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bin85666666: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-23 15:36:33
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°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 14.5,20.8,22.4,22.8,22.9,28.5,39.9,43.7,49.6,60.5,78.3,118.6,120.9,127.6,131.3,136.6,157.2,167.4 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½147¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . sydonic acid C15H22O4 ÏàËÆ¶È:72.2% Agricultural and Biological Chemistry 1978 42 37-40 Two New Metabolites, Sydonic Acid and Hydroxysydonic Acid, from Aspergillus sydowi Takashi HAMASAKI, Kouzou NAGAYAMA, Yuichi HATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (S)-(+)-11-dehydrosydonic acid C15H20O4 ÏàËÆ¶È:66.6% Journal of Natural Products 2010 73 911-914 Cytotoxic Polyphenols from the Marine-Derived Fungus Penicillium expansum Zhenyu Lu, Huajie Zhu, Peng Fu, Yi Wang, Zhihua Zhang, Haipeng Lin, Peipei Liu, Yibin Zhuang, Kui Hong and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (7S,11S)-(+)-12-acetoxysydonic acid C17H24O6 ÏàËÆ¶È:66.6% Journal of Natural Products 2010 73 911-914 Cytotoxic Polyphenols from the Marine-Derived Fungus Penicillium expansum Zhenyu Lu, Huajie Zhu, Peng Fu, Yi Wang, Zhihua Zhang, Haipeng Lin, Peipei Liu, Yibin Zhuang, Kui Hong and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (+)-sydonic acid C15H22O4 ÏàËÆ¶È:66.6% Bioscience, Biotechnology, and Biochemistry 2009 73 203-204 Isolation and Absolute Stereochemistry of Optically Active Sydonic Acid from Glonium sp. (Hysteriales, Ascomycota) Shinji KUDO, Takanori MURAKAMI, Junsuke MIYANISHI, Kazuaki TANAKA, Noboru TAKADA and Masaru HASHIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 1 C19H24N2O2 ÏàËÆ¶È:63.1% Natural Product Research 1998 12 293-298 19(R)-Hydroxyeburnamine and 19(R)-Hydroxy-Isoeburnamine from Kopsia Dasyrachis Toh-Seok Kam; G. Subramaniam; Chen Wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ( + )-19 (R)-hydroxyeburnamine C19H24N2O2 ÏàËÆ¶È:63.1% Phytochemistry 1999 51 159-169 Alkaloids from Kopsia dasyrachis Toh-Seok Kam, G. Subramaniam, Wei Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . expansol G C17H24O6 ÏàËÆ¶È:61.1% Chinese Journal of Marine Drugs 2012 31 7-13 Secondary metabolites and their bioactivities of a soft coral-derived fungus Aspergillus versicolor(ZJ-2008015) ZHENG Cai-juan; SHAO Chang-lun; WANG Kai-ling; ZHAO Dong-lin; WANG Ya-nan; WANG Chang-yun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . laur-11-en-1,10-diol C15H20O2 ÏàËÆ¶È:55.5% Journal of Natural Products 2005 68 915-919 Sesquiterpenes from the Red Alga Laurencia tristicha Jie Sun, Dayong Shi, Ming Ma, Shuai Li, Sujuan Wang, Lijun Han, Yongchun Yang,Xiao Fan,Jiangong Shi,and Lan He Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 7,12,13-trihydroxybisabola-3,10-diene C15H26O3 ÏàËÆ¶È:55.5% Journal of Natural Products 2005 68 1805-1808 Bisabolane- and Santalane-Type Sesquiterpenoids from Santalum album of Indian Origin Tae Hoon Kim, Hideyuki Ito, Tsutomu Hatano, Toshio Hasegawa,Aiko Akiba, Takahisa Machiguchi, and Takashi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (+)-(7S)-7-O-Methylsydonic acid C16H24O4 ÏàËÆ¶È:55.5% Journal of Natural Products 2011 84 1663-1667 Sesquiterpene and Xanthone Derivatives from the Sea Fan-Derived Fungus Aspergillus sydowii PSU-F154 Kongkiat Trisuwan, Vatcharin Rukachaisirikul, Morakot Kaewpet, Souwalak Phongpaichit, Nongporn Hutadilok-Towatana, Sita Preedanon, and Jariya Sakayaroj Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (10a'S)-2',3',5',6',7',10'-Hexahydro-10a'H-spiro[1,3-dithiolane-2,1'-pyrrolo[1,2-a]azocine]-10a'-carboxylic acid ethyl ester C15H23NO2S2 ÏàËÆ¶È:55.5% Heterocycles 2006 68 47-58 Concise Highly Enantioselective Cascade Synthesis of Azacyclooctene Alkaloids with a Quaternary Stereocenter Daniele Muroni, Antonio Saba,* and Nicola Culeddu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 3d ÏàËÆ¶È:55.5% Tetrahedron Letters 2002 43 4399-4402 Synthesis of ¦Â-organotelluro vinylphosphine oxides by hydrotelluration of 1-alkynylphosphine oxides and their palladium-catalyzed cross-coupling with alkynes Antonio L. Braga, Fabrı́cio Vargas, Gilson Zeni, Claudio C. Silveira, Leandro H. de Andrade Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (S)-methyl 2-(pentylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate C19H25N3O3 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2011 19 6182-6195 Design, synthesis, and biological evaluation of callophycin A and analogues as potential chemopreventive and anticancer agents Li Shen, Eun-Jung Park, Tamara P. Kondratyuk, Daniela Guendisch, Laura Marler, John M. Pezzuto, Anthony D. Wright, Dianqing Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (R)-methyl 2-(pentylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate C19H25N3O3 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2011 19 6182-6195 Design, synthesis, and biological evaluation of callophycin A and analogues as potential chemopreventive and anticancer agents Li Shen, Eun-Jung Park, Tamara P. Kondratyuk, Daniela Guendisch, Laura Marler, John M. Pezzuto, Anthony D. Wright, Dianqing Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 16 C16H27N3 ÏàËÆ¶È:55.5% Tetrahedron 1995 51 10913-10922 Short syntheses of (¡À)-tetraponerines-5 and -6. the structures of tetraponerines-1 and -2, and a revision of the structures of (+)-tetraponerines-5 and -6 Christine Devijver, Pascale Macours, Jean-Claude Braekman, D¨¦sir¨¦ Daloze, Jacques M. Pasteels Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . cyclo(L-Leu-L-Trp) C17H21N3O2 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2012 20 2002-2009 Cyclic dipeptides exhibit potency for scavenging radicals Tadashi Furukawa, Takashi Akutagawa, Hitomi Funatani, Toshikazu Uchida, Yoshihiro Hotta, Masatake Niwa, Yoshiaki Takaya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . N-[5-iodo-2-(tert-butylamino)benzoyl]-3(S)-aminobutanoic acid,ethyl ester C17H26N2O3I ÏàËÆ¶È:55.5% Journal of Medicinal Chemistry 1997 40 717-729 From Peptide to Non-Peptide. 3. Atropisomeric GPIIbIIIa Antagonists Containing the 3,4-Dihydro-1H-1,4-benzodiazepine-2,5-dione Nucleus Brent K. Blackburn, Arthur Lee, Mark Baier, Benjamin Kohl, Alan G. Olivero, Regina Matamoros, Kirk D. Robarge, and Robert S. McDowell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 8¦Á,15-Epoxylabdan-16¦Â-oic acid C20H34O3 ÏàËÆ¶È:55% Phytochemistry 2010 71 798-803 8,15-Epoxylabdane and norlabdane diterpenoids from Eragrostis viscosa N¡¯Soki N. Sebastião, In¨ºs J.S. Cordeiro, Aldenir F. dos Santos, Jorge F. Gaspar, C¨¦lia Martins, Jos¨¦ Rueff, Carlos Diakanamwa, Antônio E.G. Sant¡¯Ana, Dina I.M.D. de Mendonça Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 1¦Â,9¦Â-Diacetoxyeudesm-3-en-5¦Á,6¦Â,11¦ÂH-12,6-olide C15H18O2 ÏàËÆ¶È:52.6% Phytochemistry Letters 2008 1 85-88 Sesquiterpene lactones from Algerian Artemisia herba-alba Messai Laid, Mohamed-Elamir F. Hegazy, Ahmed A. Ahmed, Kalla Ali, Djaballah Belkacemi, Shinji Ohta Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 11 C21H31N3O2 ÏàËÆ¶È:52.6% Chinese Chemical Letters 2010 21 889-891 First total synthesis of eudistalbin A Pu Yong Zhang; Jun Lei Wang; Sheng Biao Wan; Tao Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 9d ÏàËÆ¶È:52.6% Tetrahedron Letters 2005 46 5999-6003 TiCl4-promoted addition of nucleophiles to open chain ¦Á-amidoalkylphenyl sulfones Marino Petrini, Elisabetta Torregiani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . O-[(1aS*,2aS*,5R*,5aR*,7aS*)-7a-(hydroxymethyl)-5-iso-propyl-5a-methyloctahydroazuleno[5,6-b]oxiren-3(1aH)-one]Imidazol-1-yl thiocarbonate C19H26N2O3S ÏàËÆ¶È:52.6% The Journal of Organic Chemistry 2010 75 8337-8350 Construction of the Tricyclic 5−7−6 Scaffold of Fungi-Derived Diterpenoids. Total Synthesis of (¡À)-Heptemerone G and an Approach to Danishefsky¡¯s Intermediate for Guanacastepene A Synthesis Karol Michalak, Michał Michalak, and Jerzy Wicha Structure 13C NMR ̼Æ×Ä£Äâͼ |

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