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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2013-10-25 13:08:30
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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2013-10-25 13:08:30
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²éѯ½á¹û£º¹²²éµ½429¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . indole-3-acetic acid ÏàËÆ¶È:83.3% 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 . methyl 3,3-di(1H-indol-3-yl)propanoate C20H18N2O2 ÏàËÆ¶È:76.9% Tetrahedron 2013 69 1600-1605 TFA-catalyzed C¨CN bond activation of enamides with indoles: efficient synthesis of 3,3-bisindolylpropanoates and other bisindolylalkanes Hai-Yan Xu, You Zi, Xiao-Ping Xu, Shun-Yi Wang, Shun-Jun Ji Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 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 4 . 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 5 . 1H-indole-3-carboxylic acid C9H7O2N ÏàËÆ¶È:75% Research in Microbiology 2010 161 335-345 Purification and biological evaluation of the metabolites produced by Streptomyces sp. TK-VL_333 Alapati Kavitha, Peddikotla Prabhakar, Muvva Vijayalakshmi, Yenamandra Venkateswarlu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (¡À)-2-hydroxy-3-(3-indolyl)-N-methoxy-N-methyl-propanamide C13H16N2O3 ÏàËÆ¶È:69.2% 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 7 . methyl 3,3-bis(7-methyl-1H-indol-3-yl)propanoate C22H22N2O2 ÏàËÆ¶È:69.2% Tetrahedron 2013 69 1600-1605 TFA-catalyzed C¨CN bond activation of enamides with indoles: efficient synthesis of 3,3-bisindolylpropanoates and other bisindolylalkanes Hai-Yan Xu, You Zi, Xiao-Ping Xu, Shun-Yi Wang, Shun-Jun Ji Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . methyl Indol-3-ylacetate C11H11NO2 ÏàËÆ¶È:66.6% Journal of Natural Products 2003 66 183-199 Synthesis and Antimitotic/Cytotoxic Activity of Hemiasterlin Analogues James A. Nieman, John E. Coleman, Debra J. Wallace, Edward Piers, Lynette Y. Lim, Michel Roberge, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ |
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