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1.  17.275,17.791,26.018,27.429,29.767,31.337,33.971,41.279,44.967,112.159,138.599,146.181,170.670,208.736,209.176

2.
15.598,20.341,21.950,23.028,25.297,28.628,29.531,42.068,46.728,49.445,55.743,57.026,73.054,211.430

3.  16.304,17.564,32.840,35.451,59.348,75.520,111.188,123.573,139.449,147.334

4.
18.247,22.625,31.269,33.090,63.196,80.825,84.657,110.634,144.883
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1 .     4,5-seco-Guaia-1(10),11-diene-4,5-dioxo
C15H22O2     ÏàËÆ¶È:100%
Tetrahedron          2011          67          9193-9198
Sesquiterpenoids, alantolactone analogues, and seco-guaiene from the roots of Inula helenium
Hai-Long Jiang, Jia Chen, Xiao-Jie Jin, Jun-Li Yang, Ya Li, Xiao-Jun Yao , Quan-Xiang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     mandassidione
C15H22O2     ÏàËÆ¶È:100%
Phytochemistry          1988          27          3319-3321
Mandassidione and other sesquiterpenic ketones from Cyperus articulatus
B. Nyasse,R. Ghogomu,Tih B.L. Sondengam,M. T. Martin,B. Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     cyperusol B1
C15H24O2     ÏàËÆ¶È:80%
Journal of Natural Products          2004          67          569-576
Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus
Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     mandassidione
     ÏàËÆ¶È:80%
China Journal of Chinese Materia Medica          2010          35          315-322
Terpenoids of Heteroplexis micocephala and their bioactivities
FAN Xiaona; LIN Sheng; ZHU Chenggen; HU Jinfeng; LIU Yang; CHEN Xiaoguang; CHEN Naihong; WANG Wenjie; SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     cyperusol B2
C15H24O2     ÏàËÆ¶È:73.3%
Journal of Natural Products          2004          67          569-576
Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus
Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     10-epi-Acora-3,11-dien-15-ol
     ÏàËÆ¶È:66.6%
Flavour and Fragrance Journal          2000          15          61-83
1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil
Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Huperzine W
C14H21NO2     ÏàËÆ¶È:60%
Chinese Chemical Letters          2002          13          331-332
Huperzine W, a Novel 14 Carbons Lycopodium Alkaloid from Huperzia serrata
Chang Heng TAN, Xiao Qiang MA, Guo Fu CHEN, Shan Hao JIANG,Da Yuan ZHU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     4 (15)-cadinene-6,10-diol
C23H24O11     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2004          6          199-204
CHEMICAL CONSTITUENTS FROM ALPINIA TONKINENSIS
JIAN ZHANG and LING-YI KONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (-)-huperzine W
C14H21NO2     ÏàËÆ¶È:60%
Natural Products and Bioprospecting          2012          2          255-257
One-step synthesis of Lycopodium alkaloid (-)-huperzine W via Suzuki-Miyaura coupling
Tao Xu, Shi-Zhi Jiang, Huai-Rong Luo, Yu-Rong Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (1S,6R,7S,10S)-7-isopropyl-10-methyl-4-methylenedecahydronaphthalene-6,10-diol
C15H26O2     ÏàËÆ¶È:60%
Acta Crystallographica Section E          2007          63          o3579
6¦Â,10¦Â-Cadinene-6,10-diol: a sesquiterpenoid from the rhizome of Acorus calamus L.
Wei-Wei Dong, Kai-Bei Yu, Jian-Min Yue and Run-Hua Lu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-14 09:58:54
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1 .     compound E
     ÏàËÆ¶È:100%
Phytochemistry          1989          28          1425-1426
Sesquiterpenes from Eremophila species
Kim A. Dastlik,Peter G. Forster,Emilio L. Ghisalberti,Phillip R. Jefferies
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     oplopanone
     ÏàËÆ¶È:100%
Archives of Pharmacal Research          1997          20          363-367
Sesquiterpene components from the flower buds of Magnolia fargesii
Keun Young Jung, Dong Seon Kim, Sei Ryang Oh, Im Seon Lee and Jung Joon Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ent-oplopanone
C15H26O2     ÏàËÆ¶È:93.3%
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

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4 .     oplopanone
C15H26O4     ÏàËÆ¶È:93.3%
Natural Product Research          2003          17          445-449
A new xanthone from Hedychium gardnerianum
Maria João Carvalho; Lu¨ªs M. Carvalho; Ana Margarida Ferreira; Artur M. S. Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (-)-oplopanone
     ÏàËÆ¶È:93.3%
China Journal of Chinese Materia Medica          2009          34          990-993
Studies on chemical constituents in fruit of Alpinia oxyphylla
XU Junju, TAN Ninghua, ZENG Guangzhi, HAN Hongjin, HUANG Huoqiang, JI Changjiu, ZHU Meiju, ZHANG Yumei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     oplopanone
C15H26O2     ÏàËÆ¶È:93.3%
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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7 .     Oplopanone
     ÏàËÆ¶È:93.3%
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

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8 .     Oplopanone
     ÏàËÆ¶È:93.3%
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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9 .     oplopanone
     ÏàËÆ¶È:93.3%
Phytochemistry          1983          22          1457-1459
Sesquiterpene alcohols and triterpenoids from Liatris microcephala
Werner Herz, Kinzo Watanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     oplopanone
     ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2009          40          29-32
ÒæÖÇÈÊ»¯Ñ§³É·ÖÑо¿
Áõéª;ÓÚÐÂÓî;ÕÔºì;ÕÔÓàÇì
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Oplopanone
     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2008          6          339-341
Sesquiterpenes from the Stems of Croton caudatus Geisel. var. tomentosus Hook.
WANG Yuan; ZOU Zhong-Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     Oplopanone
     ÏàËÆ¶È:93.3%
Archives of Pharmacal Research          2010          33          1317-1323
Scopoletin from the flower buds of Magnolia fargesii inhibits protein glycation, aldose reductase, and cataractogenesis Ex Vivo
Jun Lee, Nan Hee Kim, Joo Won Nam, Yun Mi Lee and Dae Sik Jang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     oplopanone
     ÏàËÆ¶È:93.3%
Journal of the Chinese Chemical Society          2002          49          427-431
Cytotoxic Components from the Leaves of Schefflera taiwaniana
Yueh-Hsiung Kuo*, Jir-Mehng Lo and Yih-Fwu Chan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     oplopanone
     ÏàËÆ¶È:93.3%
Journal of the Chinese Chemical Society          2005          52          369-374
Terpenoids from the Flower of Cacalia tangutica
Xia Liu, Quan-Xiang Wu and Yan-Ping Shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     subdigitatone
C15H26O2     ÏàËÆ¶È:93.3%
Indian Journal of Chemistry          1995          34B          664-665
New sesquiterpene from Artemisia subdigitata
Yu Li, Yanping Shi & Yang Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-10-14 09:59:49
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1 .     (6RS)-(E)-3,7-Dimethyl-2,7-octadiene-1,6-diol
     ÏàËÆ¶È:100%
Journal of Agricultural and Food Chemistry          1998          46          1966-1970
(S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals of Rosa damascena Mill.
Holger Knapp, Markus Straubinger, Selenia Fornari, Noriaki Oka, Naoharu Watanabe, and Peter Winterhalter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 25
     ÏàËÆ¶È:90%
Organic Magnetic Resonance          1975          7          426-432
13C-NMR-Spektren von Monoterpenen
F. Bohlmann, R. Zeisberg and E. Klein
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (3S)-(E)-2,6-dimethyl-10-methylene-1,6,11-dodecatrien-3-ol
     ÏàËÆ¶È:60%
Journal of Natural Products          1992          Vol 55          428
New Farnesane Sesquiterpenes from Hebeloma senescens
Maurizio Bocchi, Luigi Garlaschelli, Giovanni Vidari, Giorgio Mellerio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 2
C10H14O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2009          57          294-297
Structure of New Monoterpene Glycoside from Sibiraea angustata RCHD. and Its Anti-obestic Effect
Yoshiaki Ito, Satoshi Kamo, Samir Kumar Sadhu, Takashi Ohtsuki, Masami Ishibashi and Yoshihiro Kano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 10f
C10H10N4O2     ÏàËÆ¶È:60%
Journal of Heterocyclic Chemistry          2000          37          1041-1048
Reactivity studies of ethyl(Z)-N-(2-amino-1,2-dicyanovinyl) formimidate with carbonyl compounds in the presence of base
M. Jos¨¦alves, M. Alice Carvalho, M. Fernanda, J. R. P. Proença and Brian L. Booth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (2Z)-2,6-dimethylhepta-2,6-diene-1,5-diol
     ÏàËÆ¶È:60%
Russian Journal of Organic Chemistry          2011          47          1287-1292
Synthesis of 6-hydroxycarvone derivatives and their oxidative decyclization with lead tetraacetate
R. F. Valeev, R. F. Bikzhanov, N. K. Selezneva, F. A. Gimalova and M. S. Miftakhov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (7RS)-(2E)-3,7-Dimethyl-2-octene-1,8-diol
     ÏàËÆ¶È:60%
Journal of Agricultural and Food Chemistry          1998          46          1966-1970
(S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals of Rosa damascena Mill.
Holger Knapp, Markus Straubinger, Selenia Fornari, Noriaki Oka, Naoharu Watanabe, and Peter Winterhalter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (7RS)-(2Z)-3,7-Dimethyl-2-octene-1,8-diol
     ÏàËÆ¶È:60%
Journal of Agricultural and Food Chemistry          1998          46          1966-1970
(S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals of Rosa damascena Mill.
Holger Knapp, Markus Straubinger, Selenia Fornari, Noriaki Oka, Naoharu Watanabe, and Peter Winterhalter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     5-(3-Furyl)-2-methyl-1-pentene-3-ol
     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          1992          1992          279-281
Terpenes and Terpene Derivatives, XXVIII. New Monoterpene Derivatives from the Essential Oil of Artemisia salsoloides
Peter Weyerstahl, Hans-Christian Wahlburg, Vijay K. Kaul and Stanislaw Lochynski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Tolbutamide
     ÏàËÆ¶È:60%
Applied Microbiology and Biotechnology          2006          72          486-491
Biotransformation of tolbutamide to 4¡ä-hydroxytolbutamide by the fungus Cunninghamella blakesleeana
Haihua Huang, Xiuwei Yang, Qiang Li, Lu Sun, Dafang Zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2013-10-14 10:00:35
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1 .     5,6-epoxy-5-isopropyl-6-methyl-hepy-3-in-2-on
C11H16O2     ÏàËÆ¶È:60%
Helvetica Chimica Acta          1977          60          743-767
Photochemische Reaktionen. 93. Mitteilung. Zur Photochemie konjugierter Epoxy-inone: Die UV.-Bestrahlung von 5,6-Epoxy-5-isopropyl-6-methyl-hept-3-in-2-on
Herbert Eichenberger, Hans Richard Wolf and Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (Z)-6-hydroxymethyl-2-methylocta-1,6-diene-3,8-diol
C10H18O3     ÏàËÆ¶È:60%
Australian Journal of Chemistry          1989          42          1983-1993
Tropical Marine-Algae. VI. New Monoterpenes From Several Collections of Chondrococcus hornemannii (Rhodophyta, Gigartinales, Rizophyllidaceae)
JC Coll and AD Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     compound 8a
     ÏàËÆ¶È:55.5%
Zeitschrift f¨¹r Naturforschung B          2007          62          1174-1182
Triethylborane: An "Old" Reagent with New Functions. 1,2-Hydroboration
B. Wrackmeyer, E. Khan, S. Bayer, and K. Shahid
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound
C8H14O     ÏàËÆ¶È:55.5%
Journal of the American Chemical Society          2004          126          14720-14721
Total Synthesis of Kendomycin:  A Macro−C−Glycosidation Approach
Yu Yuan, Hongbin Men, and Chulbom Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 21'
C9H18O3     ÏàËÆ¶È:55.5%
Tetrahedron          2012          68          8994-9003
Enantiodivergent synthesis of (+)- and (−-isolaurepan
Gonzalo Pazos, Manuel P¨¦rez, Zoila G¨¢ndara, Generosa G¨®mez, Yagamare Fall
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     4-nonyn-1-ol
     ÏàËÆ¶È:55.5%
Journal of Chemical Ecology          2010          36          923-932
Identification of the Sex Pheromone of a Protected Species, the Spanish Moon Moth Graellsia isabellae
Jocelyn G. Millar, J. Steven McElfresh, Carmen Romero, Marta Vila, Neus Mar¨ª-Mena, Carlos Lopez-Vaamonde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     4-Isopropyl-2,7-dimethyl-3-oxa-1.4.7-octatrien
C12H20O     ÏàËÆ¶È:54.5%
Helvetica Chimica Acta          1981          64          198-214
Photochemische Reaktionen. 117. Mitteilung [1] Zur Photochemie von 5,6-Epoxydienen und konjugierten 5,6-Epoxytrienen
Alex Peter Alder, Hans Richard Wolf, Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     7-dodecyn-1-ol
     ÏàËÆ¶È:54.5%
Journal of Chemical Ecology          2006          32          1085-1099
Isolation, Identification, Synthesis, and Field Evaluation of the Sex Pheromone of the Brazilian Population of Spodoptera frugiperda
Luciane G. Batista-Pereira, Kathrin Stein, Andr¨¦ F. de Paula, Jardel A. Moreira, Ivan Cruz, Maria de Lourdes C. Figueiredo, Jos¨¦ Perri Jr., Arlene G. Corr¨ºa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     masutakic acid A
C10H16O4     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2001          49(3)          327-329
A Benzofuran Glycoside and an Acetylenic Acid from the Fungus Laetiporus sulphureus var. miniatus
Kazuko YOSHIKAWA, Shinya BANDO,Shigenobu ARIHARA,Eiko MATSUMURA,and Satoshi KATAYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (2R,3R,4R)-5-Chrysanthemen-1,4-diol
C10H18O2     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          37-41
Polyoxygenated Eudesmanes and trans-Chrysanthemanes from the Aerial Parts of Santolina insularis
Ernesto Fattorusso, Federico U. Santelia, Giovanni Appendino, Mauro Ballero, and Orazio Taglialatela-Scafati
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     jatamanin F
C10H16O4     ÏàËÆ¶È:50%
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

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12 .     2-butyl-5-ethynyltetrahydrofuran(Minor isomer)
C10H16O     ÏàËÆ¶È:50%
Organic Letters          2007          Vol. 9, No. 10          1975-1978
Ene-yne Tetrahydrofurans from the Sponge Xestospongia muta. Exploiting a Weak CD Effect for Assignment of Configuration
Brandon I. Morinaka, Colin K. Skepper, and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     2Z,4E-decadienoic methyl ester
     ÏàËÆ¶È:50%
Phytochemistry          1988          27          207-212
Diterpenes from the latex of Euphorbia broteri
Julio Gonz¨¤lez Urones,Pilar Basabe Barcala,Ma Jos¨¨ Sexmero Cuadrado,Isidro S¨¤nchez Marcos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     2,2,8,8-tetrahexyl-3,6,9-trioxaundecane-1,11-diol
     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2001          38          1259-1264
Synthesis of new proton-ionizable crown ether compounds containing substituted lh-pyridin-4-one subcyclic units
Peter Huszthy, Julia Kertesz, Jerald S. Bradshaw, Reed M. Izatt and J. Ty Redd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (S)-1-((3R,5R,S)-5-Methyl-5-(2-((triisopropylsilyl) oxy)ethyl)-1,2-dioxolan-3-yl)ethane-1,2-diol
C17H36O5Si     ÏàËÆ¶È:50%
Tetrahedron          2012          68          3717-3724
Exploratory studies toward the synthesis of the peroxylactone unit of plakortolides
Bogdan Barnych, Jean-Michel Vat¨¨le
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     1-(2'-(1''-hydroxy-1''-methylethyl)thien-3'-ylmethyl)-3,3,4,4-tetramethylsuccinimide
C16H23NO3S     ÏàËÆ¶È:50%
Heterocycles          2001          54          275-282
Azepine and [1,3]Oxazepine Fused Ring Construction through a Cationic Cyclization: an N-acyliminium Ion Trapping of an Oxygen Atom or Olefin
Aïcha Mamouni, Adam Daïch, Stefan Marchalin, and Bernard Decroix
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     2-(2-methoxyethoxy)-5-methyl-5-hexen-2-yl hydroperoxide
     ÏàËÆ¶È:50%
Heterocycles          2000          53          1293-1304
Synthesis of 3-Hydroperoxy (or Hydroxy)-substituted 1,2-Dioxanes and 1,2-Dioxepanes by the Ozonolysis of Unsaturated Hydroperoxy Acetals
Takahiro Tokuyasu, Toyonari Ito, Araki Masuyama, and Masatomo Nojima*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     5-isopropenyl-2-methyltetrahydrofuran-2-acetaldehyde
C10H16O2     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2002          38          1594-1605
Transformations of 6,7-Epoxy Derivatives of Citral and Citronellal in Various Acidic Media
O. I. Yarovaya, O. V. Salomatina, D. V. Korchagina, M. P. Polovinka and V. A. Barkhash
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     N,5-bis(tert-butyldimethylsilyloxy)pentanamide
C17H39NO3Si2     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2011                   2293-2300
Glucosinolate Synthesis: a Hydroxamic Acid Approach
Deimante Cerniauskaite, Jolanta Rousseau, Algirdas Sackus, Patrick Rollin and Arnaud Tatibouët
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     9-tetradecyn-1-ol
     ÏàËÆ¶È:50%
Journal of Chemical Ecology          2006          32          1085-1099
Isolation, Identification, Synthesis, and Field Evaluation of the Sex Pheromone of the Brazilian Population of Spodoptera frugiperda
Luciane G. Batista-Pereira, Kathrin Stein, Andr¨¦ F. de Paula, Jardel A. Moreira, Ivan Cruz, Maria de Lourdes C. Figueiredo, Jos¨¦ Perri Jr., Arlene G. Corr¨ºa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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