper aduncum
Jimmy Orjala; Anthony D. Wright; Topul Rali; Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (lR,5R,6R,8S)-dec[4.4.0]ane-1,5-dimethyl-8-( l'-methylethenyl)-5-isothiocyanate
C16H25SN     ÏàËÆ¶È:60%
Journal of Natural Products          1992          Vol 55          633
Two New Sesquiterpene Isothiocyanates from the Marine Sponge Acanthella klethra
Gabriele M. König, Anthony D. Wright, Otto Sticher, Frank R. Fronczek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     4-epi-cubebol
C15H26O     ÏàËÆ¶È:60%
Phytochemistry          1994          37          1327-1330
Sesquiterpenes from the brown alga Taonia atomaria
Salvatore De Rosa, Alfonso De Giulio, Carmine Iodice, Nevenka Zavodink
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     cubebol
C15H26O     ÏàËÆ¶È:60%
Phytochemistry          1994          37          1327-1330
Sesquiterpenes from the brown alga Taonia atomaria
Salvatore De Rosa, Alfonso De Giulio, Carmine Iodice, Nevenka Zavodink
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     capsidiol
C15H24O3     ÏàËÆ¶È:60%
Phytochemistry          1993          33          787-789
Evidence for the metabolism of capsidiol by a cytochrome P-450-dependent enzyme
Isabelle Saimmaime, Philippe J. Coulomb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     2,2,6¦Á,7¦Â-tetramethyl-bicyclo[4.3.0]non-9(1)-en-7¦Á-ol
C13H22O     ÏàËÆ¶È:60%
Helvetica Chimica Acta          1976          59          32-75
Verbindungen der 3,4-Dihydrojonon-Reihe als Modelle zur Photochemie y, 6-bzw. 6, e-ungesattigter Ketone und A1dehyd
Markus Peter Zink, Hans Richard Wolf, Ernst Peter Muller,Wolfhard Bernd Schweizer und Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     cubebol
    ÏàËÆ¶È:60%
Phytochemistry          1989          28          2202-2203
10-EPI-cubebolxyloside from Iphiona scabra
M. Abdel-Mogib,J. Jakupovic,A.M. Dawidar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     2'-(morpholin-4-ylcarbonyl)-5',6',7',8'-tetrahydro-4'H-spiro[cyclohexane-1,9'-[1,2,4]triazolo[5,1-b]quinazoline]
C14H22N4     ÏàËÆ¶È:60%
Journal of Heterocyclic Chemistry          2008          45          1419-1427
Synthesis,structure and some reactions of 4a',5',6',7',8',8a'-hexahydro-4'H-spiro[cyclohexane-1,9'-[1,2,4]triazolo[5,1-b]-quinazolines]
Victor M. Chernyshev,Dmitry A. Khoroshkin,Andrey N. Sokolov,Vitaly A. Taranushich,Eugene S. Gladkov,Svetlana V. Shishkina,Oleg V. Shishkin and Sergey M. Desenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     [(4aS,8aS)-3,4,4a,5,6,7,8,8a-Octahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]methanol
C15H26O     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Guaiacophine
C15H22O     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2010          7          2007-2015
Terpenes from the Soft Corals Litophyton arboreum and Sarcophyton ehrenbergi
Kamel H. Shaker, Michael M¨¹ller, M. Abdel Ghani, Hans-Martin Dahse and Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 21
    ÏàËÆ¶È:60%
Phytochemistry          1981          20          469-472
Sesquiterpenes from three Senecio species
Ferdinand Bohlmann, J¨¹rgen Ziesche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (-)-cubebol
    ÏàËÆ¶È:60%
Bioscience, Biotechnology, and Biochemistry          2008          72          611-614
Antifeedants against Locusta migratoria from the Japanese Cedar, Cryptomeria japonica II
Bin WU, Takehiro KASHIWAGI, Ikuhiro KURODA, Xiao Hui CHEN, Shin-ich TEBAYASHI and Chul-Sa KIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     laurobtusol
C15H26O     ÏàËÆ¶È:60%
Tetrahedron          1991          47          10101-10108
The structure of laurobtusol, a new rearranged sesquiterpenoid from the mediterranean red alga laurencia obtusa
Salvatore Caccamese, Vincenzo Amico, Placido Neri, Mario Foti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     alloisolongifolene
    ÏàËÆ¶È:60%
Tetrahedron          2003          59          409-418
Hydroxylation of sesquiterpenes by enzymes from chicory (Cichorium intybus L.) roots
Jan-Willem de Kraker, Marloes Schurink, Maurice C.R Franssen, Wilfried A König, Aede de Groot, Harro J Bouwmeester
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     11-bromo-8-drimene
    ÏàËÆ¶È:60%
Tetrahedron          1998          54          5635-5650
Synthesis of wiedendiol-A and wiedendiol-B from labdane diterpenes
Alejandro F. Barrero, Enrique J. Alvarez-Manzaneda, Rachid Chahboun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     pubescenone
C16H24O3     ÏàËÆ¶È:56.2%
Heterocycles          2007          71          1135-1139
Pubescenone, a New Marasmane Sesquiterpenoid from the Mushroom Lactarius pubescens
Hong-Jun Shao, Chun-Jiang Wang, Yun Dai, Fei Wang, Wan-Qiu Yang, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     compound 11
    ÏàËÆ¶È:56.2%
Phytochemistry          1985          24          2317-2323
Sesquiterpenes from pernettya furens
Shigeki Hosozawa, Iwao Miura, Masaru Kido, Orlando M¨´noz, Mariano Castillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     compound 20
C16H28O4     ÏàËÆ¶È:56.2%
Tetrahedron Letters          2005          46          1149-1153
Studies toward the total synthesis of di- and sesterterpenes with a dicyclopenta[a,d]cyclooctane skeleton. Construction of a versatile A/B ring building block via a ring-closing metathesis reaction and carbocationic rearrangement
Karol Michalak, Michał Michalak, Jerzy Wicha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     compound 17
    ÏàËÆ¶È:56.2%
Journal of the Chemical Society, Perkin Transactions 1          1995                   1513-1517
Synthesis and the absolute configuration of the sesquiterpene aldehyde tridensenal from the Taiwanese liverwort Bazzania tridens
Motoo Tori, Naomi Uchida, Aya Sumida, Hirosuke Furuta and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     (2R,5R,10S)-2-N-methyl axane
C16H31N     ÏàËÆ¶È:56.2%
Tetrahedron          2006          62          10393-10399
Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa
Christopher J. Wegerski, Rachel N. Sonnenschein, Freddy Cabriales, Frederick A. Valeriote, Teatulohi Matainaho, Phillip Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     (-)-(3aR,9aR,9bR)-3a,6,6,9a-tetramethyl-1,2,3a,4,6,7,8,9,9a,9b-decahydronaphtho[2,1-b]furan
C16H26O     ÏàËÆ¶È:56.2%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     compound 10
C16H28O3     ÏàËÆ¶È:56.2%
Tetrahedron          2001          57          8481-8493
Structure elucidation of arteannuin O, a novel cadinane diol from Artemisia annua, and the synthesis of arteannuins K, L, M and O
Lai-King Sy, Kung-Kai Cheung, Nian-Yong Zhu, Geoffrey D Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     4,8,18,22-Tetramethyl-1-oxa-9,10,16,17-tetraaza-cyclotetracosa-8,17-diene-2,11,15-trione
C23H40N4O4     ÏàËÆ¶È:56.2%
Russian Journal of Organic Chemistry          2011          47          1410-1415
Synthesis of macrolides containing an azine or hydrazide fragment via successive tishchenko disproportionation and [1 + 1]-condensation
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, R. R. Muslukhov and O. O. Shakhanova, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     5,18-dihydroxy-epi-homoverrucosane
    ÏàËÆ¶È:55.5%
Phytochemistry          1997          44          1495-1502
Epi-neoverrucosane- and epi-homoverrucosane-type diterpenoids from Fossombronia alaskana
Carola Grammes, Gunther Burkhardt, Michael Veith, Volker Huch, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     stemodin
    ÏàËÆ¶È:55%
Phytochemistry          2004          65          701-710
Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     stemodin
    ÏàËÆ¶È:55%
Phytochemistry          2004          65          2211-2217
Investigation of the importance of the C-2 and C-13 oxygen functions in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     stemodin
    ÏàËÆ¶È:55%
Phytochemistry          2002          59          57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     13,18-dihydroxystemodan-2-one
    ÏàËÆ¶È:55%
Phytochemistry          2002          59          57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     ent-1¦Á-hydroxykauran-12-one
C20H32O2     ÏàËÆ¶È:55%
Journal of Natural Products          1997          60          421-424
1-Hydroxyditerpenes from Two New Zealand Liverworts, Paraschistochila pinnatifolia and Trichocolea mollissima
Stephen D. Lorimer, Nigel B. Perry, Elaine J. Burgess, and Lysa M. Foster
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     compound 8
    ÏàËÆ¶È:55%
Chemistry of Natural Compounds          1981          17          408-410
A STUDY OF THE PROPERTIES AND 13C NMR SPECTRA OF PINIFOLIC ACID AND ITS DERIVATIVES
I. I. Bardyshev, A. S. Degtyarenko, T. I. Pekhk, and S. A. Makhnach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     3¦Á,18,19-trihydroxytrachylobane
C20H32O3     ÏàËÆ¶È:55%
Phytochemistry          2000          54          767-770
Diterpenoids from the roots of Croton macrostachys
Modest C.Kapingu, Dominique Guillaume, Zakaria H. Mbwambo, Mainen J. Moshi, Febronia C. Uliso, Rogasian L.A. Mahunnah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     18-hydroxystemodin
C20H34O4     ÏàËÆ¶È:55%
Journal of Natural Products          1991          Vol 54          1543
Preparation, Characterization, and Antiviral Activity of Microbial Metabolites of Stemodin
Charles D. Hufford, Farid A. Badria, Mohamed Abou-Karam, W. Thomas Shier, Robin D. Rogers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     Ar-abietatrien-12,16-oxide
C20H28O     ÏàËÆ¶È:55%
Phytochemistry          1982          21          643-646
Terpenoids from the seed of Thujopsis dolabrata var. Dolabrata
Shinichi Hasegawa, Yoshiyuki Hirose
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     Totara-8,11,13-triene 7¦Á,13-diol
    ÏàËÆ¶È:55%
Bioorganic & Medicinal Chemistry          2000          8          1663-1675
The synthesis and antibacterial activity of totarol derivatives. part 3: modification of ring-B
Gary B Evans, Richard H Furneaux, Graeme J Gainsford, Michael P Murphy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     3¦Á-Hydroxy-T-muurolol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          99-101
T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes
Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     sarmentol G
C13H24O2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2007          55(3)          435-441
Bioactive Constituents from Chinese Natural Medicines. XXII.1) Absolute Structures of New Megastigmane Glycosides, Sedumosides E1,E2, E3, F1, F2, and G, from Sedum sarmentosum (Crassulaceae)
Toshio MORIKAWA,Yi ZHANG,Seikou NAKAMURA,Hisashi MATSUDA,Osamu MURAOKA,and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     1¦Â,11-dihydroxy-5-eudesmene
    ÏàËÆ¶È:53.3%
Phytochemistry          2004          65          127-137
ent-Clerodane diterpenes and other constituents from the liverwort Adelanthus lindenbergianus (Lehm.) Mitt.
Barbara Blä s, Josef Zapp, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     (+)-9-hydroxyselina-4,11-diene
C15H24O     ÏàËÆ¶È:53.3%
Phytochemistry          2002          61          79-91
Volatile components from European liverworts Marsupella emarginata, M. aquatica and M. alpina
Adewale Martins Adio, Claudia Paua, Wilfried A. König, Hermann Muhle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     kanshone G
C15H24O2     ÏàËÆ¶È:53.3%
Phytochemistry          2002          59          845-849
Guaiane- and aristolane-type sesquiterpenoids of Nardostachys chinensis roots
Masa-aki Tanitsu, Yoshiaki Takaya, Megumi Akasaka, Masatake Niwa,Yoshiteru Oshima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     1¦Á,4¦Â,8¦Á-trihydroxyeudesman-6-one
C15H26O4     ÏàËÆ¶È:53.3%
Phytochemistry          2001          58          891-895
Biotransformation of 4b-hydroxyeudesmane-1,6-dione by Gliocladium roseum and Exserohilum halodes
Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Francisco Rivas, Jos¨¦ M. Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     3,4-epoxypalisadin B
C15H24Br2O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          1314-1317
Terpenoids from Laurencia luzonensis
Masayuki Kuniyoshi, Paul G. Wahome, Takayuki Miono, Takeshi Hashimoto, Muneaki Yokoyama, Keshab L. Shrestha, and Tatsuo Higa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     isolemnalol
C15H24O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          1650-1653
Steroids and Sesquiterpenoids from the Soft Corals Dendronephthya gigantea and Lemnalia cervicorni
Chang-Yih Duh, Ali A. H. El-Gamal, Pei-Ying Song, Shang-Kwei Wang, and Chang-Feng Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-08-23 22:04:04
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