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1 .     ¦Á-tocospiro B
    ÏàËÆ¶È:96.5%
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
2 .     VE-FPL
C29H50O4     ÏàËÆ¶È:93.1%
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
3 .     compound 23
    ÏàËÆ¶È:93.1%
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
4 .     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:89.6%
Chinese Traditional and Herbal Drugs          2010          41          370-373
½ðÁ«»¨µÄ»¯Ñ§³É·ÖÑо¿
ÁõÕÙÑô;ÂÞ¶¼Ç¿
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (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:75.8%
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
6 .     (-)-¦Á-tocospirone
C29H50O4     ÏàËÆ¶È:72.4%
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
7 .     (-)-¦Á-tocospirone
C2H50O4     ÏàËÆ¶È:72.4%
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
8 .     5-Cholesten-3¦Â-yl formate (3¦Â-cholesterylformate
C28H46O2     ÏàËÆ¶È:62.0%
Steroids          2006          71          632-638
A simple, convenient and chemoselective formylation of sterols by Vilsmeier reagent
Vandana Srivastava, Arvind Singh Negi, J.K. Kumar, M.M. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3b(2-hydroxy)-ethoxycholest-5-ene
    ÏàËÆ¶È:62.0%
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
10 .     phytyl palmitate
    ÏàËÆ¶È:62.0%
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
11 .     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:62.0%
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
12 .     4a,8a-dibromo-2,6-dimethyl-2-(4,8,12-trimethyltridecyl)-3,4,4a,8a-tetrahydro-2H-chromene-5,8-dione
C27H44Br2O3     ÏàËÆ¶È:62.0%
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
13 .     compound 32
    ÏàËÆ¶È:62.0%
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
14 .     2,2-dimethyl-3-[(3R,7R)-3,7,11-trimethyldodecyl]oxirane
    ÏàËÆ¶È:62.0%
European Journal of Organic Chemistry          2010                   2218-2225
A Straightforward Hetero-Diels¨CAlder Approach to (2-ambo,4¡äR,8¡äR)-¦Á/¦Â/¦Ã/¦Ä-4-Thiatocopherol
Stefano Menichetti, Riccardo Amorati, Maria Grazia Bartolozzi, Gian Franco Pedulli, Antonella Salvini and Caterina Viglianisi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Cholest-5-en-3¦Â-yl acetate
C29H48O2     ÏàËÆ¶È:62.0%
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
16 .     trans-phytyl palmitate
C16H31O     ÏàËÆ¶È:61.2%
Journal of Natural Products          1991          Vol 54          1444
Diterpene Fatty Acid Ester from Leucas nutans
Mashooda Hasan, Dadu Khan Burdi, Viqar Uddin Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     1,6-dimethyl-4-((3R,7R,11R)-3-hydroxy-3,7,11,15-tetramethylhexadecyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-5-ylacetate
C31H54N2O3     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
4Â¥2013-03-11 22:38:26
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