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| CDCl3£º 12.7, 12.9, 15.2, 20.7, 22.8, 23.0, 25.9, 26.9, 27.0, 41.3, 46.2, 59.2, 66.4, 74.8, 76.2, 85.7, 91.1, 111.7, 119.9, 134.8, 139.1, 142.6, 146.8, 163.8, 169.1, 171.5, 209.5 |
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2Â¥2013-09-27 07:52:05
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²éѯ½á¹û£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 11¦Â-hydroxyisoaustinone C25H30O7 ÏàËÆ¶È:66.6% Journal of the American Chemical Society 2012 132 4709-4720 Two Separate Gene Clusters Encode the Biosynthetic Pathway for the Meroterpenoids Austinol and Dehydroaustinol in Aspergillus nidulans Hsien-Chun Lo, Ruth Entwistle, Chun-Jun Guo, Manmeet Ahuja, Edyta Szewczyk, Jui-Hsiang Hung, Yi-Ming Chiang, Berl R. Oakley, and Clay C. C. Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . isoaustinone ÏàËÆ¶È:62.9% Journal of the American Chemical Society 2012 132 4709-4720 Two Separate Gene Clusters Encode the Biosynthetic Pathway for the Meroterpenoids Austinol and Dehydroaustinol in Aspergillus nidulans Hsien-Chun Lo, Ruth Entwistle, Chun-Jun Guo, Manmeet Ahuja, Edyta Szewczyk, Jui-Hsiang Hung, Yi-Ming Chiang, Berl R. Oakley, and Clay C. C. Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . austinolide C25H30O6 ÏàËÆ¶È:59.2% Zeitschrift f¨¹r Naturforschung B 2007 62b 1035-1044 Four Additional Meroterpenes Produced by Penicillium sp Found in Association with Melia azedarach. Possible Biosynthetic Intermediates to Austin Taicia Pacheco Fill, Grace Kelli Pereira, Regina M. Geris dos Santos, and Edson Rodrigues-Fo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . austin ÏàËÆ¶È:59.2% Journal of the Chemical Society, Perkin Transactions 1 1982 2687-2692 Studies on fungal metabolites. Part 3. 13C N.m.r. spectral and structural studies on austin and new related meroterpenoids from Aspergillus ustus, Aspergillus variecolor, and Penicillium diversum Thomas J. Simpson, Desmond J. Stenzel, Alan J. Bartlett, Eugene O'Brien and John S. E. Holker Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . methionine ÏàËÆ¶È:59.2% Journal of the Chemical Society, Perkin Transactions 1 1989 807-816 Studies on the biosynthesis of the mycotoxin austin, a meroterpenoid metabolite of Aspergillus ustus Salman A. Ahmed, Fiona E. Scott, Desmond J. Stenzel, Thomas J. Simpson, Richard N. Moore, Laird A. Trimble, Kunizo Arai and John C. Vederas Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . austin C24H26O8 ÏàËÆ¶È:59.2% Journal of the American Chemical Society 1976 98 6748-6750 Austin, a novel polyisoprenoid mycotoxin from Aspergillus ustus K. K. Chexal, James P. Springer, Jon Clardy, Richard J. Cole, Jerry W. Kirksey, Joe W. Dorner, Horace G. Cutler, Billy J. Strawter Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . austinol C25H30O7 ÏàËÆ¶È:55.5% Journal of the Chemical Society, Perkin Transactions 1 1982 2687-2692 Studies on fungal metabolites. Part 3. 13C N.m.r. spectral and structural studies on austin and new related meroterpenoids from Aspergillus ustus, Aspergillus variecolor, and Penicillium diversum Thomas J. Simpson, Desmond J. Stenzel, Alan J. Bartlett, Eugene O'Brien and John S. E. Holker Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . acetoxydehydroaustin C29H32O11 ÏàËÆ¶È:55.5% Bioscience, Biotechnology, and Biochemistry 1994 58 334-338 Acetoxydehydroaustin, a New Bioactive Compound, and Related Compound Neoaustin from Penicillium sp. MG-11 Hideo Hayashi, Manabu Mukaihara, Sawao Murao, Motoo Arai, Angela Lee Y., Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . austinol C25H30O7 ÏàËÆ¶È:55.5% Bioscience, Biotechnology, and Biochemistry 1994 58 334-338 Acetoxydehydroaustin, a New Bioactive Compound, and Related Compound Neoaustin from Penicillium sp. MG-11 Hideo Hayashi, Manabu Mukaihara, Sawao Murao, Motoo Arai, Angela Lee Y., Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 39 C26H38O6 ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2010 2788-2799 Synthesis of a Novel Taxa-Oxa-Sugar Hybrid Core Structure by Tandem Cross-Enyne Metathesis/IMDA Rahul S. Nandurdikar, Ayyagari V. Subrahmanyam and Krishna P. Kaliappan Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-09-27 13:46:42














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