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1 .     1R,2R,4R-ÈýôÇ»ù±¡ºÉÍé
C10H20O3     ÏàËÆ¶È:70%
Chinese Pharmaceutical Journal          2003          38          333-335
Study on chemical components of Epimedium leptorrhizum
HAN Bing, SHEN Tong, JU Jian hua, YANG Jun shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (+) (1R*, 2R*, 4R*)-trihydroxy-p-menth-3-ene
C10H20O3     ÏàËÆ¶È:60%
Phytochemistry          2006          67          2103-2109
¦Á-Pinene-type monoterpenes and other constituents from Artemisia suksdorfii
Ahmed A. Mahmoud , Ahmed A. Ahmed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (4S)-3¦Á,10¦Á,12,15-tetrahydroxycadinane
    ÏàËÆ¶È:60%
Phytochemistry          2002          59          479-488
Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740
Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     4¦Á,7¦Â-Dihydroxyeudesmane
C15H28O2     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2006          8          723-731
Eudesmane-type sesquiterpenoids from the liverwort Lepidozia fauriana
H.-S. SHY and C.-L. WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Plenoxide
C15H26O2     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2005          7          847-852
Chemical constituents from Schisandra plena
R.-T. LI, A.-H. ZHAO, Y.-H. SHENG, Z. NA and H.-D. SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     7-(methylsulfamyl)heptanenitrile
C8H15NS     ÏàËÆ¶È:60%
Phytochemistry          1998          49          1959-1965
Macrocyclic bisbibenzyls in cultured cells of the liverwort, Heteroscyphus planus
Kensuke Nabet¦Á, Shinichi Ohkubo, Reiko Hozumi, Kenji Katoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     rel-(1S,2R,4R,8S)-p-menthane-1,2,8,9-tetrol
C10H20O4     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2002          50          66-72
Water-Soluble Constituents of Caraway: Carvone Derivatives and Their Glucosides
Tetsuko Matsumura, Toru Ishikawa and Junichi Kitajima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     4¦Â-hydroxy-1-menthol
    ÏàËÆ¶È:60%
Phytochemistry          1988          27          3861-3869
Preparation of biologically active substances and animal and microbial metabolites from menthols,cineoles and kauranes
Yoshinori Asakawa,Reiko Matsuda,Motoo Tori,Toshihiro Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     2-exo-hydroxy-1,8-cineole
    ÏàËÆ¶È:60%
Phytochemistry          1988          27          3861-3869
Preparation of biologically active substances and animal and microbial metabolites from menthols,cineoles and kauranes
Yoshinori Asakawa,Reiko Matsuda,Motoo Tori,Toshihiro Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Compound h3
    ÏàËÆ¶È:60%
Magnetic Resonance in Chemistry          2008          46          1168-1174
Structural elucidation of propargylated products of 3-substituted-1, 2, 4-triazole-5-thiols by NMR techniques (pages 1168¨C1174)
Preeti M. Chaudhary, Sayalee R. Chavan, M. Kavitha, Shailaja P. Maybhate, Sunita R. Deshpande, Anjali P. Likhite and P. R. Rajamohanan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (1R,3R)-(3)-1-(2-bromoethyl)-2,2-dimethyl-3-(2-oxopropyl)cyclopropane
    ÏàËÆ¶È:60%
Russian Journal of Organic Chemistry          2003          39          75-81
Approaches to Epothilone Carboanalogs Starting from ¦¤3-Carene
F. A. Akbutina, I. F. Sadretdinov, O. M. Kuznetsov, E. V. Vasil'eva and M. S. Miftakhov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     1S,2R,4S-trihydroxyl-p-methane
    ÏàËÆ¶È:60%
Food Chemistry          2010          118          228-238
Unusual sesquiterpene lactones with a new carbon skeleton and new acetylenes from Ajania przewalskii
Ying Zhu, Li-Xia Zhang, Yan Zhao, Guo-Du Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (S)-(+)-diisopropyl (4-bromo-1-mesyloxybutyl)phosphonate
C11H24BrO6PS     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2011                   1870-1879
Chemoenzymatic Synthesis of Phosphonic Acid Analogues of L-Lysine, L-Proline, L-Ornithine, and L-Pipecolic Acid of 99 % ee ¨C Assignment of Absolute Configuration to (¨C)-Proline
Frank Wuggenig, Anna Schweifer, Kurt Mereiter and Friedrich Hammerschmidt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (3S,4S,6R)-2,7-dimethyl-3,4,6-octanetriol
C10H22O3     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2010                   3146-3151
Highly Stereoselective Synthesis of syn-1,3-Diols through a Sequential Titanium-Mediated Aldol Reaction and LiBH4 Reduction
Judit Esteve, S¨°nia Matas, Miquel Pellicena, Javier Velasco, Pedro Romea, F¨¨lix Urp¨ª and Merc¨¨ Font-Bardia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     5-(adamant-1-ylmethoxy)pent-2-ene
C16H26O     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2010                   1258-1283
Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism
Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 9b
    ÏàËÆ¶È:60%
Australian Journal of Chemistry          1994          47          1509-1521
2,9-Dihydroxy- and 2,10-Dihydroxy-1,8-cineole. Two New Possum Urinary Metabolites
RM Carman, AC Garner and KD Klika
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (1R,4R,5R,8R)-4,8-dimethyl-2-oxabicyclo[3.3.1]nonan-8-ol
C10H18O2     ÏàËÆ¶È:60%
Australian Journal of Chemistry          1995          48          1301-1309
The Synthesis of Two C4 Epimers of 4,8-Dimethyl-2-oxabicyclo[3.3.1]nonan-8-ol (1-Hydroxy-2,9-cineole)
RM Carman and AC Garner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (1R,2R,4R)-1-methyl-4-(1-methylethyl)-1,2,4-cyclohexanetriol
C10H20O3     ÏàËÆ¶È:60%
Bioscience, Biotechnology, and Biochemistry          2012          76          1904-1908
Cleavage of ¦Á-Dicarbonyl Compounds by Terpene Hydroperoxide
Ryu-ichiro NAGAMATSU, Shinya MITSUHASHI, Kengo SHIGETOMI, Makoto UBUKATA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (+)-2-endo-hydroxy-1,8-cineole
    ÏàËÆ¶È:60%
Journal of Agricultural and Food Chemistry          1989          37          222-226
Hydroxycineole: four new metabolites of 1,8-cineole in rabbits
Mitsuo Miyazawa, Hiromu Kameoka, Kunio Morinaga, Kenji Negoro, Nobuo Mura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     1¦Â,4¦Â,7¦Á-trihydroxyeudesmane
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2012          37          3430-3433
Chemical constituents of Acorus calamus
QIAO Di; GAN Li-she; MO Jian-xia; ZHOU Chang-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     4-pentylcyclohex-3-ene-1¦Á,2¦Â-diol
C11H20O2     ÏàËÆ¶È:54.5%
Journal of Asian Natural Products Research          2009          11          805-810
Two new compounds from the roots of Ligusticum chuanxiong
Xin-Liang Changa, Zhi-Yong Jianga, Yun-Bao Maa, Xue-Mei Zhanga,Karl W.K. Tsimb and Ji-Jun Chena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     n-Tritetracontan-5¦Á-ol
C43H88O     ÏàËÆ¶È:54.5%
Chinese Journal of Chemistry          2007          25          843-848
New Aliphatic Alcohol and Ester Constituents from Rice Hulls of Oryza sativa
ILL-Min Chung, Mohd Ali, Se-Chul Chun, Cheng-Wu Jin, Dong-Ha Cho, Seung-Beom Hong and Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     (1¦Á,4a¦Â,8a¦Á)-4a-methyldecahydronaphthalene-1,8a-diol
C11H20O2     ÏàËÆ¶È:54.5%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (1R,4R,5R,8S,9S,13S)-caryolane-5,8,13-triol
C15H26O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2006          69(10)          1429-1434
Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (−-Caryophyllene Oxide and Its Derivatives
Muhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     1¦Â,4¦Â,7¦Á-trihydroxyeudesmane
C15H28O3     ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2003          28          342-344
Studies on the Constituents in Rhizome of Homalomena occuta
HU Yongmei, YANG Zhonglin, YE Wencai, CHONG Qihou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     (E)-7¦ÁH-germacra-4,10(14)-diene-1b,6¦Á,11-triol
    ÏàËÆ¶È:53.3%
Phytochemistry          1999          51          529-541
Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring
Alejandro F. Barrero, M. Mar Herrador, Jose F.Quilez, Ramon Alvarez-Manzaneda, Dolores Portal, Jose A. Gavin, Dolores G. Gravalos, M.S.J. Simmonds, W.M. Blaney
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     Prostantherol
    ÏàËÆ¶È:53.3%
Phytochemistry          1994          36          957-960
Antimicrobial sesquiterpenes from Prostanthera aff. melissifolia and P. rotundifolia
Joanne E. Dillar, Michael D. Cole, Alexander I. Gray, Simon Gibbons, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     compound 1
C15H26O     ÏàËÆ¶È:53.3%
Phytochemistry          1992          31          2153-2154
A sesquiterpene alcohol from Litsea amara
S.A. Achmad, E.L. Ghisalberti, E.H. Hakim, L. Makmur, M. Manurung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     1¦Â,4¦Â,7¦Â-eudesmanetriol
    ÏàËÆ¶È:53.3%
Natural Product Research          2012          26          850-858
A new sesquiterpenoid from the rhizomes of Homalomena sagittifolia
K.C. Wong, Abdul Hamid, I.M.S. Eldeen, M. Zaini Asmawi,S. Baharuddin, H.S. Abdillahi and J. Van Staden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     compound 14
    ÏàËÆ¶È:53.3%
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

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31 .     (+)-10¦Â,14-dihydroxy-allo-aromadendrane
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          2003          41          1034-1037
Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane
Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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