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13CNMR :   52.7, 56.0, 56.1, 63.9, 89.5, 108.7, 112.2, 114.5, 119.6, 120.9, 128.7, 131.5, 132.0, 145.1, 146.1, 146.8, 190.5

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13CNMR :  13.3, 18.6, 22.6, 24.0, 26.3, 28.8, 29.0, 35.7, 41.5, 44.2, 36.6, 50.9, 52.1, 57.6, 71.3, 79.1, 79.3, 81.5, 168.8, 208.6, 213.9
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1 .     (7R,8S)-ficusal
     ÏàËÆ¶È:94.4%
Chinese Pharmaceutical Journal          2010          45          650-653
Study on Lignans from Catunaregam spinosa
GAO Guang-chun, TAO Shu-hong, ZHANG Si, LI Qing-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Curcasinlignan B
C18H18O6     ÏàËÆ¶È:94.4%
Zeitschrift f¨¹r Naturforschung B          2012          67          176-180
New Lignans from Jatropha curcas Linn.
J. J. Xu and N. H. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Ficusal
     ÏàËÆ¶È:77.7%
Journal of Chinese Pharmaceutical Sciences          2010          19          95-99
Chemical ingredients isolated from the aerial parts of Artemisia anomala
Ke Zan; Xiao-Qing Chen; Qiang Fu; Si-Xiang Zhou; Mei-Tian Xiao; Jing Wen; Peng-Fei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     threo-2,3-Bis-(4-hydroxy-3-methoxyphenyl)-3-raethoxy-propanol
C18H22O6     ÏàËÆ¶È:76.4%
Phytochemistry          1995          39          899-902
Lignans from the wood of Aralia bipinnata
Jeh-Jian Hsiao, Hung-Cheh Chiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (-)-balanophonin
C20H20O6     ÏàËÆ¶È:73.6%
Korean Journal of Pharmacognosy          2001          32(4)          302-306
Chemical Components from the Stem Barks of Kalopanax septemlobus
Hong, Sung-Su; Han, Doo-Il; Hwang, Bang-Yeon; Choi, Woo-Hoi; Kang, Ho-Sang; Lee, Myung-Koo; Lee, Don-Koo; Lee, Kyong-Soon; Ro, Jai-Seup
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (2R,3R )-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-methylbenzofuran-5-carboxylic acid
     ÏàËÆ¶È:72.2%
Phytochemistry          1999          52          345-350
2,3-Dihydrobenzofuran neolignans from Aristolochia pubescens
Isabele R. Nascimento, Lucia M.X. Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Curcasinlignan C
C18H18O5     ÏàËÆ¶È:72.2%
Zeitschrift f¨¹r Naturforschung B          2012          67          176-180
New Lignans from Jatropha curcas Linn.
J. J. Xu and N. H. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     perseal F
C18H18O5     ÏàËÆ¶È:70.5%
Planta Medica          2001          67          559-561
Cytotoxic Neolignans and Butanolides from Machilus obovatifolia
Ian-Lih Tsai, Jyh-Huey Chen, Chang-Yih Duh,Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Compound 1
     ÏàËÆ¶È:70.5%
Bioorganic & Medicinal Chemistry          2008          16          2645-2650
Low molecular weight lignin suppresses activation of NF-¦ÊB and HIV-1 promoter
Shinya Mitsuhashi, Takao Kishimoto, Yasumitsu Uraki, Takashi Okamoto, Makoto Ubukata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     balanophonin
     ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          1982          30          1525-1527
BALANOPHONIN, A NEW NEO-LIGNAN FROM BALANOPHORA JAPONICA MAKINO
Mitsumasa Haruna,Tomoko Koube,Kazuo Ito and Hiroyuki Murata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     melianoninol
C20H20O6     ÏàËÆ¶È:70%
Journal of Chinese Pharmaceutical Sciences          1992          1          7-11
Studies on the Chemical Constituents of Melia azedarach
Ren-Sheng Xu; Wen-Han Lin; Jiu Han; Wen-Lu Wang; Shan-Huan Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     melianoninol
C20H20O6     ÏàËÆ¶È:70%
Acta Pharmaceutica Sinica          1991          26          426-429
STUDIES ON THE CHEMICAL CONSTITUENTS OF MELIA AZEDARACH L.
J Han; WH Lin; RS Xu; WL Wang and SH Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     balanophonin
C20H20O6     ÏàËÆ¶È:70%
Phytochemistry          1999          50          781-785
Coniferaldehyde derivatives from tissue culture of Artemisia annua and Tanacetum parthenium
Lai-King Sy, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 6
     ÏàËÆ¶È:70%
Chinese Pharmaceutical Journal          2002          37          14-17
Study on chemical constituents isolated from Glycosmis citrifolia
SHEN Xiao-Ling, ZENG Hui-Fang, CHEN Zhen, ZHONG Guang-Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (E)-3-[(2S,3R)-2,3-dihydro-2-(4'-hydroxy-3'-methoxyphenyl)-3-hydroxymethyl-7-methoxy-1-benzofuran-5-yl]-2-propenal
C20H20O6     ÏàËÆ¶È:70%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (E)-3-[(2R,3S)-2,3-dihydro-2-(4'-hydroxy-3'-methoxyphenyl)-3-hydroxyemthyl-7-methoxy-1-benzofuran-5-yl]-2-propenal
C20H20O6     ÏàËÆ¶È:70%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     Curcasinlignan A
C20H20O6     ÏàËÆ¶È:70%
Zeitschrift f¨¹r Naturforschung B          2012          67          176-180
New Lignans from Jatropha curcas Linn.
J. J. Xu and N. H. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Balanophonin
C20H20O6     ÏàËÆ¶È:70%
Plant Diversity and Resources          2013          35          209-215
Antioxidant Constituents from Pinus massoniana (Pinaceae)
ZHANG Yu-Mei, GONG Qing-Fang, YANG Jia-Qian, ZENG Guang-Zhi, TAN Ning-Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     threo-2,3-bis(4-hydroxy-3-methoxyphenyl)-3-ethoxypropan-1-ol
C16H16O4     ÏàËÆ¶È:68.4%
Journal of Natural Products          2002          65          1497-1500
Five New Phenolics from the Roots of Ficus beecheyana
Tzong-Huei Lee,Yuh-Chi Kuo,Guei-Jane Wang,Yueh-Hsiung Kuo,Chi-I Chang, Chung-Kung Lu, and Ching-Kuo Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (9S*,10S*)-3-[7-(3,10-dihydroxy-9-hydroxymethyl-2,5-dimethoxy)-9,10-dihydrophenanthrenyl]propenal
C20H20O6     ÏàËÆ¶È:68.4%
Journal of Natural Products          2001          64          832-835
New Dihydrophenanthrene and Phenyldihydroisocoumarin Constituents of Trema orientalis
M.-Genevi¨¨ve Dijoux-Franca,Diderot Noungou¨¦ Tchamo, Bruno Cherel, Max Cussac, Etienne Tsamo, and Anne-M. Mariotte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     Balanophonin
     ÏàËÆ¶È:68.4%
Molecules          2010          15          4011-4016
Aquilarin A, a New Benzenoid Derivative from the Fresh Stem of Aquilaria sinensis
Qing-Huang Wang, Ke Peng, Le-He Tan and Hao-Fu Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     9,10-threo-3-[7-(3,10-dihydroxy-9-hydroxymethyl-2,5-dimethoxy)-9,10-dihydrophenanthrenyl]propenal
C20H20O6     ÏàËÆ¶È:68.4%
Journal of Chemistry          2009          47          716-719
Isoflavones and dihydrophenanthrene from Dalbergia tonkinensis.
Trần Anh Tuấn, Nguyễn Tiến Đạt, Nguyễn Ho¨¤i Nam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     (E)-3-[(2S,3R)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(4'-hydroxy-3'-methoxyphenyl)-1-benzofuran-5-yl]-2-propen-1-ol
     ÏàËÆ¶È:68.4%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (E)-3-[(2R,3S)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(4'-hydroxy-3'-methoxyphenyl)-1-benzofuran-5-yl]-2-propen-1-ol
     ÏàËÆ¶È:68.4%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     balanophonin
     ÏàËÆ¶È:68.4%
Chinese Journal of Natural Medicines          2011          9          112-114
Chemical Constituents from Dragon's Blood of Dracaena cambodiana
LUO Ying,, DAI Hao-Fu, WANG Hui, MEI Wen-Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     xylobuxin
C21H22O7     ÏàËÆ¶È:66.6%
Journal of Natural Products          1995          Vol 58          786-789
Isolation and Structure Elucidation of Xylobuxin, a New Neolignan from Xylopia buxifolia
Anne Wahl, François Roblot, Andr¨¦ Cav¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-02 10:46:05
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

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¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï
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²éѯ½á¹û£º¹²²éµ½386¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
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1 .     (3R,4R,5S)-ethyl 4-acetamido-5-[(tert-butoxycarbonyl)amino]-3-(pentan-3-yloxy)-2-[2-(triethoxysilyl)ethyl]cyclohex-1-enecarboxylate
C29H54N2O9Si     ÏàËÆ¶È:66.6%
Heterocycles          2012          86          1565-1574
SYNTHESIS OF A NEW OSELTAMIVIR DERIVATIVE THROUGH LATE-STAGE CATALYTIC C¨CH FUNCTIONALIZATION
Kenta Saito and Motomu Kanai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     scabrolide C
C20H26O6     ÏàËÆ¶È:61.9%
Journal of Natural Products          2002          65          1904-1908
Scabrolides A-D, Four New Norditerpenoids Isolated from the Soft Coral Sinularia scabra
Jyh-Horng Sheu,Atallah F. Ahmed, Ru-Ting Shiue, Chang-Feng Dai, and Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ring B-homo derivative
     ÏàËÆ¶È:61.9%
Natural Product Research          1993          1          257-262
Rearrangements of Derivatives of Methyl 9,11-Dihydroxy-(-)-Kauran-19-Oate to New Skeletal Diterpenes
Tatsuhiko Nakano; Maria Aracelis Maillo; Alfredo Usubillaga; Andrew T. McPhail; Donald R. McPhail
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     17¦Á-hydroxy-3¦Á,21-disulfooxy-5¦Â-pregnane-11,20-dione disodium salt
C21H30O11SNa2     ÏàËÆ¶È:61.9%
Chemical & Pharmaceutical Bulletin          2010          58          344-353
Potential Corticoid Metabolites: Chemical Synthesis of 3- and 21-Monosulfates and Their Double-Conjugates of Tetrahydrocorticosteroids in the 5¦Á- and 5¦Â-Series
Rika Okihara, Kuniko Mitamura, Maki Hasegawa, Megumi Mori, Akina Muto, Genta Kakiyama, Shoujiro Ogawa, Takashi Iida, Miki Shimada, Nariyasu Mano and Shigeo Ikegawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (2¦Á,3¦Á,5¦Á,20R)-2,3-epoxypregnan-20-ol
C21H34O2     ÏàËÆ¶È:61.9%
Steroids          2012          77          1403-1418
Solid-phase chemical synthesis and in vitro biological evaluation of novel 2¦Â-piperazino-(20R)-5¦Á-pregnane-3¦Á,20-diol N-derivatives as anti-leukemic agents
Hajer Jegham, Ren¨¦ Maltais, Philippe Dufour, Jenny Roy, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     compound 6a
C18H30O4     ÏàËÆ¶È:61.9%
Asian Journal of Organic Chemistry          2013          2          593-599
Total Synthesis of Both Spiroketal Diastereomers of the Reported Structure of Cephalosporolide H
Prof. Rodney A. Fernandes and Mahesh B. Halle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 6b
C18H30O4     ÏàËÆ¶È:61.9%
Asian Journal of Organic Chemistry          2013          2          593-599
Total Synthesis of Both Spiroketal Diastereomers of the Reported Structure of Cephalosporolide H
Prof. Rodney A. Fernandes and Mahesh B. Halle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Methyl 6¦Á,7¦Á-dihydroxy-ent-atis-16-en-19-oate
C21H32O4     ÏàËÆ¶È:61.9%
Natural Product Communications          2008          3          483-494
Ring Contraction of Gummiferolic Acid, a DiterpeneIsolated from Margotia gummifera, Leading toAtisagibberellins
Josefa Anaya, Juan Jos¨¦ Fern¨¢ndez, Manuel Grande, , Justo Marti¨¢ñez and Pascual Torres
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     eriocalyxin C
C22H28O7     ÏàËÆ¶È:59.0%
Journal of Natural Products          1999          62          782-784
Diterpenoids from Isodon eriocalyx
Shao-Nong Chen, Jian-Min Yue, Shao-Yuan Chen, Zhong-Wen Lin, Guo-Wei Qin, Han-Dong Sun, and Yao-Zu Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     eriocalyxin C
C22H28O7     ÏàËÆ¶È:59.0%
Chinese Chemical Letters          1998          9          1025-1028
Three New Diterpenoids from Isodon Eriocalyx
shao Nong CHEN,Shao Yuan CHEN,Jian Min YUE,Zhong Wen LIN,Guo Wei QIN,Han Dong SUN,and Yao Zu CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     gymnandine
C22H33NO     ÏàËÆ¶È:59.0%
Acta Pharmaceutica Sinica          1993          28          188-191
DITERPENOID ALKALOIDS FROM ACONITUM GYMNANDRUM
LS Ding; FE Wu and YZ Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 2
     ÏàËÆ¶È:59.0%
Phytochemistry          1989          28          543-551
Diterpenes and other constituents from Australian Helichrysum and related species
J. Jakupovic,A. Schuster,F. Bohlmann,U. Ganzer,R.M. King,H. Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 19b
C24H36O9     ÏàËÆ¶È:58.3%
Heterocycles          2000          53          599-612
Hydrogenation Derivatives of Neo-clerodanes and Their Antifeedant Activity
Maurizio Bruno, Sergio Rosselli, Ivana Pibiri, Franco Piozzi,* and Monique S. J. Simmonds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 19b
C24H36O9     ÏàËÆ¶È:58.3%
Heterocycles          2000          53          599-612
Hydrogenation Derivatives of Neo-clerodanes and Their Antifeedant Activity
Maurizio Bruno, Sergio Rosselli, Ivana Pibiri, Franco Piozzi,* and Monique S. J. Simmonds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (13S,14R)-ent-3¦Â-hydroxy-12-oxo-8¦Á,13;14,15-diepoxylabdane
C20H32O4     ÏàËÆ¶È:57.1%
Phytochemistry          2004          65          107-115
Biotransformation of ent-13-epi-manoyl oxides difunctionalized at C-3 and C-12 by filamentous fungi
Andr¨¦s Garc¨ªa-Granados, Antonia Fern¨¢ndez, Mar¨ªa C. Guti¨¦rrez,Antonio Mart¨ªnez, Raquel Quir¨®s, Francisco Rivas, Jos¨¦M. Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Pregnenolone
C21H32O2     ÏàËÆ¶È:57.1%
Acta Botanica Yunnanica          1997          19(1)          92-96
STUDY ON CHEMICAL CONSTITUENTS OF SAUSSUREA LAPPA ¢ò
Yang Hui, ¡¡Xie J inlun,¡¡Sun Handong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     pregnenolone
     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          1984          20          177-182
CATALYTIC REARRANGEMENT OF ¦Á-D-GLUCOSE 1,2-ORTHOACETATE DERIVATIVES OF PREGNENOLONE AND 16-DEHYDROPREGNENOLONE
N. F. Samoshina, V. A. Denisenko, V. L. Novikov, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     De-A,B-24-oxo-23,25-(isopropylidenedioxy)-cholestan-8-ol
C20H33O4     ÏàËÆ¶È:57.1%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     De-A,B-24-oxo-23,25-(isopropylidenedioxy)-cholestan-8-one
C21H35O4     ÏàËÆ¶È:57.1%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     compound 11
     ÏàËÆ¶È:57.1%
Steroids          2002          67          621-626
13C-NMR study of 4-azasteroids in solution and solid state
Jacek W. Morzycki, Iwona Wawer, Agnieszka Gryszkiewicz, Jadwiga Maj, Leszek Siergiejczyk, Alicja Zaworska
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     3¦Â-Hydroxy[19-2H3]pregn-5-en-20-one
C21H29H3O2     ÏàËÆ¶È:57.1%
Steroids          2004          69          161-171
Synthesis of [19-2H3]-analogs of dehydroepiandrosterone and pregnenolone and their sulfates
Ivan Černý, Vladim¨ªr Pouzar, Miloš Budĕš¨ªnský, Marie Biĕ¨ªkov¨¢, Martin Hill, Richard Hampl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     3¦Â-Hydroxy[19-2H2]pregn-5-en-20-one
     ÏàËÆ¶È:57.1%
Steroids          2004          69          161-171
Synthesis of [19-2H3]-analogs of dehydroepiandrosterone and pregnenolone and their sulfates
Ivan Černý, Vladim¨ªr Pouzar, Miloš Budĕš¨ªnský, Marie Biĕ¨ªkov¨¢, Martin Hill, Richard Hampl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     compound
     ÏàËÆ¶È:57.1%
Steroids          2004          69          161-171
Synthesis of [19-2H3]-analogs of dehydroepiandrosterone and pregnenolone and their sulfates
Ivan Černý, Vladim¨ªr Pouzar, Miloš Budĕš¨ªnský, Marie Biĕ¨ªkov¨¢, Martin Hill, Richard Hampl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (13S,14S)-14-Hydroxy-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstan-17-one 17-oxime
     ÏàËÆ¶È:57.1%
Steroids          2004          69          511-514
Reaction of (13S)-13-iodo-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstane-14,17-dione with hydroxylamine and its application to the synthesis of new 13,14-seco steroids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Galina P. Fando, Yuliya Y. Zhiburtovich, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     pregnenolone
C21H32O2     ÏàËÆ¶È:57.1%
Journal of Asian Natural Products Research          2002          4          33-41
CONSTITUENTS FROM THE ROOTS OF HERACLEUM RAPULA FRANCH
XUE-MEI NIU, SHENG-HONG LI, BEI JIANG, QIN-SHI ZHAO and HAN-DONG SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     pergnenolone
     ÏàËÆ¶È:57.1%
Natural Product Research          2006          20          860-865
A new dihydroisocoumarin from the rhizomes of Notopterygium forbesii
Yan-Hui Li; Fan Luo; Shu-Lin Peng; Jian Liang; Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     torilolone 11-O-¦Â-D-glucopyranoside
C21H34O8     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1998          46          1743-1747
New Guaiane-Type Sesquiterpenoid Glycosides from Torillis japonica Fruit
Junichi KITAJIMA,Nobuyuki SUZUKI and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     7¦Â,8¦Â-dihydroxystemodin
C20H34O4     ÏàËÆ¶È:57.1%
Journal of Natural Products          1991          Vol 54          1543
Preparation, Characterization, and Antiviral Activity of Microbial Metabolites of Stemodin
Charles D. Hufford, Farid A. Badria, Mohamed Abou-Karam, W. Thomas Shier, Robin D. Rogers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     methyl(13R,14S)-ent-3¦Â,16-dihydroxy-8¦Á,13;14,15-diepoxylabdan-18-oate
     ÏàËÆ¶È:57.1%
Phytochemistry          1995          38          287-293
Synthesis of enantio-manoyl oxides: Modifiers of the activity of adenylatecyclase enzyme
Andr¨¦s Garc¨ªa-Granados, Emilio Liñ¨¢n, Antonio Mart¨ªnez, M.Esther Onorato, Andr¨¦s Parra, Jos¨¦Mar¨ªa Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     chaparramarin
C20H28O6     ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          3262-3264
Structure of chaparramarin, a quassinoid from Castela tortuosa
Isao Kubo, Yoshihiro Murai, Swapan K. Chaudhuri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     11¦Â,17¦Á-dihydroxy-3¦Á,21-disulfooxy-5¦Â-pregnan-20-one disodium salt
C21H32O11S2Na2     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2010          58          344-353
Potential Corticoid Metabolites: Chemical Synthesis of 3- and 21-Monosulfates and Their Double-Conjugates of Tetrahydrocorticosteroids in the 5¦Á- and 5¦Â-Series
Rika Okihara, Kuniko Mitamura, Maki Hasegawa, Megumi Mori, Akina Muto, Genta Kakiyama, Shoujiro Ogawa, Takashi Iida, Miki Shimada, Nariyasu Mano and Shigeo Ikegawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     (1R,3aR,4S,7aR)-1-((S)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-1H-inden-4-ol
C18H34O2     ÏàËÆ¶È:57.1%
Heterocycles          2010          81          381-394
Synthesis of 20-Epi-eldecalcitol [20-Epi-1¦Á,25-dihydroxy-2¦Â-(3-hydroxypropoxy)vitamin D3: 20-Epi-ED-71]
Madoka Yoshino, Kohei Eto, Keisuke Takahashi, Jun Ishihara, Susumi Hatakeyama, Yoshiyuki Ono, Hitoshi Saito, and Noboru Kubodera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     (1R,3aR,4S,7aR)-1-((S)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-1H-inden-4(2H)-one
C18H32O2     ÏàËÆ¶È:57.1%
Heterocycles          2010          81          381-394
Synthesis of 20-Epi-eldecalcitol [20-Epi-1¦Á,25-dihydroxy-2¦Â-(3-hydroxypropoxy)vitamin D3: 20-Epi-ED-71]
Madoka Yoshino, Kohei Eto, Keisuke Takahashi, Jun Ishihara, Susumi Hatakeyama, Yoshiyuki Ono, Hitoshi Saito, and Noboru Kubodera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     Pregnenolone
     ÏàËÆ¶È:57.1%
Steroids          1995          60          442-446
Complete 1H and 13C NMR spectra of pregnenolone
Zsuzsa Szendi, Peter Forg¨®, Frederick Sweet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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