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1 .     nerolidol
    ÏàËÆ¶È:73.3%
Phytochemistry          1992          31          597-608
Sesquiterpene lactones and other constituents of Mikania rimachii and Mikania microptera
Jesus G. D¨ªaz, Virgil L. Goedken, Werner Herz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3,7,11-trimethyl-1,6-dodecadien-3,10,11-triol
C15H28O3     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1987          35          1109-1117
Studies on the Glycosides of Epimedium grandiflorum MORR. Var. thunbergianum (MIQ.) NAKAI. I
TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO KARASAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (rel) (1R ,2R ,3R ,6R ,7R )1,2,3,6,7-pentahydroxy-bisabol-10(11)-ene
C15H28O5     ÏàËÆ¶È:66.6%
Phytochemistry          1999          51          551-554
Highly oxygenated bisabolenes and an acetylene from Matricaria aurea
Ahmed A. Ahmed, Maha A. Abou Elela
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3¦Â,4¦Á-dihydroxy-7-epi-eudesm-11(13)-ene
C15H26O2     ÏàËÆ¶È:66.6%
Phytochemistry          1998          49          2421-2424
Eudesmane derivatives from Laggera crispata and Pluchea carolonesis
Ahmed A. Ahmed, Hesham R. El-Seedi, Ahmed A. Mahmoud, Abd El-Aziz A. El-Douski, Ibrahim F. Zeid, Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (E,1S,4S,7S,8S)-Germacru-5,10(14)-dien-1,4,8-triol
C15H26O3     ÏàËÆ¶È:66.6%
Phytochemistry          1993          34          1549-1559
Oxygenated germacranes from Santolina chamaecyparissus
J.Alberto Marco, Juan F. Sanz-cervera, Miguel Carda, Johann Lex
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     6¦Á-hydroxycyclonerolidol
    ÏàËÆ¶È:66.6%
Phytochemistry          1987          26          2854-2855
Nerolidol derivatives from Asteriscus sericeus
J. Jakupovic,L. Lehmann,F. Bohlmann,A.Arroyo Hogdson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (Z)-nerolidol
    ÏàËÆ¶È:66.6%
Magnetic Resonance in Chemistry          2005          43          176-179
Enantiomeric differentiation of acyclic terpenes by 13C NMR spectroscopy using a chiral lanthanide shift reagent
Marie-C¨¦cile Blanc, Pascale Bradesi and Joseph Casanova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3,7,11-trimethyldodec-10-en-1-ol
C15H30O     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2010          18          3116-3124
Structure¨Cactivity relationships in the conversion of vitamin K analogues into menaquinone-4. Substrates essential to the synthesis of menaquinone-4 in cultured human cell lines
Yoshitomo Suhara, Akimori Wada, Yoji Tachibana, Masato Watanabe, Kanae Nakamura, Kimie Nakagawa, Toshio Okano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (2S*,2'R*,5'S*)-2-(5'-ethenyltetrahydro-5'-methylfuran-2'-yl)-6-methylhept-5-en-2-ol
C15H26O2     ÏàËÆ¶È:66.6%
Natural product sciences          2011          17          10-13
Cytotoxic Sesquiterpenoid from the Seeds of Amomum xanthioides
Kim, Ki-Hyun; Choi, Jung-Wook; Choi, Sang-Un; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     d5-nerolidol
    ÏàËÆ¶È:66.6%
Journal of Chemical Ecology          2013          39          377-389
Steps in the Biosynthesis of Fuscumol in the Longhorn Beetles Tetropium fuscum (F.) and Tetropium cinnamopterum Kirby
Peter D. Mayo, Peter J. Silk, Michel Cusson, Catherine B¨¦liveau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Nerolidol
    ÏàËÆ¶È:66.6%
Molecules          2013          18          2166-2182
Antibacterial/Antifungal Activity and Synergistic Interactions between Polyprenols and Other Lipids Isolated from Ginkgo Biloba L. Leaves
Ran Tao, Cheng-Zhang Wang and Zhen-Wu Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     elongatol D
C15H24O4     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2007          55(5)          762-765
Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata
Shang-Kwei WANGa and Chang-Yih DUH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     1¦Â-Hydroxy-eudesma-5,11-diene
    ÏàËÆ¶È:60%
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
14 .     lanceoloxide
C15H24O     ÏàËÆ¶È:60%
Phytochemistry          2004          65          2045-2049
Sesquiterpenes from the east African sandalwood Osyris tenuifolia
Andreas Th. Kreipl, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2,6,10-trimethyl-2-undecen-6-ol
C14H28O     ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          214-218
Nuapapuin A and Sigmosceptrellins D and E: New Norterpene Cyclic Peroxides from a Southern Australian Marine Sponge, Sigmosceptrella sp.
Simon P. B. Ovenden and Robert J. Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     1,4-peroxy-muurol-5-ene
C15H24O2     ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          549-553
Muurolane Sesquiterpenes from Illicium tsangii
Koon-Sin Ngo, Wing-Tak Wong, and Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3¦Â-hydroxyilicic acid
C15H24O4     ÏàËÆ¶È:60%
Journal of Natural Products          1998          61          798-800
New Sesquiterpenoids from the Jordanian Medicinal Plant Inula viscosa
Musa H. Abu Zarga, Emad M. Hamed, Salim S. Sabri, Wolfgang Voelter, and Klaus-Peter Zeller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     zingiberene-3,6-¦Á-endoperoxide
C15H24O2     ÏàËÆ¶È:60%
Planta Medica          1996          62          565-566
Sesquiterpene Peroxides from Senecio selloi and Eupatorium rufescens
G. R¨¹cker, E. P. Scherikel, D. Manns, R. Mayer,K. Heiden, and B. M. Heinzmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     isoaminobisabolenol-b
C15H27NO     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1987          35          928-931
FOUR NEW BISABOLENE-TYPE AMINOSESQUITERPENES FROM AN OKINAWAN MARINE SPONGE, THEONELLA SP. (THEONELLIDAE)
Isao Kitagawa,Norihito Yoshioka,Chikayo Kamba,Masayuki Yoshikawa and Yoshihiro Hamamoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (+)-(2R,4S,Z)-Sesquirose oxide
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          1980          63          1589-1597
Synthesis of Enantiomeric 3-Oxa-analogues of cis-Rose Oxide and of S
Tobeastriver
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