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²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (-)-regiolone C10H10O3 ÏàËÆ¶È:63.6% Phytochemistry 1988 27 3929-3932 (− -Regiolone,an ¦Á-tetralone from Juglans regia: structure,stereochemistry and conformationSunil K. Talapatra,Bimala Karmacharya,Shambhu C. De,Bani Talapatra Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

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-Regiolone,an ¦Á-tetralone from Juglans regia: structure,stereochemistry and conformation