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danil1288
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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-08-26 20:24:37
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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-08-26 20:24:37
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²éѯ½á¹û£º¹²²éµ½480¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . indole-3-acetic acid ÏàËÆ¶È:90% Natural Product Research and Development 2009 21 379-381 Compounds from Culture Broth of Paenibacillus polymyxa HY96-2 GONG Chun-yan; ZHANG Dao-jing; WEI Hong-gang; LI Shu-lan; SHEN Guo-min; LI Yuan-guang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Tryptophol[2-(3-indolyl)-ethanol] ÏàËÆ¶È:80% Biochemical Systematics and Ecology 2006 34 453-456 Indole alkaloids from a sponge Sarcotragus species Yonghong Liu, Jee H. Jung, Si Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound C25H19N3 ÏàËÆ¶È:80% Journal of Heterocyclic Chemistry 2009 46 535-539 A new catalytic method for ecofriendly synthesis of bis-and trisindolylmethanes by zirconyldodecylsulfate under mild conditions Maasoumeh Jafarpour,Abdolreza Rezaeifard and Tayebeh Golshani Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-¼×»ù-1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:80% Modern Chinese Medicine 2008 10(12) 29-31 Studies on the Metabolites of Salvianolic Acid B Yuan Zheng, Li Guoyu, , Zeng Yimei, Wang Jinhui Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . tris(1H-indol-3-yl)methane C25H19N3 ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 2010 18 6905-6913 Synthesis and cytotoxic potency of novel tris(1-alkylindol-3-yl)methylium salts: Role of N-alkyl substituents Sergey N. Lavrenov, Yuriy N. Luzikov, Evgeniy E. Bykov, Marina I. Reznikova, Evgenia V. Stepanova, Valeria A. Glazunova, Yulia L. Volodina, Victor V. Tatarsky Jr., Alexander A. Shtil, Maria N. Preobrazhenskaya Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-indolelactic acid methyl ester C12H13NO3 ÏàËÆ¶È:75% Heterocycles 2007 72 91-94 A New Method for Efficient Coupling of Indole and Epoxide Catalyzed with Yb(OTf)3, and Application to the Total Synthesis of Kurasoin B Satoshi Tsuchiya, Toshiaki Sunazuka, Tatsuya Shirahata, Tomoyasu Hirose, Eisuke Kaji, and Satoshi Omura Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 6 ÏàËÆ¶È:75% Heterocycles 2000 53 37-48 Preparation of Lavendamycin Analogues Christine Barbier, Arnaud Joissains, Alain Commerçon, Jean-François Riou, and François Huet* Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (¡À)-indollactic acid methyl ester C12H13NO3 ÏàËÆ¶È:75% The Journal of Antibiotics 1996 49 886-889 Kurasoins A and B, New Protein Earnesyltransferase Inhibitors Produced by Paedlomyces sp. FO-3684 II. Structure Elucidation and Total Synthesis RYUJI UCHIDA, KAZURO SHIOMI, TOSHIAKI SUNAZUKA, JUNJI INOKOSHI, AI NISHIZAWA, TOMOYASU HIROSE, HARUO TANAKA, YUZURU IWAI, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N,N-dimethyltryptamine-N-oxide ÏàËÆ¶È:72.7% Magnetic Resonance in Chemistry 2007 45 359-361 NMR spectral assignments of a new chlorotryptamine alkaloid and its analogues from Acacia confusa (pages 359¨C361) Malcolm S. Buchanan, Anthony R. Carroll, David Pass and Ronald J. Quinn Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,2'-thiobis(1H-indole-3-propanamide) C22H22N4O2S ÏàËÆ¶È:72.7% Journal of Medicinal Chemistry 1994 37 598-609 Tyrosine kinase inhibitors. 2. Synthesis of 2,2'-dithiobis(1H-indole-3-alkanamides) and investigation of their inhibitory activity against epidermal growth factor receptor and pp60v-src protein tyrosine kinases Andrew M. Thompson, David W. Fry, Alan J. Kraker, William A. Denny Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2,5-bis(3-indolylmethyl)pyrazine C22H18N4 ÏàËÆ¶È:70% Journal of Natural Products 2002 65 1660-1663 Pharacine, a Natural p-Cyclophane and Other Indole Derivatives from Cytophaga sp. Strain AM13.11 Mohamed Shaaban,Rajendra P. Maskey, Irene Wagner-Döbler, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . corynantheine ÏàËÆ¶È:70% Journal of Natural Products 1985 Vol 48 571-580 Chemistry of the Annonaceae, Part 18. Benzylated Indoles and Dihydrochalcones in Uvaria angolensis from Tanzania Ilias Muhammad, Peter G. Waterman |

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