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1 .     cis-isoshinanolone
C11H12O3     ÏàËÆ¶È:100%
Phytochemist ...

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1 .     cis-isoshinanolone
C11H12O3     ÏàËÆ¶È:100%
Phytochemistry          1999          51          693-699
Cis- and trans-isoshinanolone from Dioncophyllum thollonii: absolute configuration of two 'known', wide-spread natural products
Gerhard Bringmann, Miriam Munchbach, Kim Messer, Dagmar Koppler, Manuela Michel, Olaf Schupp, Matthias Wenzel, Adriaan M. Louis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (+ )-isoshinanolone
C11H12O3     ÏàËÆ¶È:100%
Phytochemistry          1981          20          1162-1164
(+)-Isoshinanolone and 2-methylbenzofuran-4-carbaldehyde from the fish-stunning plant Habropetalum dawei
Steven W. Hanson, Malcolm Crawford, Devavaram P. J. Thanasingh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     isoshinanolone
    ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2012          37          222-225
Study on chemical constituents of Drosera peltata var. multisepala
LI Lin; HUANG Jin; XU Xianghua; ZHANG Yao; CHENG Kejun; YU Peizhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     DG-5
C10H10O3     ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          1998          46          423-429
Immunosuppressive Components from an Ascomycete, Diplogelasinospora grovesii
Haruhiro FUJIMOTO,Junko NAGANO,Kentaro YAMAGUCHI and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (-)-regiolone
C10H10O3     ÏàËÆ¶È:63.6%
Phytochemistry          1988          27          3929-3932
(−-Regiolone,an ¦Á-tetralone from Juglans regia: structure,stereochemistry and conformation
Sunil K. Talapatra,Bimala Karmacharya,Shambhu C. De,Bani Talapatra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Isosclerone
    ÏàËÆ¶È:63.6%
Archives of Pharmacal Research          2012          35          1127-1131
Metabolites from the mangrove-derived fungus Xylaria cubensis PSU-MA34
Saranyoo Klaiklay, Vatcharin Rukachaisirikul, Yaowapa Sukpondma, Souwalak Phongpaichit and Jirayu Buatong, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (-)-isosclerone
C14H16N2O3S2     ÏàËÆ¶È:63.6%
Marine Drugs          2012          10          2912-2935
Isolation, Structure Elucidation and Total Synthesis of Lajollamide A from the Marine Fungus Asteromyces cruciatus
Tobias A. M. Gulder, Hanna Hong, Jhonny Correa, Ekaterina Egereva, Jutta Wiese, Johannes F. Imhoff and Harald Gross
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     cis-(3RS,4SR)-3,4-Dihydro-3,4,8-trihydroxynaphthalen-1(2H)-one
    ÏàËÆ¶È:54.5%
Helvetica Chimica Acta          2009          92          903-917
Stereoselective Synthesis of cis- and trans-3,4-Dihydro-3,4,8-trihydroxynaphthalen-1(2H)-one
Emmanuel Couch¨¦, Abdellatif Fkyerat, Raffaele Tabacchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (4S)-3,4-dihydro-4,8-dihydroxy-l(2H)-naphthalenoe
C10H10O3     ÏàËÆ¶È:54.5%
Natural Product Research          2000          14          405-410
Metabolites from a Wood-Inhabiting Cup Fungus, Urnula craterium
William A. Ayer; Latchezar S. Trifonov; Leonard J. Hutchison; Priyotosh Chakravarty
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     3,4-Dihydro-3,4,8-trihydroxy-l(2H)-naphthalenone
C10H10O4     ÏàËÆ¶È:54.5%
Journal of Natural Products          1989          Vol 52          119
Metabolites of Leptographium wageneri, the Causative Agent of Black Stain Root Disease of Conifers
William A. Ayer, Lois M. Browne, Ge Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     2-Amino-1,6-dihydro-4-(3-hydroxyphenyl)-6-oxopyrimidine-5-carbonitrile
C11H8N4O2     ÏàËÆ¶È:54.5%
Helvetica Chimica Acta          2010          93          777-784
A Novel and Efficient One-Pot Synthesis of 2-Aminopyrimidinones and Their Self-Assembly
Morteza Bararjanian, Saeed Balalaie, Frank Rominger and Sanaz Barouti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     3,4-dihydro-3,4,8-trihydroxy-1(2H)-naphthalenone
C10H10O4     ÏàËÆ¶È:54.5%
Tetrahedron          1991          47          8351-8360
Isolation and structure elucidation of hymatoxins B - E and other phytotoxins from Hypoxylon mammatum fungal pathogen of leuce poplars
Katrin Borgschulte, Sylvie Rebuffat, Wolfram Trowitzsch-Kienast, Dietmar Schomburg, Jean Pinon, Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     2'-hydroxydihydrochalcone
C15H14O2     ÏàËÆ¶È:50%
Phytochemistry          1998          49          229-232
Phenolic compounds from peperomia obtusifolia
Toshiyuki Tanak¦Á, Fujio Asai, Munekazu Iinuma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5-Ethyl-2-(2-methoxycarbonyl-acetylamino)-thiophen-3-carboxylic acid methyl ester
    ÏàËÆ¶È:50%
Archives of Pharmacal Research          2001          24          270-275
4-Hydroxy-6-Oxo-6,7-Dihydro-Thieno[2,3-b] pyrimidine derivatives: Synthesis and their biological evaluation for the glycine site acting on the N -Methyl-D-aspartate (NMDA) receptor
Ki-Jun Hwang, Tae-Suk Lee, Ki-Won Kim, Beom-Tae Kim and Chul-Min Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     5a,6,8,9-Tetrahydro-5H-pyrido[2,1-b]quinazoline-7,11-dione
C12H12N2O2     ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          6725-6727
Synthesis of a piperidone model compound and revision of the structures of jenamidines A to C
Barry B. Snider, Jeremy R. Duvall, Isabel Sattler, Xueshi Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     ¦Â-Hydroxy-4-fluorodihydrochalcone
    ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2011          47          33-37
Synthesis of fluorine-containing 3-hydroxyflavanones and isoflavones
T. S. Khlebnikova, Yu. A. Piven', N. B. Khripach and F. A. Lakhvich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     compound 8
C12H12O4     ÏàËÆ¶È:50%
Natural Product Communications          2011          6          661-666
Bioactive Aromatic Derivatives from Endophytic Fungus, Cytospora sp.
Shan Lu, Siegfried Draeger, Barbara Schulz, Karsten Krohn, Ishtiaq Ahmed, Hidayat Hussain, Yanghua Yi, Ling Li, and Wen Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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