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2Â¥2013-08-21 18:54:59
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fly5fish

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2Â¥: Originally posted by lifeliuyan at 2013-08-21 18:54:59
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19.2,21.6,22.2,22.9,24.5,24.8,27.4,27.6,28.7,31.2,31.6,33.4,38.3,39.4,58.4,72.1,
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61.9,68.3,77.1,129.3,131.3,169.9,170.1
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3Â¥2013-08-21 22:37:33
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1 .     (1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol
C20H34O3     ÏàËÆ¶È:65%
Phytochemistry          2008          69          2844-2848
Oxygenated verticillene derivatives from Bursera suntui
Hugo A. Garc¨ªa-Guti¨¦rrez, Carlos M. Cerda-Garc¨ªa-Rojas, Juan D. Hern¨¢ndez-Hern¨¢ndez,Luisa U. Rom¨¢n-Mar¨ªn, Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     mulinenic
    ÏàËÆ¶È:65%
Phytochemistry          1996          43          165-168
Mulinolic acid, a diterpenoid from Mulinum crassifolium
Luis A. Loyola, Jorge B¨®rquez, Glauco Morales, Aurelio San Mart¨ªn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     13¦Â,17-epoxymulin-11-en-20-oic acid
C20H30O3     ÏàËÆ¶È:65%
Journal of Natural Products          1991          Vol 54          1404
Mulinenic Acid, a Rearranged Diterpenoid from Mulinum crassifolium
Luis A. Loyola, Glauco Morales, Benjamin Rodriguez, Jesus Jimenez-Barbero, Samuel Pedreros, Maria C. de la Torre, Aurea Perales
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     3,7,11,15-tetramethyl-hexadecan-1,3-diol
    ÏàËÆ¶È:65%
Chinese Traditional and Herbal Drugs          2007          38          1779-1782
Acyclic diterpenoids and aliphatic compounds from green alga Chaetomorpha basiretorsa and their activities
SHI Da-yong; HAN Li-jun; SUN Jie; YANG Yong-chun; SHI Jian-gong; FAN Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 11
    ÏàËÆ¶È:65%
Tetrahedron Letters          2003          44          1871-1873
Design, synthesis and evaluation of new RDP inhibitors
Hallur Gurulingappa, Phillip Buckhaults, Srinivas K. Kumar, Kenneth W. Kinzler, Bert Vogelstein, Saeed R. Khan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (1S,2E,4R,6E,8S,11S,12S)-2,6-cembradiene-4,8,11,12-tetrol
    ÏàËÆ¶È:65%
Acta Chemica Scandinavica          1986          40          123-134
Tobacco Chemistry. 69. Five New Labdanic Compounds from Tobacco.
Wahlberg, Inger; Eklund, Ann-Marie; Nordfors, Kerstin; Vogt, Carmen; Enzell, Curt R.; Berg, Jan-Eric
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (-)-lepadiformine A
C19H35NO     ÏàËÆ¶È:65%
European Journal of Organic Chemistry          2010                   1660-1668
Total Synthesis of (¨C)-Fasicularin and (¨C)-Lepadiformine A Based on Zn-Mediated Allylation of Chiral N-tert-Butanesulfinyl Ketimine
San-Lin Mei and Gang Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     2¦Â,3¦Á-dihydroxy-trinervita-1(15),8(19)-diene
C20H32O2     ÏàËÆ¶È:65%
Natural Product Communications          2013          8          69-74
Chemical Composition and Biological Activities of Soldiers of the Brazilian Termite Species, Nasutitermes macrocephalus (Isoptera: Natutitermitinae)
M¨¢rcia N. S. de la Cruz, Helv¨¦cio M. S. J¨²nior, Denilson F. Oliveira, Let¨ªcia V. Costa-Lotufo, Antonio G. Ferreira, Daniela S. Alviano and Claudia M. Rezende
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     [(1R,3aS,4R,7aR)-1-((R)-1,5-dimethylhexyl)-7a-methylhexahydrocyclopropa[d]inden-4-yl-oxy]-trimethylsilane
    ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry          2013          21          1925-1943
Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase
Mathias König, Christoph M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (6aR,10aS)-4-isopropyl-2,2,7,7,10a-pentamethyl-6a,7,8,9,10,10a-hexahydro-6H-1,3-dioxacyclopenta[c]fluorene
C22H32O2     ÏàËÆ¶È:63.6%
Tetrahedron          2013          69          3841-3846
First asymmetric total synthesis of (+)-taiwaniaquinol D and (−-taiwaniaquinone D by using intramolecular Heck reaction
Minoru Ozeki, Megumi Satake, Toshinori Toizume, Shintaro Fukutome, Kenji Arimitsu, Shinzo Hosoi, Tetsuya Kajimoto, Hiroki Iwasaki, Naoto Kojima, Manabu Node, Masayuki Yamashita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (13R,14R,17R)-3¦Â,17-dihydroxy-14-acetoxy-13,14-seco-androst-5-ene
    ÏàËÆ¶È:61.9%
Steroids          2004          69          501-509
Synthesis of 13,14-secotestosterone derivatives
Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Yuliya Y. Zhiburtovich, Galina P. Fando, 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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12 .     Kalihinol J
C22H35ClN2O3S     ÏàËÆ¶È:61.9%
Tetrahedron          2004          60          6981-6988
Kalihinols from two Acanthella cavernosa sponges: inhibitors of bacterial folate biosynthesis
Tim S. Bugni, Maya P. Singh, Lei Chen, Daniel A. Arias, Mary Kay Harper, Michael Greenstein, William M. Maiese, Gisela P. Concepci¨®n, Gina C. Mangalindan, Chris M. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     9¦Â-hydroxydarutigenol
C20H34O4     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          2005-2008
ent-Pimarane Diterpenoids from Siegesbeckia orientalis and Structure Revision of a Related Compound
Fei Wang, Xue-Lian Cheng, Ya-Ju Li, Song Shi, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5-epipisiferol
    ÏàËÆ¶È:60%
Phytochemistry          2007          68          210-217
Antibacterials and modulators of bacterial resistance from the immature cones of Chamaecyparis lawsoniana
Eileen C.J. Smith, Elizabeth M. Williamson, Neale Wareham,Glenn W. Kaatz, Simon Gibbons
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     mulin-12-ene-14-one-20-oic acid
C20H30O3     ÏàËÆ¶È:60%
Phytochemistry          2003          63          883-886
Mulinane-type diterpenoids from Mulinum spinosum
Alejandra I. Chiaramello, Carlos E. Ardanaz, Eduardo E. Garc¨ªa,Pedro C. Rossomando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     lepadiformine B
C17H31NO     ÏàËÆ¶È:60%
Journal of Natural Products          2006          69(4)          558-562
Sensitivity of Cardiac Background Inward Rectifying K Outward Current (IK1) to the Alkaloids Lepadiformines A, B, and C
Martin-Pierre Sauviat, Joseph Vercauteren, Nicole Grimaud, Marcel Jug, Mohamed Nabil, Jean-Yves Petit, and Jean-Franois Biard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     sargachromanol N
C27H38O3     ÏàËÆ¶È:60%
Journal of Natural Products          2005          68          716-723
Chromenes from the Brown Alga Sargassum siliquastrum
Kyoung Hwa Jang, Bong Ho Lee, Byoung Wook Choi, Hyi-Seung Lee, and Jongheon Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 1a/1b
C38H78NO5     ÏàËÆ¶È:60%
Journal of Natural Products          2001          64          1210-1215
Sex Pheromones of the Hair Crab Erimacrus isenbeckii. II. Synthesis of Ceramides
Naoki Asai, Nobuhiro Fusetani, and Shigeki Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 2
    ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          978-980
(2R,3R,7Z)-2-Aminotetradec-7-ene-1,3-diol, a New Amino Alcohol from the Caribbean Sponge Haliclona vansoesti
C. Devijver, M. Salmoun, D. Daloze, J. C. Braekman, W. H. De Weerdt, M. J. De Kluijver, and R. Gomez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     florlide B
C20H30O4     ÏàËÆ¶È:60%
Journal of Natural Products          1998          61          1513-1515
New Xenia Diterpenes Isolated from the Soft Coral, Xenia florida
Tetsuo Iwagawa, Jun-ichi Kawasaki, and Tsunao Hase
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2013-08-22 08:23:46
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fly5fish: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-08-22 10:49:12
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1 .     methyl-8¦ÂH-9¦Á-hydroxylabda-13Z-en-15-oate
C21H36O3     ÏàËÆ¶È:65.2%
Phytochemistry          1991          30          211-213
Diterpenes from Leyssera gnaphaloides
F. Tsichritzis, J. Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 3
    ÏàËÆ¶È:65.2%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     9¦Á,10¦Â-diacetoxy-5¦Á,-13¦Á-dihydroxy-¦Á-4,20:11,12-diepoxytaxane
C24H36O8     ÏàËÆ¶È:62.5%
Journal of Natural Products          2004          67          2136-2140
New Regio- and Stereoselective O-Deacetylated and Epoxy Products of Taxanes Isolated from Taxus mairei
Ya-Ching Shen, Chin-Lien Ko, Yuan-bin Cheng, Michael Y. Chiang, and Ashraf Taha Khalil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 2
    ÏàËÆ¶È:62.5%
Chemical & Pharmaceutical Bulletin          1996          44          1540-1545
Studies on Nepalese Crude Drugs. XXXI. On the Diterpenoid Constituents of the Aerial Part of Scutellaria discolor COLEBR.
Akiko OHNO,Haruhisa KIZU and Tsuyoshi TOMIMORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     15,16-di-O-acetyl-2,7-dioxofagonene
C24H34O6     ÏàËÆ¶È:62.5%
Phytochemistry          1994          36          1431-1433
Erythroxan diterpenes from Fagonia species
Maged S. Abdel-Kader, Abdallah A. Omar, Nabil A. Abdel-Salam, Frank R. Stermitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     5¦Â,6¦Â-epoxy-3¦Â-hydroxy-17-oxad-homoandrostane-16-one + 5¦Á,6¦Á-epoxy-3¦Â-hydroxy-17-oxad-homoandrostane-16-one
    ÏàËÆ¶È:61.5%
Steroids          2008          73          681-688
Synthesis and biological evaluation of some new A,B-ring modified steroidal d-lactones
Evgenija A. Djurendić, Marija N. Sakač, Marina P. Zaviš, Andrea R. Gaković, Janoš J. Čanadi, Silvana A. Andrić, Olivera R. Klisurić, Vesna V. Kojić, Gordana M. Bogdanović, Katarina M. Penov Gaši
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     viteagnusin D
C20H36O2     ÏàËÆ¶È:60.8%
Chemical & Pharmaceutical Bulletin          2008          56(11)          1621-1624
Five New Diterpenoids, Viteagnusins A¡ªE, from the Fruit of Vitex agnus-castus
Masateru ONO,Toru YAMASAKI,Masatarou KONOSHITA,Tsuyoshi IKEDA,Masafumi OKAWA,Junei KINJO,Hitoshi YOSHIMITSU,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     3¦Â,16¦Á-Diacetoxy-5¦Á-androstan-17-on-(Z)-oxim
C23H35NO5     ÏàËÆ¶È:60.8%
Helvetica Chimica Acta          1980          63          1562-1581
Steroide und Sexualhormone. 261. Mitteilung. Quassinoide Bitterstoffe II. Partialsynthetischer Zugang zu Quassin: Überf¨¹hrung von Testosteron in eine Schl¨¹sselverbindung mit angulärer 8¦Â-Methylgruppe
Johannes Pfenninger, Walter Graf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     3¦Â,16¦Â-Diacetoxy-5¦Á-androstan-l7-on-(Z)-oxim
C23H35NO5     ÏàËÆ¶È:60.8%
Helvetica Chimica Acta          1980          63          1562-1581
Steroide und Sexualhormone. 261. Mitteilung. Quassinoide Bitterstoffe II. Partialsynthetischer Zugang zu Quassin: Überf¨¹hrung von Testosteron in eine Schl¨¹sselverbindung mit angulärer 8¦Â-Methylgruppe
Johannes Pfenninger, Walter Graf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     methyl 15-aeeto xy-2-oxo-1(10)-ent-halimen-18-oate
    ÏàËÆ¶È:60.8%
Phytochemistry          1997          44          1301-1307
Hydrohalimic acids from Halimium viscosum
Dina I. M. D. de Mendonça, Jesus M. L. Rodilla, Anna M. Lithgow, Isidro S. Marcos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     compound 21
    ÏàËÆ¶È:60.8%
Phytochemistry          1996          41          1129-1141
Ent-kaurane-type diterpenoids from the liverwort Jungermannia exsertifolia ssp. Cordifolia
Fumihiro Nagashima, Hironao Tanaka, Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     Methyl thyrsiflorin B acetate
C26H40O6     ÏàËÆ¶È:60.8%
Phytochemistry          1995          40          1751-1754
Diterpenoids from calceolaria dentata
M. C. Chamy, M. Piovano, J. A. Garbarino, C. Vargas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Dihydro-¦Á-santalyl formate
C16H26O2     ÏàËÆ¶È:60.8%
Molecules          2012          17          2259-2270
Structure-Odor Relationships of ¦Á-Santalol Derivatives with Modified Side Chains
Toshio Hasegawa , Hiroaki Izumi , Yuji Tajima and Hideo Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 9
    ÏàËÆ¶È:60.8%
Organic letters          2002          4          2783-2785
Elusive 6-exo-Hydroxybicyclo[2.2.2]octan-2-ones from the Corresponding Acetates by Methanolysis in the Presence of CH3ONa/La(OTf)3
Stefano Di Stefano, Francesca Leonelli, Barbara Garofalo, Luigi Mandolini, Rinaldo Marini Bettolo, and Luisa Maria Migneco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     Compound 6
    ÏàËÆ¶È:60.8%
Magnetic Resonance in Chemistry          2005          43          877-880
1H and 13C NMR signal assignment of synthetic (-)-methyl thyrsiflorin B acetate, (-)-thyrsiflorin C and several scopadulane derivatives
Miguel A. Gonz¨¢lez and Ram¨®n J. Zaragoz¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 2
    ÏàËÆ¶È:60.8%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     compound 25
C22H30O4     ÏàËÆ¶È:60.8%
Tetrahedron          2005          61          4531-4544
Novel cytotoxic kaurane-type diterpenoids from the New Zealand Liverwort Jungermannia species
Fumihiro Nagashima, Masuo Kondoh, Makiko Fujii, Shigeru Takaoka, Yoshiteru Watanabe, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     paxdaphnidine B
C22H35NO2     ÏàËÆ¶È:60.8%
The Journal of Organic Chemistry          2004          69          1726-1729
Paxdaphnidines A and B, Novel Penta-and Tetracyclic Alkaloids from Daphniphyllum paxianum
Zha-Jun Zhan, Sheng-Ping Yang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 6
C22H38O4     ÏàËÆ¶È:60.8%
Tetrahedron          1995          51          5291-5298
Irregular cembranoids containing a 13-membered carbocyclic skeleton isolated from a soft coral, Sarcophyton species
Tetsuo Iwagawa, Shun Nakamura, Takahiro Masuda, Hiroaki Okamura, Munehiro Nakatani, Motto Siro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     11¦Â,5¦Á-diacetoxysilphinen-3-one
C19H26O5     ÏàËÆ¶È:60.8%
Journal of Chemical Ecology          2002          28          117-129
Silphinene Sesquiterpenes as Model Insect Antifeedants
Azucena Gonz¨¢lez-Coloma, Fernando Valencia, Nuria Mart¨ªn, Joseph J. Hoffmann, Louis Hutter, J. Alberto Marco, Mat¨ªas Reina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     24R-methylcholesta-3¦Â,5¦Á,6¦Â-triol
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