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13C NMR (101 MHz, Acetone) ¦Ä30.53,108.17,111.24,118.66,118.71,121.30,123.65,172.36 13C NMR (101 MHz, Acetone) ¦Ä 6.40,23.04,46.19,51.15,63.97,109.50,110.69,112.81,138.34,162.54,163.89,194.26,206.32 [ Last edited by ÐÐÎÞÈË on 2013-6-5 at 19:39 ] |
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²éѯ½á¹û£º¹²²éµ½3¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 2,4-dihydroxy-3-methyl-6-(2-oxopropyl)benzaldehyde C11H12O4 ÏàËÆ¶È:69.2% Journal of Heterocyclic Chemistry 2001 38 1409-1418 Synthesis of 7-acetyloxy-3,7-dimethy1-7,8-dihydro-6H-isochromene-6,8-dione and its analogues Tsuneo Suzuki, Kiyoshi Tanemura, Chizuko Okada, The Late Kenichi Arai, Akira Awaji, Takahachi Shimizu and Takaaki Horaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2,4-Dihydroxy-6-((R)-4-hydroxy-2-oxopentyl)-3-methylbenzaldehyde C13H16O5 ÏàËÆ¶È:69.2% Archives of Pharmacal Research 2010 33 231-235 Bioactive metabolites from the sponge-derived fungus Aspergillus versicolor Yoon Mi Lee, Huayue Li, Jongki Hong, Hee Young Cho and Kyung Sook Bae, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 2,4-dihydroxy-6-(5-iodo-2-oxopentyl)-3-methylbenzaldehyde C13H15IO4 ÏàËÆ¶È:53.8% Journal of the American Chemical Society 2007 129 9860-9861 Total Synthesis, Stereochemical Reassignment, and Absolute Configuration of Chlorofusin Sang Yeul Lee, Ryan C. Clark, and Dale L. Boger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

4Â¥2013-06-05 19:55:53
yaolan123
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ÐÐÎÞÈË: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-05 21:39:17
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²éѯ½á¹û£º¹²²éµ½122¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . indole-3-acetic acid ÏàËÆ¶È:80% 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 . indole-3-acetic acid ÏàËÆ¶È:77.7% Bioscience, Biotechnology, and Biochemistry 2000 64 187-189 Phytotoxicity of Indole-3-acetic Acid Produced by the Fungus, Pythium aphanidermatum Atsumi SHIMADA, Sumiyo TAKEUCHI, Akira NAKAJIMA, Satoshi TANAKA, Tsuyoshi KAWANO, Yasuo KIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 1-¼×»ù-1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 4 . compound C25H19N3 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 5 . tris(1H-indol-3-yl)methane C25H19N3 ÏàËÆ¶È:66.6% 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 . methyl Indol-3-ylacetate C11H11NO2 ÏàËÆ¶È:63.6% 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 -------------------------------------------------------------------------------- 7 . fellutanine A C22H20N4O2 ÏàËÆ¶È:63.6% Journal of Natural Products 2000 63 698-700 New Diketopiperazine Alkaloids from Penicillium fellutanum Anatoly G. Kozlovsky,Nataliya G. Vinokurova,Vladimir M. Adanin,G¨¹nther Burkhardt,Hans-Martin Dahse, and Udo Gräfe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . indole-3-methylethanoate C11H11O2N ÏàËÆ¶È:63.6% Natural Product Sciences 1997 3 106-107 Isolation and Characterization of Indole-3-methylethanoate from Camellia sinensis (L.) O. Kuntz. and its biological activity Roy, Malabika; Ganguly, S.N. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . corynantheine ÏàËÆ¶È:62.5% 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 Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 6c ÏàËÆ¶È:62.5% Canadian Journal of Chemistry 2007 85 42-46 Copper-mediated N-arylation of electron-deficient pyrroles and indoles Henri Bekolo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . bis(1H-indol-2-yl)selenide C16H12N2Se ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2009 17 1648-1653 Synthesis and biological evaluation of fused thio- and selenopyrans as new indolocarbazole analogues with aryl hydrocarbon receptor affinity Emma Wincent, Hamid Shirani, Jan Bergman, Ulf Rannug, Tomasz Janosik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2-chloro-1-methyl-1H-benzo[d]imidazole ÏàËÆ¶È:62.5% Organic Magnetic Resonance 1982 20 212-216 Investigation of benzimidazoles. III¡ªtransmission of the substituent effects in 2-substituted 1-methylbenzimidazoles studied by 13C nuclear magnetic resonance V. A. Lopyrev, L. I. Larina, T. I. Vakul'skaya, E. F. Shibanova, I. A. Titova, M. G. Voronkov and E. E. Liepin'sh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 6-bromoindolyl-3-acetic acid C10H8BrNO2 ÏàËÆ¶È:60% Journal of Natural Products 1993 Vol 56 1553-1558 Structure and Synthesis of Bromoindoles from the Marine Sponge Pseudosuberites hyalinus Thomas Rasmussen, Jan Jensen, Uffe Anthoni, Carsten Christophersen, Per H. Nielsen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5-bromoindole-3-acetic acid ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung C 2002 57 914-922 Cytotoxic Bromoindole Derivatives and Terpenes from the Philippine Marine Sponge Smenospongia sp. D. Tasdemir, T. S..Bugni, G. C. Mangalindan, G. P.Concepci¨®, M. K. Harper, and C. M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3-indolethanol C10H11NO ÏàËÆ¶È:60% Academic Journal of Second Military Medical University 2008 29 1234-1238 Isolation,identification and biological characterization of secondary metabolites produced by a marine Bacillus subtilis HAN Wen-ju, LU Xiao-ling, XU Qiang-zhi, LIU Xiao-yu, JIAO Bing-hua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 3-(2-Hydroxyethyl)indole C10H11NO ÏàËÆ¶È:60% European Journal of Organic Chemistry 1996 1996 49-53 Antibiotics from Gliding Bacteria, LXXIII Indole and Quinoline Derivatives as Metabolites of Tryptophan in Myxobacteria Bettina Böhlendorf, Norbert Bedorf, Rolf Jansen, Wolfram Trowitzsch-Kienast, Gerhard Höfle, Edgar Forche, Klaus Gerth, Herbert Irschik, Brigitte Kunze and Hans Reichenbach Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Compoud 1 C24H27N5O2 ÏàËÆ¶È:58.3% Tetrahedron Letters 2012 53 1169-1172 Highly selective and sensitive fluorescent chemosensor for Hg2+ in aqueous solution Hsiu-Han Wu,Yao-Lin Sun,Chin-Feng Wan,Shih-Tse Yang,Shau-Jiun Chen,Ching-Han Hu,An-Tai Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . donaxine C11H14N2 ÏàËÆ¶È:55.5% Chemistry of Natural Compounds 1996 32 386-512 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES CHAPTER , continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Suitankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 3-methylindole ÏàËÆ¶È:55.5% Journal of Natural Products 1986 Vol 49 534 3-Dimethyallylindole: an Antibacterial and Antifungal Metabolite from Monodora tenuifolia A. O. Adeoye, B. O. Oguntimein, A. M. Clark, C. D. Hufford Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Tri(1H-indol-3-yl)methane C25H19N3 ÏàËÆ¶È:55.5% Canadian Journal of Chemistry 2009 87 416-421 A catalyst-free protocol for the green and efficient condensation of indoles with aldehydes in ionic liquids Abdolkarim Zare, Abolfath Parhami, Ahmad Reza Moosavi-Zare,Alireza Hasaninejad, Ali Khalafi-Nezhad, and Mohammad Hassan Beyzavi Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-05 19:54:55
wangwang1989
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ÐÐÎÞÈË: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-05 21:39:26
|
1 . indole-3-acetic acid ÏàËÆ¶È:80% 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 . indole-3-acetic acid ÏàËÆ¶È:77.7% Bioscience, Biotechnology, and Biochemistry 2000 64 187-189 Phytotoxicity of Indole-3-acetic Acid Produced by the Fungus, Pythium aphanidermatum Atsumi SHIMADA, Sumiyo TAKEUCHI, Akira NAKAJIMA, Satoshi TANAKA, Tsuyoshi KAWANO, Yasuo KIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-¼×»ù-1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:70% 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 4 . compound C25H19N3 ÏàËÆ¶È:66.6% 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 5 . tris(1H-indol-3-yl)methane C25H19N3 ÏàËÆ¶È:66.6% 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 . methyl Indol-3-ylacetate C11H11NO2 ÏàËÆ¶È:63.6% 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 7 . fellutanine A C22H20N4O2 ÏàËÆ¶È:63.6% Journal of Natural Products 2000 63 698-700 New Diketopiperazine Alkaloids from Penicillium fellutanum Anatoly G. Kozlovsky,Nataliya G. Vinokurova,Vladimir M. Adanin,G¨¹nther Burkhardt,Hans-Martin Dahse, and Udo Gräfe Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . indole-3-methylethanoate C11H11O2N ÏàËÆ¶È:63.6% Natural Product Sciences 1997 3 106-107 Isolation and Characterization of Indole-3-methylethanoate from Camellia sinensis (L.) O. Kuntz. and its biological activity Roy, Malabika; Ganguly, S.N. Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . corynantheine ÏàËÆ¶È:62.5% 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 Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 6c ÏàËÆ¶È:62.5% Canadian Journal of Chemistry 2007 85 42-46 Copper-mediated N-arylation of electron-deficient pyrroles and indoles Henri Bekolo Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . bis(1H-indol-2-yl)selenide C16H12N2Se ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2009 17 1648-1653 Synthesis and biological evaluation of fused thio- and selenopyrans as new indolocarbazole analogues with aryl hydrocarbon receptor affinity Emma Wincent, Hamid Shirani, Jan Bergman, Ulf Rannug, Tomasz Janosik Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-chloro-1-methyl-1H-benzo[d]imidazole ÏàËÆ¶È:62.5% Organic Magnetic Resonance 1982 20 212-216 Investigation of benzimidazoles. III¡ªtransmission of the substituent effects in 2-substituted 1-methylbenzimidazoles studied by 13C nuclear magnetic resonance V. A. Lopyrev, L. I. Larina, T. I. Vakul'skaya, E. F. Shibanova, I. A. Titova, M. G. Voronkov and E. E. Liepin'sh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6-bromoindolyl-3-acetic acid C10H8BrNO2 ÏàËÆ¶È:60% Journal of Natural Products 1993 Vol 56 1553-1558 Structure and Synthesis of Bromoindoles from the Marine Sponge Pseudosuberites hyalinus Thomas Rasmussen, Jan Jensen, Uffe Anthoni, Carsten Christophersen, Per H. Nielsen Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-bromoindole-3-acetic acid ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung C 2002 57 914-922 Cytotoxic Bromoindole Derivatives and Terpenes from the Philippine Marine Sponge Smenospongia sp. D. Tasdemir, T. S..Bugni, G. C. Mangalindan, G. P.Concepci¨®, M. K. Harper, and C. M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-indolethanol C10H11NO ÏàËÆ¶È:60% Academic Journal of Second Military Medical University 2008 29 1234-1238 Isolation,identification and biological characterization of secondary metabolites produced by a marine Bacillus subtilis HAN Wen-ju, LU Xiao-ling, XU Qiang-zhi, LIU Xiao-yu, JIAO Bing-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-(2-Hydroxyethyl)indole C10H11NO ÏàËÆ¶È:60% European Journal of Organic Chemistry 1996 1996 49-53 Antibiotics from Gliding Bacteria, LXXIII Indole and Quinoline Derivatives as Metabolites of Tryptophan in Myxobacteria Bettina Böhlendorf, Norbert Bedorf, Rolf Jansen, Wolfram Trowitzsch-Kienast, Gerhard Höfle, Edgar Forche, Klaus Gerth, Herbert Irschik, Brigitte Kunze and Hans Reichenbach Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Compoud 1 C24H27N5O2 ÏàËÆ¶È:58.3% Tetrahedron Letters 2012 53 1169-1172 Highly selective and sensitive fluorescent chemosensor for Hg2+ in aqueous solution Hsiu-Han Wu,Yao-Lin Sun,Chin-Feng Wan,Shih-Tse Yang,Shau-Jiun Chen,Ching-Han Hu,An-Tai Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . donaxine C11H14N2 ÏàËÆ¶È:55.5% Chemistry of Natural Compounds 1996 32 386-512 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES CHAPTER , continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Suitankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-methylindole ÏàËÆ¶È:55.5% Journal of Natural Products 1986 Vol 49 534 3-Dimethyallylindole: an Antibacterial and Antifungal Metabolite from Monodora tenuifolia A. O. Adeoye, B. O. Oguntimein, A. M. Clark, C. D. Hufford Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Tri(1H-indol-3-yl)methane C25H19N3 ÏàËÆ¶È:55.5% Canadian Journal of Chemistry 2009 87 416-421 A catalyst-free protocol for the green and efficient condensation of indoles with aldehydes in ionic liquids Abdolkarim Zare, Abolfath Parhami, Ahmad Reza Moosavi-Zare,Alireza Hasaninejad, Ali Khalafi-Nezhad, and Mohammad Hassan Beyzavi Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 3d C14H9N3O4 ÏàËÆ¶È:55.5% Heterocycles 2008 76 249-256 Ultrasound-Assisted N-Arylation of Indoles without any Catalyst Hui Xu, Lei Lv, Ling-ling Fan, and Xiao-qiang He Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Â-3-thieno[3,2-b]pyrrolyI-L-alanin ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 1995 5 1133-1134 Robert S. Phillips, Louis A. Cohen, Ulf Annby, David Wensbo, Salo Gronowitz Robert S. Phillips, Louis A. Cohen, Ulf Annby, David Wensbo, Salo Gronowitz Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 3d C14H9N3O4 ÏàËÆ¶È:55.5% Zeitschrift f¨¹r Naturforschung B 2008 63 298-302 Microwave-assisted N-Arylation of Indoles via C(sp2)-N(sp2) Bond Formation by Aromatic Nucleophilic Substitution Reactions H. Xu and L.-L. Fan Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound IV ÏàËÆ¶È:55.5% Russian Journal of Organic Chemistry 2005 41 1516-1521 1H and 13C NMR Study of Bifurcated Intramolecular Hydrogen Bonds in 2,6-Bis(2-pyrrolyl)pyridine and 2,6-Bis(1-vinyl-2-pyrrolyl)pyridine A. V. Afonin, I. A. Ushakov, D. E. Simonenko, E. Yu. Shmidt and N. V. Zorina, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 1-methyl-2-(trifluoromethyl)-1H-benzo[d]imidazole ÏàËÆ¶È:55.5% Organic Magnetic Resonance 1982 20 212-216 Investigation of benzimidazoles. III¡ªtransmission of the substituent effects in 2-substituted 1-methylbenzimidazoles studied by 13C nuclear magnetic resonance V. A. Lopyrev, L. I. Larina, T. I. Vakul'skaya, E. F. Shibanova, I. A. Titova, M. G. Voronkov and E. E. Liepin'sh Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . indole-3-acetic acid ÏàËÆ¶È:55.5% Journal of Agricultural and Food Chemistry 2000 48 4687-4692 Isolation and Characterization of Fungal Inhibitors from Epichloë festucae Qin Yue, Christina J. Miller, James F. White, Jr., and Michael D. Richardson Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Indol-3-ylmethylsulfamide C9H11N3O2S ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2006 14 4958-4979 Toward the control of Leptosphaeria maculans: Design, syntheses, biological activity, and metabolism of potential detoxification inhibitors of the crucifer phytoalexin brassinin M. Soledade C. Pedras, Mukund Jha Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . N-Methyltryptamine ÏàËÆ¶È:54.5% Journal of Natural Products 2011 74 2304-2308 Antifouling Properties of Simple Indole and Purine Alkaloids from the Mediterranean Gorgonian Paramuricea clavata Nicolas P enez, G erald Culioli, Thierry P erez, Jean-Franc-ois Briand, Olivier P. Thomas, and Yves Blache Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3-(5'-indolyl)-2-thioxo-4-imidazolidinone C11H9N3OS ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2003 40 665-670 Synthesis of 3-¦¸-amino-2-thiohydantoins J¨®zef Ryczek Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . N-methyltryptamine ÏàËÆ¶È:54.5% 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 |

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²éѯ½á¹û£º¹²²éµ½3¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2,4-dihydroxy-3-methyl-6-(2-oxopropyl)benzaldehyde C11H12O4 ÏàËÆ¶È:69.2% Journal of Heterocyclic Chemistry 2001 38 1409-1418 Synthesis of 7-acetyloxy-3,7-dimethy1-7,8-dihydro-6H-isochromene-6,8-dione and its analogues Tsuneo Suzuki, Kiyoshi Tanemura, Chizuko Okada, The Late Kenichi Arai, Akira Awaji, Takahachi Shimizu and Takaaki Horaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2,4-Dihydroxy-6-((R)-4-hydroxy-2-oxopentyl)-3-methylbenzaldehyde C13H16O5 ÏàËÆ¶È:69.2% Archives of Pharmacal Research 2010 33 231-235 Bioactive metabolites from the sponge-derived fungus Aspergillus versicolor Yoon Mi Lee, Huayue Li, Jongki Hong, Hee Young Cho and Kyung Sook Bae, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2,4-dihydroxy-6-(5-iodo-2-oxopentyl)-3-methylbenzaldehyde C13H15IO4 ÏàËÆ¶È:53.8% Journal of the American Chemical Society 2007 129 9860-9861 Total Synthesis, Stereochemical Reassignment, and Absolute Configuration of Chlorofusin Sang Yeul Lee, Ryan C. Clark, and Dale L. Boger Structure 13C NMR ̼Æ×Ä£Äâͼ |

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