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thb237: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-21 13:52:18
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thb237: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-21 13:52:18
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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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½5¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-methylfuran-2(5H)-one ÏàËÆ¶È:100% Tetrahedron 2003 59 3237-3251 Bioactive butenolides from Streptomyces antibioticus T¨¹ 99: absolute configurations and synthesis of analogs Gilles Grossmann, Marc Poncioni, Marc Bornand, Benoı̂t Jolivet, Markus Neuburger, Urs S¨¦quin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . penangin ÏàËÆ¶È:60% Phytochemistry 1993 32 933-936 Different types of sulphur-containing amides from Glycosmis cf. chlorosperma Harald Greger, Franz Hadacek, Otmar Hofer, Gerald Wurz, Gabriela Zechner Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Ethyl 3,3,3-[2H,2H,2H]-methyl [4,4,4-2H,2H,2H]-but-2-eneoate ÏàËÆ¶È:60% Organic & Biomolecular Chemistry 2008 6 2346-2354 Stereochemistry of eudesmane cation formation during catalysis by aristolochene synthase from Penicillium roqueforti David J. Miller, Jiali Gao, Donald G. Truhlar, Neil J. Young, Veronica Gonzalez and Rudolf K. Allemann Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . penangin ÏàËÆ¶È:60% Tetrahedron 1994 50 6279-6286 Synthesis and corrected structures of sulphur-containing amides from Glycosmis species: Sinharines, penimides, and illukumbins Sabine Hinterberger, Otmar Hofer, Harald Greger Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2¦Á-methyl-9,20-di-O-tert-butyldimethylsilyl-2',4',4'-tri-O-triethylsilyldesmycosin-3,20-acetal ÏàËÆ¶È:60% The Journal of Antibiotics 2006 59 98-104 Synthesis of 2-Methyl 16-Membered Macrolide Derived from Tylosin FREE Yuichi Terui, Kenji Kinoshita, Yoshie Kaneda, Toshi Akashi, Takuya Hamaguchi and Akira Kawashima Structure 13C NMR ̼Æ×Ä£Äâͼ Copyright © 2009-2011 ÉϺ£Î¢Æ×ÐÅÏ¢¼¼ÊõÓÐÏÞ¹«Ë¾ Shanghai Micronmr Infor Technology Co., Ltd., All Rights Reserved |
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