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13C NMR (101 MHz, Acetone) ¦Ä 147.77, 144.72, 131.06, 128.72, 124.79, 121.60, 117.74, 111.88, 74.85, 64.98, 39.68, 39.19, 37.31, 37.22, 37.14, 37.08, 32.60, 32.47, 31.46, 27.77, 24.59, 24.19, 23.54, 22.07, 22.04, 21.99, 20.73, 19.18, 19.15, 18.95, 13.07, 11.18, 11.13
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1 .     ¦Á-tocopherol
C29H52O2     ÏàËÆ¶È:78.7%
Chemical & Pharmaceutical Bulletin          1998          46          1647-1649
Constituents of Ficus pumila Leaves
Junichi KITAJIMA,Kaoru KIMIZUKA,Masanobu ARAI and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     ¦Á-tocopherol
    ÏàËÆ¶È:78.7%
Korean Journal of Pharmacognosy          2008          39(1)          28-36
Phytochemical Studies on Paeoniae Radix (2);Phenolic and Related compounds
Kim, Ju-Sun; Kim, Yoon-Jung; Lee, Joo-Young; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     ¦Á-tocopherol
    ÏàËÆ¶È:78.7%
Journal of the Chinese Chemical Society          2000          47          555-560
The Chemical Constituents from the Heartwood of Eucalyptus citriodora
Ching-Kuo Lee* and Ming-Huey Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     ¦Á-Tocopherol
    ÏàËÆ¶È:75.7%
Archives of Pharmacal Research          2002          25          628-635
Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines
Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     5-nitro-¦Ã-tocopherol
C28H47O4N     ÏàËÆ¶È:75.7%
Bioorganic & Medicinal Chemistry          2011          19          6483-6491
Tocotrienamines and tocopheramines: Reactions with radicals and metal ions
Francesco Galli, Francesco Mazzini, Luca Bamonti, Lars Gille, Stefan Böhmdorfer, Marta Piroddi, Thomas Netscher, Frank J. Kelly, Thomas Rosenau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     3,4-dehydro-¦Á-tocopherol
C29H48O2     ÏàËÆ¶È:72.7%
Phytochemistry          2004          65          2719-2729
Antioxidant dehydrotocopherols as a new chemical character of Stemona species
Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     ¦Á-ÉúÓý·Ó
C29H50O2     ÏàËÆ¶È:72.7%
Journal of Shenyang Pharmaceutical University          2003          20          425-427
Chemical constituents of Pyrrosia petiolosa(Christ) Ching
WANG Nan, WANG Jin-hui, CHENG Jie, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     7a-methoxy-¦Á-tocopherol
C30H52O3     ÏàËÆ¶È:72.7%
Journal of the Chinese Chemical Society          2007          54          41-45
Tocopherols and Triterpenoids from Sida acuta
Chiy-Rong Chen, Li-Hui Chao, Min-Hsiung Pan,Yun-Wen Liao and Chi-I Chang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     preunusol A
C37H54O4     ÏàËÆ¶È:72.7%
Agricultural and Biological Chemistry          1991          55          1727-1731
Prunusols A and B, Novel Antioxidative Tocopherol Derivatives Isolated from the Leaf Wax of Prunus grayana Maxim.
Toshihiko OSAWA, Shigenori KUMAZAWA, Shunro KAWAKISHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     (+)-¦Á-Tocopheryl ¦Á-D-glucopyranoside
    ÏàËÆ¶È:70.5%
Zeitschrift f¨¹r Naturforschung B          2002          57          571-578
Studies in the Acid Catalysed Glycosylation of a-Tocopherol
S. Witkowski and P. Wa£jko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     isomeric 3,4-dehydro-¦Â-tocopherol
C28H46O2     ÏàËÆ¶È:69.6%
Phytochemistry          2004          65          2719-2729
Antioxidant dehydrotocopherols as a new chemical character of Stemona species
Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     dehydro-¦Ã-tocopherol
C28H46O2     ÏàËÆ¶È:69.6%
Phytochemistry          2004          65          2719-2729
Antioxidant dehydrotocopherols as a new chemical character of Stemona species
Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyl-12-tridecenyl)-2H-1-benzopyran-6-ol
    ÏàËÆ¶È:69.6%
Journal of Natural Products          1999          62          1685-1687
A New Vitamin E (¦Á-Tocomonoenol) from Eggs of the Pacific Salmon Oncorhynchus keta
Yorihiro Yamamoto, Nobuo Maita, Akio Fujisawa, Junko Takashima, Youichi Ishii, and Walter C. Dunlap
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     2,5-dimethyl-2-(4,8,12-trimethyltridecyl)naphtho[1,2-b]-3,4-dihydro-2H-pyran-6-yl (tert-butyloxycarbonyl)amino]acetate
C38H59NO5     ÏàËÆ¶È:69.6%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     preunusol B
    ÏàËÆ¶È:69.6%
Agricultural and Biological Chemistry          1991          55          1727-1731
Prunusols A and B, Novel Antioxidative Tocopherol Derivatives Isolated from the Leaf Wax of Prunus grayana Maxim.
Toshihiko OSAWA, Shigenori KUMAZAWA, Shunro KAWAKISHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     dehydro-¦Ä-tocopherol
C27H44O2     ÏàËÆ¶È:66.6%
Phytochemistry          2004          65          2719-2729
Antioxidant dehydrotocopherols as a new chemical character of Stemona species
Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     compound 24¦Á-1b
    ÏàËÆ¶È:66.6%
Phytochemistry          1988          27          1161-1164
Triterpenoids from the rhizome of Alisma plantago-aquatica
Geng Pei-Wu,Yoshiyasu Fukuyama,Toshihide Yamada,Wang Rei,Bao Jinxian,Kazuyuki Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     compound 24¦Â-1b
    ÏàËÆ¶È:66.6%
Phytochemistry          1988          27          1161-1164
Triterpenoids from the rhizome of Alisma plantago-aquatica
Geng Pei-Wu,Yoshiyasu Fukuyama,Toshihide Yamada,Wang Rei,Bao Jinxian,Kazuyuki Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     (+)-¦Á-Tocopheryl 2,3,4,6-tetra-O-acetyl--D-galactopyranoside
    ÏàËÆ¶È:66.6%
Zeitschrift f¨¹r Naturforschung B          2002          57          571-578
Studies in the Acid Catalysed Glycosylation of a-Tocopherol
S. Witkowski and P. Wa£jko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     24-ethyl-¡÷5,22-sterol acetate
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          1999          11(5)          8-10
STUDY ON THE CHEMICAL CONSTITUENTS OF CLERODENDRON BUNGEI STEUD
Dong Xiaoping; Qiao Rongxia; Guo Li; Xie Jie; Liu Bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     2,5-dimethyl-2-(4,8,12-trimethyltridecyl)naphtho[1,2-b]-3,4-dihydro-2H-pyran-6-yl [(benzyloxycarbonyl)amino]acetate
C41H57NO5     ÏàËÆ¶È:64.8%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     24-ethylcholesta-5,22E-dien-3¦Â-ol
    ÏàËÆ¶È:64.7%
Phytochemistry          1988          27          1161-1164
Triterpenoids from the rhizome of Alisma plantago-aquatica
Geng Pei-Wu,Yoshiyasu Fukuyama,Toshihide Yamada,Wang Rei,Bao Jinxian,Kazuyuki Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     24-ethylcholesta-5,22E-dien-3¦Â-ol
    ÏàËÆ¶È:64.7%
Phytochemistry          1988          27          1161-1164
Triterpenoids from the rhizome of Alisma plantago-aquatica
Geng Pei-Wu,Yoshiyasu Fukuyama,Toshihide Yamada,Wang Rei,Bao Jinxian,Kazuyuki Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     2-[2'(E)-3',7',11',15'-Tetramethylhexadec-2-en-1'-yl]-6-methyl-1,4-benzohydroquinone diacetate
C31H50O4     ÏàËÆ¶È:63.6%
Phytochemistry          2009          70          1315-1320
An unusual halogenated meroditerpenoid from Stypopodium flabelliforme: Studies by NMR spectroscopic and computational methods
Carlos Areche, Aurelio San-Mart¨ªn , Juana Rovirosa, Jorge Soto-Delgado, Renato Contreras
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     (+)-¦Á-Tocopheryl ¦Á-D-mannopyranoside
    ÏàËÆ¶È:63.6%
Zeitschrift f¨¹r Naturforschung B          2002          57          571-578
Studies in the Acid Catalysed Glycosylation of a-Tocopherol
S. Witkowski and P. Wa£jko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     ¦Á-tocopherylquinone
C29H50O3     ÏàËÆ¶È:63.6%
European Journal of Organic Chemistry          2011                   3036-3049
Bromination of Tocopherols: Oxidative Halogenations and Rearrangements
Stefan Böhmdorfer, Anjan Patel, Andreas Hofinger, Thomas Netscher, Lars Gille and Thomas Rosenau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     2-bromo-¦Ã-tocopherylquinone
C28H47BrO3     ÏàËÆ¶È:63.6%
European Journal of Organic Chemistry          2011                   3036-3049
Bromination of Tocopherols: Oxidative Halogenations and Rearrangements
Stefan Böhmdorfer, Anjan Patel, Andreas Hofinger, Thomas Netscher, Lars Gille and Thomas Rosenau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     (+)-¦Á-Tocopheryl ¦Â-D-galactopyranoside
    ÏàËÆ¶È:61.7%
Zeitschrift f¨¹r Naturforschung B          2002          57          571-578
Studies in the Acid Catalysed Glycosylation of a-Tocopherol
S. Witkowski and P. Wa£jko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     4-((3R,7R,11R)-3-benzoxy-3,7,11,15-tetramethylhexa-dec-1-ynyl)-1,6-dimethyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-5-carbaldehyde
C37H54N2O2     ÏàËÆ¶È:61.7%
Bioorganic & Medicinal Chemistry          2010          18          7628-7638
Design, synthesis, and evaluation of an ¦Á-tocopherol analogue as a mitochondrial antioxidant
Jun Lu, Omar M. Khdour, Jeffrey S. Armstrong, Sidney M. Hecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     5-oxo-5-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]pentanoic acid
C34H54O4     ÏàËÆ¶È:61.7%
Molecules          2011          16          9340-9356
Communication: Consecutive Three-Component Synthesis of 3-(Hetero)Aryl-1H-pyrazoles with Propynal Diethylacetal as a Three-Carbon Building Block
Lucilla Levi, Christina Boersch, Charlotte F. Gers, Eugen Merkul and Thomas J. J. M¨¹ller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     (22R,23R,24S)-2¦Â-acetyloxy-22,23-isopropylidene-dioxy-ergost-5-ene
C33H54O4     ÏàËÆ¶È:60.6%
Phytochemistry          2001          58          343-349
Synthesis and biological activity of 26-norbrassinolide,26-norcastasterone and 26-nor-6-deoxocastasterone
Tsuyoshi Watanabe, Takahiro Noguchi, Takao Yokota, Kyomi Shibata,Hiroyuki Koshino, Hideharu Seto, Seong-Ki Kim, Suguru Takatsuto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     compound 2
    ÏàËÆ¶È:60.6%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     stigmasterol
    ÏàËÆ¶È:60.6%
China Journal of Chinese Materia Medica          1993          18          102-103
Studies on Chemical Constituents of Emilia sonchifolia L. DC
Gao Jianjun and Cheng Dongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     ¦Á-tocopherylquinone
    ÏàËÆ¶È:60.6%
Phytochemistry          1990          29          2223-2228
Terpenoid compounds from Parentucellia latifolia
J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     Progesterone-3-(6-FMO)
    ÏàËÆ¶È:60.6%
Steroids          1999          64          283-290
O-(Fluoresceinylmethyl)hydroxylamine(OFMHA): a reagent for the preparation of fluorescent O-(fluoresceinylmethyl)oxime(FMO)- steroid conjugates
Maciej Adamczyk, Yon-Yih Chen, Jonathan Grote, Phillip G. Mattingly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     compound 2b
    ÏàËÆ¶È:60.6%
Steroids          1999          64          385-395
An improved synthesis of(20R,22R)-cholest-5-ene-3¦Â,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXR¦Á
Benfang Ruan, William K. Wilson, George J. SchroepferJr.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     3 ¦Â,7¦Á-Cholest-5-ene-3,7-diol-3-benzoate
C34H50O3     ÏàËÆ¶È:60.6%
Steroids          1995          60          290-294
A convenient synthesis of 7¦Á-hydroxycholest-4-en-3-one by the hydroxypropyl-¦Â-cyclodextrin-facilitated cholesterol oxidase oxidation of 3¦Â,7¦Á-cholest-5-ene-3,7-diol
David L. Alexander, Jed F. Fisher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

38 .     1-Benzofuro[2',3':2,3]-5¦Á-cholest-2-ene
C33H48O     ÏàËÆ¶È:60.6%
Journal of the Chemical Society, Perkin Transactions 1          2000                   453-461
Synthesis and circular dichroism of steroids with 2,3-dihydro-1-benzofuran and 4H-benzopyran chromophores; revision of the absolute configuration of some norneolignans from Krameria cystisoides
Tibor Kurt¨¢n, Eszter Baitz-G¨¢cs, Zsuzsa Majer and S¨¢ndor Antus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     Stigmast-5-en-3¦Á,26-diacetate
C29H50O2     ÏàËÆ¶È:60.6%
Bulletin of the Korean Chemical Society          2006          27          93-98
New Stigmastane Steroids Constituents from Rice Hulls of Oryza sativa and Inhibitory Activity on Radish seed
Ill-Min Chung, Mohd Ali, Tran Dang Khanh, Myoung Gun Choung, Hong Jae Park, Ateeque Ahmad*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

40 .     4-oxo-4-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]butanoicacid
C33H52O4     ÏàËÆ¶È:60.6%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     4-oxo-4-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]butanoic acid
C33H52O4     ÏàËÆ¶È:60.6%
Molecules          2011          16          9340-9356
Communication: Consecutive Three-Component Synthesis of 3-(Hetero)Aryl-1H-pyrazoles with Propynal Diethylacetal as a Three-Carbon Building Block
Lucilla Levi, Christina Boersch, Charlotte F. Gers, Eugen Merkul and Thomas J. J. M¨¹ller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     2,5-dimethyl-2-(4,8,12-trimethyltridecyl)naphtho[1,2-b]-3,4-dihydro-2H-pyran-6-yl aminoacetate
    ÏàËÆ¶È:60.6%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     ergosta-5-ene-3¦Â-ol
    ÏàËÆ¶È:60.6%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2002          41(6)          36-37
Studies on the Secondary Metabolites of the Soft Coral Sinularia grayi Tix1-Dur1
MA Xiang-quan, ZHANG Guang-wen, SU Jing-yu, ZENGLong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     calocedimer B
C35H54O     ÏàËÆ¶È:60%
Journal of Natural Products          2006          69          665-667
Calocedimers A, B, C, and D from the Bark of Calocedrus macrolepis var. formosana
Chin-Lin Hsieh, Lung-Lin Shiu, Mei-Huims Tseng, Yi-Yuan Shao, and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     3b(2-p-tolyolsulfonyloxy)-ethoxycholest-5-ene
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          2010          20          2872-2875
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     4-((3R,7R,11R)-3-benzoxy-3,7,11,15-tetramethylhexadec-1-ynyl)-2,3-dihydro-1,6-dimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl acetate
C38H56N2O3     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2010          18          7628-7638
Design, synthesis, and evaluation of an ¦Á-tocopherol analogue as a mitochondrial antioxidant
Jun Lu, Omar M. Khdour, Jeffrey S. Armstrong, Sidney M. Hecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

47 .     daucosterol
    ÏàËÆ¶È:60%
Natural Product Research and Development          1997          9(4)          10-13
CHEMICAL INVESTIGATION OF MORINA CHINESIS
Zhang Guolin; Zhou Zhengzhi; Li Bogang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     mixture of ¦Â-sitosterol and stigmasterol
    ÏàËÆ¶È:60%
Food Chemistry          2011          127          394-403
Chemical composition and biological activity of Citrus jambhiri Lush
Dalia Hamdan, Mahmoud Zaki El-Readi, Ahmad Tahrani, Florian Herrmann, Dorothea Kaufmann, Nawal Farrag, Assem El-Shazly, Michael Wink
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     5-(2,5-difluorophenyl)-2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-chroman-6-yl acetate
    ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2011                   2450-2457
Synthesis of 5-(Fluorophenyl)tocopherols as Novel Dioxin Receptor Antagonists
Elisabeth Kloser, Stefan Böhmdorfer, Lothar Brecker, Hanspeter Kählig, Thomas Netscher, Kurt Mereiter and Thomas Rosenau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     3-¦Â-O-[¦Â-D-2-tetracosylxylopyranosyl]-stigmasterol
    ÏàËÆ¶È:58.8%
Phytochemistry          1990          29          2957-2959
Steroid glycosides from Asparagus adscendens
Mamta Tandon,Yogendra N. Shukla,Raghunath S. Thakur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

51 .     stigmasterol-3-¦Â-O-D-gluco-pyranoside
    ÏàËÆ¶È:58.8%
Pharmazie          2002          57          206-208
Two new chlorinated amides from Nicotiana glauca R. Graham
E.Y. Backheet - H. M. Sayed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

52 .     compound 18c
[C19H34O4     ÏàËÆ¶È:58.8%
Tetrahedron          2012          68          106-113
Structure¨Cactivity relationship of novel juvenile hormone, JHSB3, isolated from the stink bug, Plautia stali
Kanako Kaihara, Toyomi Kotaki, Hideharu Numata, Yasufumi Ohfune, Tetsuro Shinada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

53 .     4-((3R,7R,11R)-3-benzoxy-3,7,11,15-tetramethylhexadec-1-ynyl)-1,6-dimethyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-5-ylformate
C37H54N2O3     ÏàËÆ¶È:58.8%
Bioorganic & Medicinal Chemistry          2010          18          7628-7638
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11.13,11.18,13.07,18.95,19.15,19.18,20.73,21.99,22.04,22.07,23.54,24.19,24.59,27.77,31.46,32.47,32.60,37.08,37.14,37.22,37.31,39.19,39.68,64.98,74.85,111.88,117.74,121.60,124.79,128.72,131.06,144.72,147.77.
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