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    1 .     N-methyl-2-(2-hydroxybutyl)-6-(2-hydroxypentylpiperidine)
        ÏàËÆ¶È:61.5%
    Zeitschrift f¨¹r Naturforschung C          2002          57          81-84
    Antinociceptive Activity of the Natural Piperidine Alkaloid Hydrochlorides from Syphocampylus verticellatus
    O. G. Miguel, A. R. S. Santos, J. B. Calixto, F. D. Monache, and R. A. Yunes
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    2 .     1¦Á-hydroxy-3-deoxypseudoanisatin
    C15H22O6     ÏàËÆ¶È:60%
    Chemical & Pharmaceutical Bulletin          1999          47          1749-1752
    Structures of Novel Sesquiterpenes from the Pericarps of Illicium merrillianum
    Jian-mei HUANG,Chun-shu YANG,Hai WANG,Qiu-ming WU,Jia-ling WANG and Yoshiyasu FUKUYAMA
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    3 .     nootkatone-1,10-11,12-diepoxide
    C15H22O3     ÏàËÆ¶È:60%
    molecules          2011          16          4775-4785
    Biologically Important Eremophilane Sesquiterpenes from Alaska Cedar Heartwood Essential Oil and Their Semi-Synthetic Derivatives
    Mohammad A. Khasawneh, Yeping Xiong, Javier Peralta-Cruz and Joe J. Karchesy
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    4 .     (7E)-7-Ethyl-10-hydroxyundec-7-ene-3,6-dione
    C13H22O3     ÏàËÆ¶È:53.8%
    Helvetica Chimica Acta          2008          Vol. 91          741
    Novel Polyketides Isolated from Streptomyces sp.
    Jian Li, Chun-Hua Lu, and Yue-Mao Shen
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    5 .     ascleposide B(4a)
    C13H20O5     ÏàËÆ¶È:53.8%
    Chemical & Pharmaceutical Bulletin          2000          48(12)          1908-1911
    5, 11-Epoxymegastigmanes from the Leaves of Asclepias fruticosa
    Fumiko ABE and Tatsuo YAMAUCHI
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    6 .     kinganone
    C13H19NO2     ÏàËÆ¶È:53.8%
    Planta Medica          2003          69          1066-1068
    A New Indolizinone from Polygonatum kingianum
    Yi-Fen Wang,Chun-Hua Lu,Guo-Fang Lai,Jian-Xin Cao,Shi-De Luo
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    7 .     cucubalactone
    C13H20O5     ÏàËÆ¶È:53.8%
    Planta Medica          2002          68          91-94
    New Norsesquiterpenoids from Cucubalus baccifer
    Yong-Xian Cheng,Jun Zhou,Shi-Ming Deng,Ning-Hua Tan
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    8 .     (3S,4R,5S,7S,8S,9S)-3,8-epoxy-7-hydroxy-4,8-dimethylperhydrocyclopenta[c]pyran
        ÏàËÆ¶È:53.8%
    Journal of Natural Products          2010          73          632-638
    Iridoids and Lignans from Valeriana jatamansi
    Sheng Lin, Tao Chen, Xiao-Hua Liu, Yun-Heng Shen, Hui-Liang Li, Lei Shan, Run-Hui Liu, Xi-Ke Xu, Wei-Dong Zhang and Hui Wang
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    9 .     compound 30
    C10H20O2     ÏàËÆ¶È:53.8%
    Phytochemistry          1991          30          3981-3987
    Biotransformation of monoterpenoids, (−- and menthols, terpinolene and carvotanacetone by Aspergillus species
    Yoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    10 .     cucubalactone
    C13H20O5     ÏàËÆ¶È:53.8%
    Chinese Traditional and Herbal Drugs          2009          40          681-683
    Chemical constituents in butanol extraction from stems and leaves of Arachis hypogaea
    HE Jing-jing; XIE Jing; HAN Zhu-zhen; SHAO Yi-ci; QIAN Fu-gang
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    11 .     3-¶¡Ñõ¼×»ù-5,6,7,8-ËÄÇâ-8-ßÅßáÁ¨àºÍª
    C13H19NO2     ÏàËÆ¶È:53.8%
    Chinese Traditional and Herbal Drugs          2008          39          825-828
    µá»Æ¾«µÄ»¯Ñ§³É·ÖÑо¿(¢ò)
    ÀîÏþ;À´¹ú·À;ÍõÒ×·Ò;Õű£¹ú;ÂÞÊ¿µÂ
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    12 .     compound 22
    C12H20O     ÏàËÆ¶È:53.8%
    Tetrahedron Letters          2004          45          6591-6594
    Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones
    Ronald V. Lerum, John D. Chisholm
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    13 .     compound 24
    C13H20O4     ÏàËÆ¶È:53.8%
    Tetrahedron          2012          68          1171-1176
    Construction of functionalized B/C/D ring system of C19-diterpenoid alkaloids via intramolecular Diels¨CAlder reaction followed by Wagner¨CMeerwein rearrangement
    Hang Cheng, Liang Xu, De-Lin Chen, Qiao-Hong Chen, Feng-Peng Wang
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    14 .     compound 5
    C12H24O3S     ÏàËÆ¶È:53.8%
    Tetrahedron          2002          58          6405-6412
    Hedathiosulfonic acids A and B, novel thiosulfonic acids from the deep-sea urchin Echinocardium cordatum
    Masaki Kita, Masami Watanabe, Noboru Takada, Kiyotake Suenaga, Kaoru Yamada, Daisuke Uemura
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    15 .     squalestatin U2
        ÏàËÆ¶È:53.8%
    The Journal of Antibiotics          1994          47          740-754
    THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF Phoma V. MINOR METABOLITES
    WILLIAM M. BLOWS, GRAHAM FOSTER, STEPHEN J. LANE, DAVID NOBLE, JOHN E. PIERCEY, PHILIP J. SIDEBOTTOM, GRAHAM WEBB
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    16 .     compound 7
        ÏàËÆ¶È:53.8%
    Journal of the American Chemical Society          2004          126          187-193
    Schulzeines A−C, New ¦Á-Glucosidase Inhibitors from the Marine Sponge Penares schulzei1
    Kentaro Takada, Taisuke Uehara, Yoichi Nakao, Shigeki Matsunaga, Rob W. M. van Soest, and Nobuhiro Fusetani
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    17 .     3S-Methyl 2-Butoxycarbonylamino-3-[(3-hydroxy-1-propylpropyl)sulfanyl]propanoate
        ÏàËÆ¶È:53.8%
    Journal of Agricultural and Food Chemistry          2008          56          3758-3763
    Synthesis of the Individual Diastereomers of the Cysteine Conjugate of 3-Mercaptohexanol (3-MH)
    Kevin H. Pardon, Sean D. Graney, Dimitra L. Capone, Jan H. Swiegers, Mark A. Sefton and Gordon M. Elsey
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    18 .     (4S)-3¦Á,14-dihydroxycadin-10(15)-ene
    C15H26O2     ÏàËÆ¶È:53.3%
    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

    19 .     compound 4
    C15H20BrClO     ÏàËÆ¶È:53.3%
    Chemical Communications          1985                   260-261
    Rhodolaureol and Rhodolauradiol, Two New Halogenated Tricyclic Sesquiterpenes from a Marine Alga
    Antonio G. Gonzalez, Julio D. Martin, * Victor S. Martin, Ricardo Perez, Bruce Tagle, and Jon Clardy
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    20 .     8-epiisolipidiol
        ÏàËÆ¶È:53.3%
    Planta Medica          2011          77          380-382
    New Guaiane Sesquiterpene Lactones from Ixeris dentata
    Mi-Ran Cha, Yeon Hee Choi, Chun Whan Choi, Dae Seok Yoo, Young Sup Kim, Sang Un Choi, Young Ho Kim, Shi Yong Ryu
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    21 .     compound 17
        ÏàËÆ¶È:53.3%
    Australian Journal of Chemistry          1989          42          1591-1603
    Tropical Marine Algae. III. New Sesquiterpenes From Laurencia majuscula (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae)
    JC Coll and AD Wright
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    22 .     Decurrenside E
    C19H24O8     ÏàËÆ¶È:52.9%
    Journal of Natural Products          2012          75          88-92
    Benzyl Benzoate Glycoside and 3-Deoxy-d-manno-2-octulosonic Acid Derivatives from Solidago decurrens
    Ken Shiraiwa, Shen Yuan, Ayako Fujiyama, Yosuke Matsuo, Takashi Tanaka, Zhi-Hong Jiang, and Isao Kouno
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    23 .     9-bromo-7-methyltricyclo[5.4.0.02,9]undecan-8-one-3-spiro-1'-cyclopropane
    C14H19OBr     ÏàËÆ¶È:50%
    Journal of Natural Products          2003          66          520-523
    An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene
    Sasan Karimi, and Paula Tavares
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    24 .     9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one
    C14H21OBr     ÏàËÆ¶È:50%
    Journal of Natural Products          2003          66          520-523
    An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene
    Sasan Karimi, and Paula Tavares
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    25 .     montiporic acid A
    C14H20O3     ÏàËÆ¶È:50%
    Journal of Natural Products          1996          59          796-797
    Montiporic Acids A and B, Cytotoxic and Antimicrobial Polyacetylene Carboxylic Acids from Eggs of the Scleractinian Coral Montipora digitata
    Nobuhiro Fusetani, Takeo Toyoda, Naoki Asai, Shigeki Matsunaga, and Tadashi Maruyama
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    26 .     incarviditone
    C16H20O6     ÏàËÆ¶È:50%
    Chemistry & Biodiversity          2009          6          779-783
    Incarviditone: A Novel Cytotoxic Benzofuranone Dimer from Incarvillea delavayi Bureau et Franchet
    Yu-Qi Chen, Yun-Heng Shen, Yong-Qing Su, Ling-Yi Kong, and Wei-Dong Zhang
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    27 .     incarvmarein B
    C16H24O6     ÏàËÆ¶È:50%
    Journal of Asian Natural Products Research          2009          11          523-528
    Cyclohexyl-ethanol derivatives from the roots of Incarvillea mairei
    Zheng-Sheng Huangac, Yue-Hu Peic, Yun-Heng Shena, Sheng Lina, Chun-Mei Liua,Min Lud and Wei-Dong Zhangab
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    28 .     oblongolide W1
    C16H24O4     ÏàËÆ¶È:50%
    Journal of Natural Products          2010          73          55-59
    Oblongolides from the Endophytic Fungus Phomopsis sp. BCC 9789
    Taridaporn Bunyapaiboonsri, Seangaroon Yoiprommarat, Prasert Srikitikulchai, Kitlada Srichomthong and Saisamorn Lumyong
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    29 .     rengyoside A
        ÏàËÆ¶È:50%
    Phytochemistry          1995          39          235-241
    Cyclohexylethanoids and related glucosides from Millingtonia hortensis
    Takeshi Hase, Yuka Kawamoto, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Chayan Picheansoonthon
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    30 .     compound 15
        ÏàËÆ¶È:50%
    Phytochemistry          1994          35          713-719
    Compounds with the labdane skeleton from Halimium viscosum
    Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    31 .     N-(((1R,2S,4S,5R)-2-(tert-butyldimethylsilyloxy)-5-(hydroxymethyl)-4-methylcyclohexyl)methyl)acetamide
    C16H33NO4Si     ÏàËÆ¶È:50%
    Organic Letters          2009          Vol.11,No.1          217-220
    Total Synthesis and Structural Confirmation of Brevisamide, a New Marine Cyclic Ether Alkaloid from the Dinoflagellate Karenia brevis
    Takefumi Kuranaga, Tomohiro Shirai, Daniel G. Baden, Jeffrey L. C. Wright,Masayuki Satake, and Kazuo Tachibana
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    32 .     compound 15
    C16H31NO4     ÏàËÆ¶È:50%
    Heterocycles          2010          80          395-408
    Synthesis of (+)-Batzelladine K
    Miyuki Sekine, Yumi Iijima, Osamu Iwamoto, and Kazuo Nagasawa
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    33 .     (5R,8S,8as)-N-methoxy-N-methyl-5-propyloctahydroindolizine-8-carboxamide
        ÏàËÆ¶È:50%
    Heterocycles          2009          79          935-953
    Formal Synthesis of (5R,8R,8aS)-Indolizidine 209I via Enaminones Incorporating Weinreb Amides
    Charles B. de Koning, Joseph P. Michael, and Darren L. Riley
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    34 .     tert-Butyl 7-methyl-3-oxoundecanoate
        ÏàËÆ¶È:50%
    Bioscience, Biotechnology, and Biochemistry          2010          74          119-124
    Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth
    Tomonori TAGURI, Rei YAMAKAWA, Yasushi ADACHI, Kenji MORI and Tetsu ANDO
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    35 .     Talaperoxide C
    C14H20O4     ÏàËÆ¶È:50%
    Journal of Natural Products          2011          74          1230-1235
    Cytotoxic Norsesquiterpene Peroxides from the Endophytic Fungus Talaromyces flavus Isolated from the Mangrove Plant Sonneratia apetala
    Hanxiang Li, Hongbo Huang, Changlun Shao, Huarong Huang, Jieyi Jiang, Xun Zhu, Yayue Liu, Lan Liu, Yongjun Lu, Mengfeng Li, Yongcheng Lin, and Zhigang She
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-12-11 18:37:16
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ralonxu: ½ð±Ò+3, ¡ï¡ï¡ïºÜÓаïÖú, лл£¬²»ºÃÒâ˼£¬Ö»ÄܸøÄã3¸ö½ð±ÒÁË£¬ÒòΪÓÐÈËÒѾ­»Ø¹ýÁË 2012-12-11 22:03:12
1 .     N-methyl-2-(2-hydroxybutyl)-6-(2-hydroxypentylpiperidine)
    ÏàËÆ¶È:61.5%
Zeitschrift f¨¹r Naturforschung C          2002          57          81-84
Antinociceptive Activity of the Natural Piperidine Alkaloid Hydrochlorides from Syphocampylus verticellatus
O. G. Miguel, A. R. S. Santos, J. B. Calixto, F. D. Monache, and R. A. Yunes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     1¦Á-hydroxy-3-deoxypseudoanisatin
C15H22O6     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1999          47          1749-1752
Structures of Novel Sesquiterpenes from the Pericarps of Illicium merrillianum
Jian-mei HUANG,Chun-shu YANG,Hai WANG,Qiu-ming WU,Jia-ling WANG and Yoshiyasu FUKUYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     nootkatone-1,10-11,12-diepoxide
C15H22O3     ÏàËÆ¶È:60%
molecules          2011          16          4775-4785
Biologically Important Eremophilane Sesquiterpenes from Alaska Cedar Heartwood Essential Oil and Their Semi-Synthetic Derivatives
Mohammad A. Khasawneh, Yeping Xiong, Javier Peralta-Cruz and Joe J. Karchesy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     (7E)-7-Ethyl-10-hydroxyundec-7-ene-3,6-dione
C13H22O3     ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          2008          Vol. 91          741
Novel Polyketides Isolated from Streptomyces sp.
Jian Li, Chun-Hua Lu, and Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     ascleposide B(4a)
C13H20O5     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          2000          48(12)          1908-1911
5, 11-Epoxymegastigmanes from the Leaves of Asclepias fruticosa
Fumiko ABE and Tatsuo YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     kinganone
C13H19NO2     ÏàËÆ¶È:53.8%
Planta Medica          2003          69          1066-1068
A New Indolizinone from Polygonatum kingianum
Yi-Fen Wang,Chun-Hua Lu,Guo-Fang Lai,Jian-Xin Cao,Shi-De Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     cucubalactone
C13H20O5     ÏàËÆ¶È:53.8%
Planta Medica          2002          68          91-94
New Norsesquiterpenoids from Cucubalus baccifer
Yong-Xian Cheng,Jun Zhou,Shi-Ming Deng,Ning-Hua Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     (3S,4R,5S,7S,8S,9S)-3,8-epoxy-7-hydroxy-4,8-dimethylperhydrocyclopenta[c]pyran
    ÏàËÆ¶È:53.8%
Journal of Natural Products          2010          73          632-638
Iridoids and Lignans from Valeriana jatamansi
Sheng Lin, Tao Chen, Xiao-Hua Liu, Yun-Heng Shen, Hui-Liang Li, Lei Shan, Run-Hui Liu, Xi-Ke Xu, Wei-Dong Zhang and Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     compound 30
C10H20O2     ÏàËÆ¶È:53.8%
Phytochemistry          1991          30          3981-3987
Biotransformation of monoterpenoids, (−- and menthols, terpinolene and carvotanacetone by Aspergillus species
Yoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     cucubalactone
C13H20O5     ÏàËÆ¶È:53.8%
Chinese Traditional and Herbal Drugs          2009          40          681-683
Chemical constituents in butanol extraction from stems and leaves of Arachis hypogaea
HE Jing-jing; XIE Jing; HAN Zhu-zhen; SHAO Yi-ci; QIAN Fu-gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     3-¶¡Ñõ¼×»ù-5,6,7,8-ËÄÇâ-8-ßÅßáÁ¨àºÍª
C13H19NO2     ÏàËÆ¶È:53.8%
Chinese Traditional and Herbal Drugs          2008          39          825-828
µá»Æ¾«µÄ»¯Ñ§³É·ÖÑо¿(¢ò)
ÀîÏþ;À´¹ú·À;ÍõÒ×·Ò;Õű£¹ú;ÂÞÊ¿µÂ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     compound 22
C12H20O     ÏàËÆ¶È:53.8%
Tetrahedron Letters          2004          45          6591-6594
Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones
Ronald V. Lerum, John D. Chisholm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     compound 24
C13H20O4     ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          1171-1176
Construction of functionalized B/C/D ring system of C19-diterpenoid alkaloids via intramolecular Diels¨CAlder reaction followed by Wagner¨CMeerwein rearrangement
Hang Cheng, Liang Xu, De-Lin Chen, Qiao-Hong Chen, Feng-Peng Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     compound 5
C12H24O3S     ÏàËÆ¶È:53.8%
Tetrahedron          2002          58          6405-6412
Hedathiosulfonic acids A and B, novel thiosulfonic acids from the deep-sea urchin Echinocardium cordatum
Masaki Kita, Masami Watanabe, Noboru Takada, Kiyotake Suenaga, Kaoru Yamada, Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     squalestatin U2
    ÏàËÆ¶È:53.8%
The Journal of Antibiotics          1994          47          740-754
THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF Phoma V. MINOR METABOLITES
WILLIAM M. BLOWS, GRAHAM FOSTER, STEPHEN J. LANE, DAVID NOBLE, JOHN E. PIERCEY, PHILIP J. SIDEBOTTOM, GRAHAM WEBB
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     compound 7
    ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          2004          126          187-193
Schulzeines A−C, New ¦Á-Glucosidase Inhibitors from the Marine Sponge Penares schulzei1
Kentaro Takada, Taisuke Uehara, Yoichi Nakao, Shigeki Matsunaga, Rob W. M. van Soest, and Nobuhiro Fusetani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     3S-Methyl 2-Butoxycarbonylamino-3-[(3-hydroxy-1-propylpropyl)sulfanyl]propanoate
    ÏàËÆ¶È:53.8%
Journal of Agricultural and Food Chemistry          2008          56          3758-3763
Synthesis of the Individual Diastereomers of the Cysteine Conjugate of 3-Mercaptohexanol (3-MH)
Kevin H. Pardon, Sean D. Graney, Dimitra L. Capone, Jan H. Swiegers, Mark A. Sefton and Gordon M. Elsey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     (4S)-3¦Á,14-dihydroxycadin-10(15)-ene
C15H26O2     ÏàËÆ¶È:53.3%
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
--------------------------------------------------------------------------------

19 .     compound 4
C15H20BrClO     ÏàËÆ¶È:53.3%
Chemical Communications          1985                   260-261
Rhodolaureol and Rhodolauradiol, Two New Halogenated Tricyclic Sesquiterpenes from a Marine Alga
Antonio G. Gonzalez, Julio D. Martin, * Victor S. Martin, Ricardo Perez, Bruce Tagle, and Jon Clardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     8-epiisolipidiol
    ÏàËÆ¶È:53.3%
Planta Medica          2011          77          380-382
New Guaiane Sesquiterpene Lactones from Ixeris dentata
Mi-Ran Cha, Yeon Hee Choi, Chun Whan Choi, Dae Seok Yoo, Young Sup Kim, Sang Un Choi, Young Ho Kim, Shi Yong Ryu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     compound 17
    ÏàËÆ¶È:53.3%
Australian Journal of Chemistry          1989          42          1591-1603
Tropical Marine Algae. III. New Sesquiterpenes From Laurencia majuscula (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae)
JC Coll and AD Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     Decurrenside E
C19H24O8     ÏàËÆ¶È:52.9%
Journal of Natural Products          2012          75          88-92
Benzyl Benzoate Glycoside and 3-Deoxy-d-manno-2-octulosonic Acid Derivatives from Solidago decurrens
Ken Shiraiwa, Shen Yuan, Ayako Fujiyama, Yosuke Matsuo, Takashi Tanaka, Zhi-Hong Jiang, and Isao Kouno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     9-bromo-7-methyltricyclo[5.4.0.02,9]undecan-8-one-3-spiro-1'-cyclopropane
C14H19OBr     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          520-523
An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene
Sasan Karimi, and Paula Tavares
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one
C14H21OBr     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          520-523
An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene
Sasan Karimi, and Paula Tavares
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     montiporic acid A
C14H20O3     ÏàËÆ¶È:50%
Journal of Natural Products          1996          59          796-797
Montiporic Acids A and B, Cytotoxic and Antimicrobial Polyacetylene Carboxylic Acids from Eggs of the Scleractinian Coral Montipora digitata
Nobuhiro Fusetani, Takeo Toyoda, Naoki Asai, Shigeki Matsunaga, and Tadashi Maruyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     incarviditone
C16H20O6     ÏàËÆ¶È:50%
Chemistry & Biodiversity          2009          6          779-783
Incarviditone: A Novel Cytotoxic Benzofuranone Dimer from Incarvillea delavayi Bureau et Franchet
Yu-Qi Chen, Yun-Heng Shen, Yong-Qing Su, Ling-Yi Kong, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     incarvmarein B
C16H24O6     ÏàËÆ¶È:50%
Journal of Asian Natural Products Research          2009          11          523-528
Cyclohexyl-ethanol derivatives from the roots of Incarvillea mairei
Zheng-Sheng Huangac, Yue-Hu Peic, Yun-Heng Shena, Sheng Lina, Chun-Mei Liua,Min Lud and Wei-Dong Zhangab
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     oblongolide W1
C16H24O4     ÏàËÆ¶È:50%
Journal of Natural Products          2010          73          55-59
Oblongolides from the Endophytic Fungus Phomopsis sp. BCC 9789
Taridaporn Bunyapaiboonsri, Seangaroon Yoiprommarat, Prasert Srikitikulchai, Kitlada Srichomthong and Saisamorn Lumyong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     rengyoside A
    ÏàËÆ¶È:50%
Phytochemistry          1995          39          235-241
Cyclohexylethanoids and related glucosides from Millingtonia hortensis
Takeshi Hase, Yuka Kawamoto, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Chayan Picheansoonthon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     compound 15
    ÏàËÆ¶È:50%
Phytochemistry          1994          35          713-719
Compounds with the labdane skeleton from Halimium viscosum
Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     N-(((1R,2S,4S,5R)-2-(tert-butyldimethylsilyloxy)-5-(hydroxymethyl)-4-methylcyclohexyl)methyl)acetamide
C16H33NO4Si     ÏàËÆ¶È:50%
Organic Letters          2009          Vol.11,No.1          217-220
Total Synthesis and Structural Confirmation of Brevisamide, a New Marine Cyclic Ether Alkaloid from the Dinoflagellate Karenia brevis
Takefumi Kuranaga, Tomohiro Shirai, Daniel G. Baden, Jeffrey L. C. Wright,Masayuki Satake, and Kazuo Tachibana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     compound 15
C16H31NO4     ÏàËÆ¶È:50%
Heterocycles          2010          80          395-408
Synthesis of (+)-Batzelladine K
Miyuki Sekine, Yumi Iijima, Osamu Iwamoto, and Kazuo Nagasawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     (5R,8S,8as)-N-methoxy-N-methyl-5-propyloctahydroindolizine-8-carboxamide
    ÏàËÆ¶È:50%
Heterocycles          2009          79          935-953
Formal Synthesis of (5R,8R,8aS)-Indolizidine 209I via Enaminones Incorporating Weinreb Amides
Charles B. de Koning, Joseph P. Michael, and Darren L. Riley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     tert-Butyl 7-methyl-3-oxoundecanoate
    ÏàËÆ¶È:50%
Bioscience, Biotechnology, and Biochemistry          2010          74          119-124
Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth
Tomonori TAGURI, Rei YAMAKAWA, Yasushi ADACHI, Kenji MORI and Tetsu ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     Talaperoxide C
C14H20O4     ÏàËÆ¶È:50%
Journal of Natural Products          2011          74          1230-1235
Cytotoxic Norsesquiterpene Peroxides from the Endophytic Fungus Talaromyces flavus Isolated from the Mangrove Plant Sonneratia apetala
Hanxiang Li, Hongbo Huang, Changlun Shao, Huarong Huang, Jieyi Jiang, Xun Zhu, Yayue Liu, Lan Liu, Yongjun Lu, Mengfeng Li, Yongcheng Lin, and Zhigang She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
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