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12.1,14.5,19.6,23.8,25.5,26.5,27.4,30.3,30.4,30.5,32.8,36.0,36.7,38.5,40.6,52.0,57.5,61.6,107.6,111.9,118.7,120.3,122.7,129.7,136.8,139.9
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×ÏËÕÒ»ÓÄÏã: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2012-06-04 15:21:55
¶¹¸ç: ½ð±Ò+1, лл²ÎÓë½»Á÷ 2012-06-04 16:08:19
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1 .     iso-hymenamide C
    ÏàËÆ¶È:69.2%
Tetrahedron          2001          57          6249-6255
Synthesis, structural aspects and bioactivity of the marine cyclopeptide hymenamide C
Assunta Napolitano, Ines Bruno, Paolo Rovero, Rut Lucas, Miguel Pay¨¤ Peris, Luigi Gomez-Paloma, Raffaele Riccio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     hermitamide B
C25H38N2O2     ÏàËÆ¶È:61.5%
Journal of Natural Products          2000          63          952-955
Hermitamides A and B, Toxic Malyngamide-Type Natural Products from the Marine Cyanobacterium Lyngbya majuscula
Lik Tong Tan, Tatsufumi Okino, and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (25S)-3¦Â -Hydroxy-5¦Â -spirostan-23-ene-23-nitramine
C27H42O5N2     ÏàËÆ¶È:61.5%
Steroids          2006          71          2010-12-17
New bisfuran derivative from sarsasapogenin: An X-ray and NMR analysis
Yliana L¨®pez, Rosa Santillan, Norberto Farf¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound D3
    ÏàËÆ¶È:61.5%
Steroids          2010          75          926-935
Chemical synthesis of 20S-hydroxyvitamin D3, which shows antiproliferative activity
Wei Li, Jianjun Chen, Zorica Janjetovic, Tae-Kang Kim, Trevor Sweatman, Yan Lu, Jordan Zjawiony, Robert C. Tuckey, Duane Miller, Andrzej Slominski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     N16-Desmethylhemiasterlin
C29H44N4O4     ÏàËÆ¶È:61.5%
Journal of Natural Products          2003          66          183-199
Synthesis and Antimitotic/Cytotoxic Activity of Hemiasterlin Analogues
James A. Nieman, John E. Coleman, Debra J. Wallace, Edward Piers, Lynette Y. Lim, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (24S)-24-Methylcholest-5,9-diene-1¦Á,3¦Â-diol
C28H46O2     ÏàËÆ¶È:60.7%
Bulletin of the Chemical Society of Japan          2008          81          1616-1620
Anti-Inflammatory Polyoxygenated Steroids from the Soft Coral Sinularia sp.
Jui-Hsin Su, Ching-Li Lo, Yi Lu, Zhi-Hong Wen, Chiung-Yao Huang, Chang-Feng Dai, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     1-[(3R,4R)-1-Cyclooctylmethyl-3-hydroxymethyl-4-piperidinyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one
    ÏàËÆ¶È:59.2%
Bioorganic & Medicinal Chemistry          2008          16          822-829
A new synthesis of the ORL-1 antagonist 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidinyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397) and activity in a calcium mobilization assay
Emilie D. Smith, N. Ariane Vinson, Desong Zhong, Bertold D. Berrang, Jennifer L. Catanzaro, James B. Thomas, Hern¨¢n A. Navarro, Brian P. Gilmour, Jeffrey Deschamps, F. Ivy Carroll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     petilidine
    ÏàËÆ¶È:59.2%
Chinese Traditional and Herbal Drugs          2009          40          15-17
Alkaloid constituents of Fritillaria cirrhosa
CAO Xin-wei; ZHANG Meng; LI Jun; XIAO Pei-gen; CHEN Si-bao; CHEN Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (S)-N¦Á,N1,¦Â,¦Â-Tetramethyltryptophanyl-(S)-tert-leucyl-(2e)-N-methyl-4-amino-2-methylbut-2-enoic acid
C27H40N4O4     ÏàËÆ¶È:57.6%
Journal of Natural Products          2003          66          183-199
Synthesis and Antimitotic/Cytotoxic Activity of Hemiasterlin Analogues
James A. Nieman, John E. Coleman, Debra J. Wallace, Edward Piers, Lynette Y. Lim, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     compound 5
C25H51ON3     ÏàËÆ¶È:57.6%
Journal of Natural Products          1997          60          495-496
Cytotoxic Acylated Spermidine from a Soft Coral, Sinularia sp.
Young-Hee Choi and Francis J. Schmitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Gordonoside A
C26H38O5     ÏàËÆ¶È:57.6%
Steroids          2007          72          559-568
Steroidal glycosides from Hoodia gordonii
Stefano Dall¡¯Acqua, Gabbriella Innocenti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 6
C28H45N3SO3     ÏàËÆ¶È:57.6%
Journal of Natural Products          1992          Vol 55          389
(-)-Agelasidine C and (-)-Agelasidine D, Two New Hypotaurocyamine Diterpenoids from the Caribbean Sea Songe Agelas clathrodes
Jos¨¦ J. Morales, Abimael D. Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     friedolabd-5-en-15,18-dioic acid
C22H36O4     ÏàËÆ¶È:57.6%
Phytochemistry          1991          30          3669-3677
Friedolabdanes and other constituents from chileanHaplopappus species
C. Zdero, F. Bohlmann, H.M. Niemeyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     12-O-¦Â-tigloyl-3¦Â,14¦Â-dihydroxy-pregn-5-ene-20-one(Hoodigonenin A)
C26H38O5     ÏàËÆ¶È:57.6%
Steroids          2011          76          702-708
Synthesis of Hoodigogenin A, aglycone of natural appetite suppressant glycosteroids extracted from Hoodia gordonii
Philippe Geoffroy, Blandine Ressault, Eric Marchioni, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     cis-N,N-Dimethyl-2-(2-heptyloxyphenylcarbamoyloxy)cyclohepthylmethylammonium Chloride
C24H41N2O3Cl     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          2011          59(8)          978-983
Synthesis and Characterization of Two Homologous Series of Diastereomeric 2-Alkoxyphenylcarbamates
Fridrich GREGAN, Juraj GREGAN, and Marek SKORSEPA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     cis-N,N-Dimethyl-2-(2-octyloxyphenylcarbamoyloxy)cyclohepthylmethylammonium Chloride
C25H43N2O3Cl     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          2011          59(8)          978-983
Synthesis and Characterization of Two Homologous Series of Diastereomeric 2-Alkoxyphenylcarbamates
Fridrich GREGAN, Juraj GREGAN, and Marek SKORSEPA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (24S)-24-methylcholeserol
C28H48O     ÏàËÆ¶È:57.6%
Chinese Journal of Marine Drugs          1998          1          17-20
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE HARD CORAL ACROPORA PULCHRA FROM THE SOUTH CHINA SEA
Xiao Ding jun, Deng Songzhi, Li Fengying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 6
    ÏàËÆ¶È:57.6%
Phytochemistry          1987          26          3037-3040
Labdane diterpenoids from Halimium viscosum and H. verticilatum
Julio G. Urones,Isidro S¨¢nchez Marcos,David Diez Martin,F.M.S.Brito Palma,Jes¨²s M. Rodilla
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 10
    ÏàËÆ¶È:57.6%
Phytochemistry          1988          27          1173-1179
Pregnane glycosides from an antitumour fraction of Periploca sepium
Hideji itokawa,Junping Xu,Koichi Takeya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     compound 6
    ÏàËÆ¶È:57.6%
Phytochemistry          1986          25          711-713
Labdane diterpenoids from Halimium viscosum
Joaqu¨ªn De Pascual Teresa, Julio G. Urones, Isidro S. Marcos, David D¨ªez Mart¨ªn, Victoria M. Alvarez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     N-(2-(1H-indol-3-yl)ethyl)hexadecanamide
C26H42N2O     ÏàËÆ¶È:57.6%
Bioorganic & Medicinal Chemistry          2010          18          5103-5113
Tryptamine-derived alkaloids from Annonaceae exerting neurotrophin-like properties on primary dopaminergic neurons
Fanny Schmidt, Gael Le Douaron, Pierre Champy, Majid Amar, Blandine S¨¦on-M¨¦niel, Rita Raisman-Vozari, Bruno Figad¨¨re
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     N-(2-(1H-indol-3-yl)ethyl)-octadeca-9Z,12Z-dienamide
C28H42N2O     ÏàËÆ¶È:57.6%
Bioorganic & Medicinal Chemistry          2010          18          5103-5113
Tryptamine-derived alkaloids from Annonaceae exerting neurotrophin-like properties on primary dopaminergic neurons
Fanny Schmidt, Gael Le Douaron, Pierre Champy, Majid Amar, Blandine S¨¦on-M¨¦niel, Rita Raisman-Vozari, Bruno Figad¨¨re
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     (5'R,20S)-20-(3-isopropyl-4,5-dihydroisoxazol-5-yl)pregn-5-en-3¦Â-ol
    ÏàËÆ¶È:57.6%
Russian Journal of Organic Chemistry          2002          38          355-360
Modification of A and B Rings in 20-Dihydroisoxazolyl Steroids and Their Derivatives with a Functionalized Side Chain
R. P. Litvinovskaya, N. V. Koval' and V. A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (22R,22S)-cholest-5-ene-3¦Â,22,24-triol
    ÏàËÆ¶È:57.6%
Russian Journal of Organic Chemistry          2002          38          355-360
Modification of A and B Rings in 20-Dihydroisoxazolyl Steroids and Their Derivatives with a Functionalized Side Chain
R. P. Litvinovskaya, N. V. Koval' and V. A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     5,14-Dimethylbudmunchiamine L1
C32H66N4O     ÏàËÆ¶È:57.6%
Natural Product Communications          2009          4          791-796
Antimicrobial, Antiparasitic and Cytotoxic SpermineAlkaloids from Albizia schimperiana
Volodymyr Samoylenko, Melissa R. Jacob, Shabana I. Khan, Jianping Zhao,Babu L. Tekwani, Jacob O. Midiwo, Larry A. Walker and Ilias Muhammad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     2-(1H-indol-3-yl)-ethyl (7S,4E)-methoxytetradecenamide
C25H38N2O2     ÏàËÆ¶È:57.6%
Bioorganic & Medicinal Chemistry          2011          19          4322-4329
Synthesis and evaluation of hermitamides A and B as human voltage-gated sodium channel blockers
Eliseu O. De Oliveira, Kristin M. Graf, Manoj K. Patel, Aparna Baheti, Hye-Sik Kong, Linda H. MacArthur, Sivanesan Dakshanamurthy, Kan Wang, Milton L. Brown, Mikell Paige
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     2-(1H-indol-3-yl)-ethyl (7R,4E)-methoxytetradecenamide
C25H38N2O2     ÏàËÆ¶È:57.6%
Bioorganic & Medicinal Chemistry          2011          19          4322-4329
Synthesis and evaluation of hermitamides A and B as human voltage-gated sodium channel blockers
Eliseu O. De Oliveira, Kristin M. Graf, Manoj K. Patel, Aparna Baheti, Hye-Sik Kong, Linda H. MacArthur, Sivanesan Dakshanamurthy, Kan Wang, Milton L. Brown, Mikell Paige
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     isophysalin B
C28H30O9     ÏàËÆ¶È:57.1%
Phytochemistry          1993          34          529-533
Physalin and neophysalins from Physalis alkekengi var. francheti and their differentiation inducing activity
Reiko Sunayama, Masanori Kuroyanagi, Kaoru Umehara, Akira Ueno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     (23E)-25-Methoxy-cholesta-5,23-dien-3¦Â-ol
C28H46O2     ÏàËÆ¶È:57.1%
Marine drugs          2011          9          162-183
New Cytotoxic Oxygenated Sterols from the Marine Bryozoan Cryptosula pallasiana
Xiang-Rong Tian,Hai-Feng Tang,Yu-Shan Li,Hou-Wen Lin,Xiao-Li Chen,Ning Ma,Min-Na Yao and Ping-Hu Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     compound 4b(minor isomer)
    ÏàËÆ¶È:57.1%
Heterocycles          2007          73          729-742
Lithium Bromide-Promoted Three-Component Synthesis of Oxa-Bridged Tetracyclic Tetrahydroisoquinolines
Aude Fayol, Eduardo Gonz¨¢lez-Zamora, Mich¨¨le Bois-Choussy, and Jieping Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     Asporyzin C
C28H39NO2     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry Letters          2010          20          5677-5680
Indoloditerpenes from an algicolous isolate of Aspergillus oryzae
Ming-Feng Qiao, Nai-Yun Ji, Xiang-Hong Liu, Ke Li, Qing-Mei Zhu, Qin-Zhao Xue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     terpendole E
C28H39NO3     ÏàËÆ¶È:57.1%
The Journal of Antibiotics          1995          48          793-804
Terpendoles, Novel AC AT Inhibitors Produced by Albophoma yamanashiensis III. Production, Isolation and Structure Elucidation of New Components
HIROSHI TOMODA, NORIKO TABATA, DA-JUN YANG, HIROAKI TAKAYANAGI, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     8-epi-6-Deoxoblepharodol
C30H44O4     ÏàËÆ¶È:56.6%
Tetrahedron          2005          61          2513-2519
New phenolic triterpenes from Maytenus blepharodes. Semisynthesis of 6-deoxoblepharodol from pristimerin
F¨¦lix M. Rodr¨ªguez, Manuel R. L¨®pez, Ignacio A. Jim¨¦nez, Laila Moujir, Angel G. Ravelo, Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     3¦Â-O-sulfated-6¦Á-ol-cholest-9(11)-en-23-onesodium salt
C27H43O6SNa     ÏàËÆ¶È:55.5%
Journal of Chinese Pharmaceutical Sciences          2006          15          1-5
Sulfated Sterols Isolated from Starfish Asterias amurensis Lutken
LIU Hong-wei; LI Jian-kuan; WANG Nai-li; YAO Xin-sheng; and CAI Guo-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     compound 4
    ÏàËÆ¶È:55.5%
Acta Pharmaceutica Sinica          1994          29          200-203
ISOLATION AND IDENTIFICATION OF YIBEINOSIDE C FROM FRITILLAPIA PALLIDIFLORA
YJ Xu; DM Xu; DB Cui; JS Gao; Ex Huang; SY Liu and DQYu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     3¦Â-Acetoxy-17¦Â-[3-(N-4-chlorophenyl)-2-oxazolidon-5-yl]androst-5-ene
    ÏàËÆ¶È:55.5%
Steroids          2008          73          1375-1384
Neighboring group participation: Part 17 Stereoselective synthesis of some steroidal 2-oxazolidones, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase
D¨®ra Ondr¨¦, J¨¢nos Wölfling, Zolt¨¢n Iv¨¢nyi, Gyula Schneider, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     Lichuanine
C27H45NO2     ÏàËÆ¶È:55.5%
Journal of Asian Natural Products Research          2006          8          253-257
Two new steroidal alkaloids from bulbs of Fritillaria lichuanensis
H.-F. PI, H.-L. RUAN, Y.-H. ZHAN and J.-Z. WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     7-thiabrassinolide
C28H46O4S     ÏàËÆ¶È:55.5%
Phytochemistry          1998          49          1849-1858
Structure¨Cactivity studies of brassinolide B-ring analogues
Denise L. Baron, Weide Luo, Loeke Janzen, Richard P. Pharis, Thomas G. Back
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     budmunchiamine-A
C27H56N4O     ÏàËÆ¶È:55.5%
Phytochemistry          1996          42          1211-1215
Spermine alkaloids from Albizia schimperana
Geoffrey M. Rukunga, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     hookerianamides N
    ÏàËÆ¶È:55.5%
Planta Medica          2010          76          1022-1025
Bioactive Steroidal Alkaloids from Sarcococca hookeriana
Devkota, Krishna Prasad; Wansi, Jean D.; Lenta, Bruno N.; Khan, Samreen; Choudhary, Muhammad I.; Sewald, Norbert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     3¦Â-hydroxy-5¦Á-cholest-8(14),16-dien-15-one
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          1995          3          367-374
Chemical synthesis of 15-ketosterols and their inhibitions of cholesteryl ester transfer protein
Hong-Seok Kim, Sang Ho Oh, Dong-Il Kim, In-Chul Kim, Kyung-Hyun Cho, Yong Bok Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     N-{2-{3-[2-[(3-Indoly)ethyl]aminosulfonyl]phenylamino-carbonyl}ethyl}hexadecanoic acid amide
C35H52N3O4S     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2000          8          1991-2006
Design, synthesis and early structure¨Cactivity relationship of farnesyltransferase inhibitors which mimic both the peptidic and the prenylic substrate
Martin Schlitzer, Markus Böhm, Isabel Sattler, Hans-Martin Dahse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     17¦Á-allyl-17-hydroxy-3¦Â-(2-tetrahydropyranyl-oxy)androsta-5,15-diene
    ÏàËÆ¶È:55.5%
Russian Journal of Organic Chemistry          2007          43          1151-1157
Synthetic approach to preparation of indole derivatives fused with a bicyclo[3.3.1]nonane framework
A. V. Baranovskii, R. P. Litvinovskaya and V. A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     cycloart-24-en-3¦Â,26-diol
    ÏàËÆ¶È:55.5%
Chinese Journal of Natural Medicines          2012          10          36-39
Chemical constituents of Allophylus longipes
Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     ¦Â-sitosterol
    ÏàËÆ¶È:55.1%
Phytochemistry          2004          65          2463-2470
Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae)
Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     tetrahydroplakinamine A
C29H50N2     ÏàËÆ¶È:55.1%
Journal of Natural Products          2002          65          1206-1209
Minor Steroidal Alkaloids from the Marine Sponge Corticium sp.
Nicola Borbone,Simona De Marino,Maria Iorizzi, Franco Zollo, Cecile Debitus, Giuseppe Esposito, and Teresa Iuvone
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     stigmasterol
C29H28O     ÏàËÆ¶È:55.1%
Chemistry of Natural Compounds          2004          40          87-88
BIOLOGICALLY ACTIVE COMPOUNDS FROM Climacoptera
B. K. Eskalieva, A. Akhmed, G. Sh. Burasheva,Zh. A. Abilov, and V. U. Akhmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     (25R)-23-nitroamin-5,23-dien-3¦Â-ol acetate
    ÏàËÆ¶È:55.1%
Steroids          2008          73          657-668
Mechanistic insights and new products of the reaction of steroid sapogenins with NaNO2 and BF3¡¤Et2O in acetic acid
Yliana L¨®pez, Karen M. Ru¨ªz-P¨¦rez, Rebeca Y¨¦pez, Rosa Santillan, Marcos Flores-Alamo, Mart¨ªn A. Iglesias-Arteaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     plakinamine A
    ÏàËÆ¶È:55.1%
Journal of Natural Products          1994          Vol 57          1004
Two Steroidal Alkaloids from a Sponge, Corticium Sp.
Jaroslaw Jurek, Paul J. Scheuer, Michelle Kelly-Borges
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     wilforol B
C29H36O4     ÏàËÆ¶È:55.1%
Phytochemistry          1995          39          1159-1163
D:A-friedo-24-noroleanane triterpenoids from Tripterigium wilfordii
Takashi Morota, Chun-Xin Yang, Tatsunori Ogino, Wan-Zhang Qin, Takao Katsuhara, Li-Hong Xu, Yasuhiro Komatsu, Kang-Li Miao, Masao Maruno, Bing-Hui Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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