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13C NMR (101MHz,MeOD) 23.9,30.3,33.0,34.8,35.4,47.2,50.1,54.8,59.2,62.0,77.1,79.5,92.7,117.8,159.6
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1 .     8-hydroxy-9-methoxy-¦Â-mono-cyclonerolidol
C16H28O2     ÏàËÆ¶È:56.2%
Phytochemistry          1996          43          1285-1291
Africane- and monocyclofarnesane-type sesquiterpenoids from the liverwort Porella subobtusa
Fumihiro Nagashima, Hiromi Izumo, Atsushi Ishimaru, Shiori Momasaki, Masao Toyota, Toshihiro Hashimoto, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Sch 601254
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          484-487
Caryophyllenes from a Fungal Culture of Chrysosporium pilosum
Shu-Wei Yang, Tze-Ming Chan, Joseph Terracciano, Eric Boehm, Reena Patel, Guodong Chen, David Loebenberg, Mahesh Patel, Vincent Gullo, Birendra Pramanik, and Min Chu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     crescentin IV 3-O-¦Â-D-glucopyranoside
C15H28O9     ÏàËÆ¶È:53.3%
Phytochemistry          2005          66          589-597
Further constituents from the bark of Tabebuia impetiginosa
Tsutomu Warashina, Yoshimi Nagatani, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     artemisinin G
    ÏàËÆ¶È:53.3%
Phytochemistry          2003          64          303-323
Terpenoids from the seeds of Artemisia annua
Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 7
C15H22O5     ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          184-188
Deoxyartemisinin Derivatives from Photooxygenation of Anhydrodeoxydihydroartemisinin and Their Cytotoxic Evaluation
Ahmed M. Galal,Samir A. Ross, Mahmoud A. ElSohly, Hala N. ElSohly,Farouk S. El-Feraly,Mohamed S. Ahmed, and Andrew T. McPhail
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (4R,5R,8S)-4,5:8,13-diepoxycaryophyllane
C15H24O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          41-44
Biotransformation of Caryophyllene Oxide by Botrytis cinerea
Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     decahydro-1a,4a,7,7-tetramethyl-1H-cycloprop[e]-azulene-2,5-diol (1aR,2R,4aS,5S,7aR,7bR)
C15H26O2     ÏàËÆ¶È:53.3%
Planta Medica          2005          71          979-982
Acetophenone Derivatives and Sesquiterpene from Euphorbia ebracteolata
Zhi-Qi Yin ,Chun-Lin Fan ,Wen-Cai Ye, Ren-Wang Jiang,Chun-Tao Che , Thomas C. W. Mak ,Shou-Xun Zhao,Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     [{Ce(¦Ì-OtBu)(tBuO)3]}2(¦Ì-HLS)]
C42H91Ce2N2O9     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2009          92          2291-2294
Organometallic Cerium Complexes from Tetravalent Coordination Complexes
Polly L. Arnold, Ian J. Casely, Sergey Zlatogorsky, Claire Wilson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (1R*,3S*,4S"*,5S*,9R*)-4-Hydroxymethyl-3,6,6-trimethyltricyclo[3.3.1.0 1.3]nonan-9-ol
C13H22O2     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          1980          63          1856-1866
Photochemische Reaktionen. 112. Mitteilung [1] Zur Photochemie , ¦Á,¦Â-unges?ttigter ,¦Ã,¦Ä -Epoxyester. III. Erg?nzende Untersuchungen zur Triplettreaktivit?t
Kazuo Murato, Bruno Frei, Wolfhard Bernd Schweizer, Hans Richard Wolf, Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (3aS,5aS,7S,9aR,9bR)-3a,7,8,8-Tetramethoxydecahydro-1H-cyclopentapyrano[3,2-d]pyrane
C15H26O6     ÏàËÆ¶È:53.3%
Russian Journal of Organic Chemistry          2014          50(1)          117−127
Eleuthesides and Their Analogs: V.* Medium- and Large-Ring Lactones Based on Levoglucosenone
Yu. A. Khalilova, L. V. Spirikhin, Sh. M. Salikhov, and F. A. Valeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 11
    ÏàËÆ¶È:53.3%
Phytochemistry          1990          29          757-763
Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes
Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ethyl cis-4-(cyanomethyl)-N-allyl-piperidine-2-carboxylate
C13H20N2O2     ÏàËÆ¶È:53.3%
Journal of Medicinal Chemistry          1991          34          90-97
4-(Tetrazolylalkyl)piperidine-2-carboxylic acids. Potent and selective N-methyl-D-aspartic acid receptor antagonists with a short duration of action
Paul L. Ornstein, Darryle D. Schoepp, M. Brian Arnold, J. David Leander, David Lodge, Jonathan W. Paschal, Tom Elzey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 12
C13H22O2     ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          1989          1989          1195-1201
Epoxytetrahydroedulan, a New Terpenoid from the Hairpencils of Euploea (Lep.: Danainae) Butterflies
Wittko Francke, Stefan Schulz, Volker Sinnwell, Wilfried A. König and Yves Roisin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     13-hydroxy-elviranol
C15H26O3     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2014          62          1192-1199
A Rare Type of Sesquiterpene and ¦Â-Santalol Derivatives from Santalum album and Their Cytotoxic Activities
Yukiko Matsuo, Hiroshi Sakagami, Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     9b-Acetoxy artemisinin
C17H24O7     ÏàËÆ¶È:52.9%
Bioorganic & Medicinal Chemistry Letters          2010          20          359-361
Bio-transformation of artemisinin using soil microbe: Direct C-acetoxylation of artemisinin at C-9 by Penicillium simplissimum
Abhishek Goswami, Partha P. Saikia, Nabin C. Barua, Manobjyoti Bordoloi, Archana Yadav, Tarun C. Bora, Binod K. Gogoi, Ajit Kumar Saxena, Nithasa Suri, Madhunika Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 5a
C18H33O4P     ÏàËÆ¶È:52.9%
Archives of Pharmacal Research          2000          23          206-210
Synthesis and biological evaluation of phosphonate analogues of 1¦Á, 25-dihydroxyvitamin D3
Gyoonhee Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     17¦Â-hydroxyandrost-4-ene-3,11-dione
C19H26O3     ÏàËÆ¶È:52.6%
Natural Product Research          2002          16          345-349
Microbial Transformation of (+)-Adrenosterone
S. Ghulam Musharraf; Atta-Ur-Rahman; M. Iqbal Choudhary; Sadia Sultan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1 -methyldeacetyldeformyl-1 ,2-dihydroakuammiline
    ÏàËÆ¶È:50%
Planta Medica          1989          55          188-190
New Quaternary Alkaloids from Vinca minor
B. Proksa, D. UhrIn, F. Grossmann, and Z. Voticky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Angustifoline N-carboxyethyl ester
    ÏàËÆ¶È:50%
Phytochemistry          1992          31          4343-4345
Lupin alkaloids from Lupinus polyphyllus
Gerhard Veen, Claudia Schmidt, Ludger Witte, Victor Wray, Franz-Christian Czygan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 4a
C24H47O4PSi     ÏàËÆ¶È:50%
Archives of Pharmacal Research          2000          23          206-210
Synthesis and biological evaluation of phosphonate analogues of 1¦Á, 25-dihydroxyvitamin D3
Gyoonhee Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound E2-4
    ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          1998          36          779-796
13C NMR spectroscopy of tri- and tetracyclic quinolizidine alkaloids. Compilation and discussion
B. Mikhova and H. Duddeck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     N(a)-Methyl Deacetyldeformyl-1,2-dihydroakuammiline
    ÏàËÆ¶È:50%
The Journal of Organic Chemistry          1977          42          2785-2786
Structure analysis by carbon-13 nuclear magnetic resonance spectroscopy of pleiocraline, a new bisindole alkaloid from Alstonia deplanchei van Heurck et Muell. Arg
Bhupesh C. Das, Jean Pierre Cosson, Gabor Lukacs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Huperserine A
C16H23NO2     ÏàËÆ¶È:50%
Fitoterapia          2014          99          72-77
Huperserines A¨CE, Lycopodium alkaloids from Huperzia serrata
Wei-Wei Jiang, Fei Liu, Xiu Gao, Juan He, Xiao Cheng, Li-Yan Peng, Xing-De Wu, Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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