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xiaoxiao270: ½ð±Ò+4 2013-01-20 22:04:17
chzhbin: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-01-20 23:20:14
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xiaoxiao270: ½ð±Ò+4 2013-01-20 22:04:17
chzhbin: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-01-20 23:20:14
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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 22.46, 47.08, 49.57, 112.82, 112.95, 122.67, 123.30, 124.40, 134.25, 138.30, 191.88 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£º¹²²éµ½60¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . N-acetyl-¦Â-oxotryptamine C12H12N2O2 ÏàËÆ¶È:75% Molecules 2012 17 11146-11155 Antitrypanosomal Alkaloids from the Marine Bacterium Bacillus pumilus Sergio Mart¨ªnez-Luis, Jos¨¦ F¨¦lix G¨®mez, Carmenza Spadafora, H¨¦ctor M. Guzm¨¢n and Marcelino Guti¨¦rrez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3-bromo-6-iodocarbazole C12H7NBrI ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2001 38 77-87 Synthesis and isolation of iodocarbazoles. Direct iodination of carbazoles by N-iodosuccinimide and N-iodosuccinimide-silica gel system Sergio M. Bonesi and Rosa Erra-Balsells Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 4,5,6,7-Tetrachloro-2-(3,5-dimethylphenyl)-1,3-benzodioxole C15H10Cl4O2 ÏàËÆ¶È:54.5% Molecules 2002 7 840-847 First Example of Direct Transformation of Alkylbenzenes to 1, 3-Benzodioxoles by Oxidation with o-Chloranil Sheikh M. Rahman and Tomoshige Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3-ßÅßá¼×Ëá ÏàËÆ¶È:54.5% Chinese Journal of Marine Drugs 2000 19(1) 1-4 STUDIES ON THE CHEM ICAL CONSTITUTIONS OF THE SPONGE SUBERITES TYLOBTUSA LEV I Li Wenlin, Mao Shilong, Yi Yanghua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1-((4,5-Dihydro-1H-imidazol-2-yl)methyl)-5-methyl-1H-indazole C12H16Cl2N4 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2012 20 108-116 Synthesis and biological activities of 2-[(heteroaryl)methyl]imidazolines Jaroslaw Saczewski,Alan Hudson, Mika Scheinin,Apolonia Rybczynska, Daqing Ma,Franciszek Saczewski, Shayna Laird, Jonne M. Laurila, Konrad Boblewski,Artur Lehmann, Jianteng Gu, Helena Watts Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ÐØÏÙà×ठÏàËÆ¶È:54.5% Chinese Journal of Marine Drugs 2011 30(5) 12-17 Studies on the chemical constituents of sponge Haliclona cymaeformis from the South China Sea WU Xu-dong,MEI Wen-li,SHAO Chang-lun,Nicole J.de Voogd,WANG Hu,WANG Chang-yun,DAI Hao-fu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:54.5% Biochemical Systematics and Ecology 2012 43 210-213 Monoindole alkaloids from a marine sponge Mycale fibrexilis Ru-Ping Wang, Hou-Wen Lin, Ling-Zhi Li, Pin-Yi Gao, Ying Xu, Shao-Jiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 6-bromo-1H-indole-3-carboxylic acid ethyl ester ÏàËÆ¶È:54.5% Biochemical Systematics and Ecology 2012 43 210-213 Monoindole alkaloids from a marine sponge Mycale fibrexilis Ru-Ping Wang, Hou-Wen Lin, Ling-Zhi Li, Pin-Yi Gao, Ying Xu, Shao-Jiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 1H-indole-3-hydroxyacetyl ÏàËÆ¶È:54.5% Biochemical Systematics and Ecology 2012 43 210-213 Monoindole alkaloids from a marine sponge Mycale fibrexilis Ru-Ping Wang, Hou-Wen Lin, Ling-Zhi Li, Pin-Yi Gao, Ying Xu, Shao-Jiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-(hydroxyacetyl)indole ÏàËÆ¶È:54.5% Phytochemistry 1990 29 3697-3698 3-(Hydroxyacetyl)indole,a plant growth regulator from the oregon red alga Prionitis lanceolata Matthew Bernart,William H. Gerwick |
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