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zemezh: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-28 23:03:48
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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%) ²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . rhodomyrtosone B C26H34O6 ÏàËÆ¶È:84.6% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Rhodomyrtosone B C26H34O6 ÏàËÆ¶È:76.9% Tetrahedron 2008 64 11193-11197 New acylphloroglucinols from the leaves of Rhodomyrtus tomentosa Asadhawut Hiranrat, Wilawan Mahabusarakam Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . rhodomyrtone C26H34O6 ÏàËÆ¶È:69.2% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . rhodomyrtone C26H34O6 ÏàËÆ¶È:68% Australian Journal of Chemistry 2002 55 229-232 Rhodomyrtone, an antibotic from Rhodomyrtus tomentosa Dachriyanus Salni, M. V. Sargent , B. W. Skelton, I. Soediro, M. Sutisna, A. H. White and E. Yulinah Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 6,8-dihydroxy-9-isobutyl-2,2,4,4-tetramethyl-4,9-dihydro-1H-xanthene-1,3(2H)-dione C21H26O5 ÏàËÆ¶È:64% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound (+)-2 C24H30O6 ÏàËÆ¶È:64% European Journal of Organic Chemistry 2013 4078-4084 Enantioselective Synthesis of Myrtucommulone A Maël Charpentier, Marcus Hans and Johann Jauch Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,3-Dioxo-4,9-dihydro-8-hydroxy-6-mthoxy-2,2,4,4-tetramethyl-5-(3-methyl-1-oxobutyl)-9-(2-mthyl-propyl)-1H-xanthene C27H36O6 ÏàËÆ¶È:62.9% Journal of Natural Products 1992 Vol 55 43 Antiviral Phloroglucinols from New Zealand Kunzea Species Stephen J. Bloor Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Kunzeanone A C31H34O6 ÏàËÆ¶È:58.6% Tetrahedron 2004 60 9971-9976 Kunzeanones A, B, and C: novel alkylated phloroglucinol metabolites from Kunzea ambigua Hideyuki Ito, Hitomi Iwamori, Naoki Kasajima, Miyuki Kaneda, Takashi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Kunzeanone B C31H34O6 ÏàËÆ¶È:57.1% Tetrahedron 2004 60 9971-9976 Kunzeanones A, B, and C: novel alkylated phloroglucinol metabolites from Kunzea ambigua Hideyuki Ito, Hitomi Iwamori, Naoki Kasajima, Miyuki Kaneda, Takashi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . myrtucommulone M C49H60O12 ÏàËÆ¶È:56% Organic Letters 2013 15 1862-1865 New Inhibitors of ROS Generation and T-Cell Proliferation from Myrtus communis M. Iqbal Choudhary, Noureen Khan, Manzoor Ahmad, Sammer Yousuf, Hoong-Kun Fun, Samreen Soomro, M. Asif, M. Ahmed Mesaik, and Farzana Shaheen Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ericifolione C30H44O6 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 1423-1424 A New Insecticidal Pyranocyclohexenedione from Kunzea ericifolia Bhupinder P. S. Khambay, David G. Beddie, Monique S. J. Simmonds, and Paul W. C. Green Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . callistenone A C25H32O6 ÏàËÆ¶È:52% Tetrahedron 2013 69 6070-6075 Acylphloroglucinols from Callistemon lanceolatus DC. Suthida Rattanaburi, Wilawan Mahabusarakam, Souwalak Phongpaichit, Anthony R. Carroll Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . callistenone B C25H32O6 ÏàËÆ¶È:52% Tetrahedron 2013 69 6070-6075 Acylphloroglucinols from Callistemon lanceolatus DC. Suthida Rattanaburi, Wilawan Mahabusarakam, Souwalak Phongpaichit, Anthony R. Carroll Structure 13C NMR ̼Æ×Ä£Äâͼ |

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