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1 .     (-)-¦Á-tocospirone
C29H50O4     ÏàËÆ¶È:93.1%
Planta Medica          2003          69          757-764
Anti-Platelet Aggregation and Chemical Constituents from the Rhizome of Gynura japonica
Wei-Yu Lin,Yueh-Hsiung Kuo,Ya-Ling Chang, Che-Ming Teng,Eng-Chi Wang, Tsutomu Ishikawa,Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (2R,4aR,8aR)-3,4,4a,8a-tetrahydro-4a-hydroxy-2,6,7,8a-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-chromene-5,8-dione
C29H50O4     ÏàËÆ¶È:93.1%
Helvetica Chimica Acta          2009          92          2762-2768
Three Terpenoids and a Tocopherol-Related Compound from Ricinus communis
Qin-Gang Tan, Xiang-Hai Cai, Zhi-Zhi Du, Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (-)-¦Á-tocospirone
C2H50O4     ÏàËÆ¶È:93.1%
Acta Bot. Boreal. -Occident. Sin.          2007          27          0532-0536
Chemical Component froMallelopathic Cultivar Sunflower Leaves
GAO Yuan, YANG Wan-qiu, WANG Fei, LIU Ji-kai, GAO Jin-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     VE-FPL
C29H50O4     ÏàËÆ¶È:72.4%
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

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5 .     ¦Á-tocospiro B
    ÏàËÆ¶È:72.4%
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

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6 .     ¦Á-Tocospiro A
C29H50O4     ÏàËÆ¶È:72.4%
Tetrahedron Letters          2003          44          5125-5128
Two novel ¦Á-tocopheroids from the aerial roots of Ficus microcarpa
Yi-Ming Chiang, Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     ¦Á-Tocospiro B
C29H50O4     ÏàËÆ¶È:72.4%
Tetrahedron Letters          2003          44          5125-5128
Two novel ¦Á-tocopheroids from the aerial roots of Ficus microcarpa
Yi-Ming Chiang, Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     4a-bromo-2,6,7,8a-tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4,4a,8a-tetrahydro-2H-chromene-5,8-dione
C29H49BrO3     ÏàËÆ¶È:72.4%
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

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9 .     phytyl palmitate
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2007          19          944-947
Chemical Constituents of Chondria crassicaulis
YIN Shuai-wen;SHI Yan-ping; LI Xiao-ming; WANG Bin-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     4a,8a-dibromo-2,6,7-trimethyl-2-(4,8,12-trimethyltridecyl)-3,4,4a,8a-tetrahydro-2H-chromene-5,8-dione
C28H46Br2O3     ÏàËÆ¶È:71.4%
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

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11 .     compound 23
    ÏàËÆ¶È:71.4%
Journal of Agricultural and Food Chemistry          2003          51          2949-2957
Isolation, Structural Elucidation, and Inhibitory Effects of Terpenoid and Lipid Constituents from Sunflower Pollen on Epstein−Barr Virus Early Antigen Induced by Tumor Promoter, TPA
Motohiko Ukiya, Toshihiro Akihisa, Harukuni Tokuda, Kazuo Koike, Junko Takayasu, Hiroki Okuda, Yumiko Kimura, Tamotsu Nikaido, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     ((3R,7R,11R)-3-hydroxy-3,7,11,15-tetramethylhexadecyl)-1,6-dimethyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-5-ol
C29H52N2O2     ÏàËÆ¶È:70%
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

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13 .     fucosterol
    ÏàËÆ¶È:68.9%
Chinese Journal of Natural Medicines          2010          8          326-329
Chemical Constituents from Grateloupia filicina
XU Yin-Feng; WANG Bin; SU Chuan-Ling; QU You-Le
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     cholesterol
    ÏàËÆ¶È:67.8%
Chemical & Pharmaceutical Bulletin          1979          27          38-42
Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids
NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     phytyl-1-hexanoate
    ÏàËÆ¶È:67.8%
Natural Product Research          2007          21          828-833
Lipid constituents of Trifolium resupinatum var. microcephalum
Temine Sabudak; Emel Isik; Sevil Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     cholest-5-ene-3¦Â-ol
    ÏàËÆ¶È:67.8%
China Journal of Chinese Materia Medica          2009          34          60-63
Bioactivity sterols from red alga Acanthophora spicifera boergesen
HAN Lijun, SHI Dayong, XU Feng, YUAN Zhaohui, SUN Jie, SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     3a-acetyl-2,3,5-trimethyl-7a-hydroxy-5-(4,8,12-2trimethyl-tridecanyl)-1,3a,5,6,7,7a-hexahydro-4-oxainden-1-one
    ÏàËÆ¶È:67.8%
Chinese Traditional and Herbal Drugs          2010          41          370-373
½ðÁ«»¨µÄ»¯Ñ§³É·ÖÑо¿
ÁõÕÙÑô;ÂÞ¶¼Ç¿
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     2-bromo-¦Ã-tocopherylquinone
C28H47BrO3     ÏàËÆ¶È:67.8%
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

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19 .     3¦Â-Methoxycholest-5-ene
C28H48O     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-09-23 18:30:51
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