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¶ÎÇàyu(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10, ok 2015-04-17 18:30:30
1 .     (3R,6R,7E)-3-hydroxy-4,7-megastigmadien-9-one
C13H20O2     ÏàËÆ¶È:92.3%
Phytochemistry          2004          65          497-505
Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui
Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     (3R,6R ) -3- hydroxyl -¦Á- ionone
    ÏàËÆ¶È:92.3%
Chinese Chemical Letters          2003          14          62-68
Two New Ionone Derivatives from Rhododendron przewalskii Maxim.
Guo Qiang LI, Zhong Jian JIA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     (3R,6R,7E)-3-Hydroxy-4,7-megastigmadien-9-one
    ÏàËÆ¶È:92.3%
Phytochemistry          1996          41          1333-1336
Norisoprenoids from Viburnum dilatatum
Koichi Machida, Masao Kikuchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     (3R,6R)-3-hy drox yl-¦Á-ionone
    ÏàËÆ¶È:92.3%
Chemical Research in Chinese Universities          2002          18          422-424
Two New Compounds from Rhododendron Przewalskii Maxim
LI Guo-qiang, JIA Zhong-jian and ZHANG Shu-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     (3R,6R,7E)-4-hydroxy-4,7-megastigmadien-9-one
    ÏàËÆ¶È:92.3%
Chinese Traditional and Herbal Drugs          2015          46          28¨C32
Chemical constituents from Pothos chinensis
JI Ming-chang, XIAO Shi-ji, JIANG Shun-yuan, GUO Da-le, ZHOU Yan, DING Li-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     (3R,6R,7E)-3-hydroxy-4,7-megastigmadien-9-one
    ÏàËÆ¶È:92.3%
China Journal of Chinese Materia Medica          2011          36          2212-2214
Isoprenoids and Phenylpropanoids from Saussurea deltoidea
HUANG, Huoqiang, YAN, Meina, PIAO, Xianglan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     3-hydroxy-¦Á-ionone
    ÏàËÆ¶È:92.3%
Applied Microbiology and Biotechnology          2010          88          485-495
Regioselective hydroxylation of norisoprenoids by CYP109D1 from Sorangium cellulosum So ce56
Yogan Khatri, Marco Girhard, Anna Romankiewicz, Michael Ringle, Frank Hannemann, Vlada B. Urlacher, Michael C. Hutter, Rita Bernhardt
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     (3R,6R,7E)-3-hydroxy-4,7-megastigmadien-9-one
    ÏàËÆ¶È:92.3%
China Journal of Chinese Materia Medica          2014          39          1620-1624
Monoterpenes and sesquiterpenes from Clausena excavata
Peng Wenwen, Song Weiwu, Huang Maobo, Tan Ninghua
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     (3R,6R)-¦Á-ionone-3-ol
    ÏàËÆ¶È:92.3%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          133-137
Irisone Derivative from Aucklandiae Radix
XU Nan, ZHAN Hong-li, ZHONG Xu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     (3R,6R,7E)-3-hydroxy-4,7-megastigmadien-9-one
C13H20O2     ÏàËÆ¶È:84.6%
Chinese Traditional and Herbal Drugs          2014          45          1980-1983
Chemical constituents from aerial parts of Ligusticum sinense cv. chaxiong
WEI Qian, YANG Jian-bo, WANG Ai-guo, JI Teng-fei, SU Ya-lun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-04-12 11:44:56
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