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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£º¹²²éµ½21¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . rhodomyrtone C26H34O6 ÏàËÆ¶È:100% 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 2 . rhodomyrtone C26H34O6 ÏàËÆ¶È:96.1% 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 3 . Rhodomyrtosone B C26H34O6 ÏàËÆ¶È:73.0% Tetrahedron 2008 64 11193-11197 New acylphloroglucinols from the leaves of Rhodomyrtus tomentosa Asadhawut Hiranrat, Wilawan Mahabusarakam Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . rhodomyrtosone B C26H34O6 ÏàËÆ¶È:73.0% 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 5 . callistenone A C25H32O6 ÏàËÆ¶È:72% 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 6 . 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:70.3% Journal of Natural Products 1992 Vol 55 43 Antiviral Phloroglucinols from New Zealand Kunzea Species Stephen J. Bloor Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . rhodomyrtosone E C30H34O6 ÏàËÆ¶È:70% Bioorganic & Medicinal Chemistry Letters 2014 24 3096-3099 Chemical constituents from Eucalyptus citriodora Hook leaves and their glucose transporter 4 translocation activities Chao Wang, Jing Yang, Ping Zhao, Qi Zhou, Zhinan Mei, Guangzhong Yang, Xinzhou Yang, Yunjiang Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6,8-dihydroxy-9-isobutyl-2,2,4,4-tetramethyl-4,9-dihydro-1H-xanthene-1,3(2H)-dione C21H26O5 ÏàËÆ¶È:60% 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 9 . 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 10 . 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 11 . 5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chro-men-4-one C26H26O7 ÏàËÆ¶È:56% Tetrahedron 2013 69 5850-5858 Total syntheses of norartocarpin and artocarpin Wen-Jing Zhang, Jing-Fang Wu, Peng-Fei Zhou, Yang Wang, Ai-Jun Hou Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . callistenone C C25H34O7 ÏàËÆ¶È:56% 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 . leucyl-N-methyl-leucyl-leucyl-N-methyl-leucine C26H50N4O5 ÏàËÆ¶È:53.8% Chinese Journal of Organic Chemistry 2012 32 727-731 Isolation and Identification of Two New Compounds Linear Tetrapeptide and Monohydroxysteroid Wang; Changjun Liang; Yuanwei Liao; Xiaojian Xu; Shihai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . isomyrtucommulone B ÏàËÆ¶È:52% Journal of Natural Products 2002 65 334-338 Oligomeric Acylphloroglucinols from Myrtle (Myrtus communis) Giovanni Appendino,Federica Bianchi, Alberto Minassi, Olov Sterner, Mauro Ballero, and Simon Gibbons Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3,4-Dihydro-5,7-dihydroxy-3',3'-dimethyl-6,8-Di-(3-methyl-butanoyl)-spiro-2H-1-benzopyran-2,2'-bicyclo-[2.2.1]heptane C27H38O5 ÏàËÆ¶È:52% Bioorganic & Medicinal Chemistry 2008 16 1328-1336 S-Euglobals: Biomimetic synthesis, antileishmanial, antimalarial, and antimicrobial activities Sandip B. Bharate, Shabana I. Khan, Babu L. Tekwani, Melissa Jacob, Ikhlas A. Khan, Inder Pal Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 6 ÏàËÆ¶È:52% Tetrahedron 2003 59 7131-7133 Isolation, characterisation and synthesis of an insecticidal tetramethyltetrahydrochromenedione-spiro-bicyclo[3.1.1]cycloheptane from two species of Myrtaceae Bhupinder P.S Khambay, David G Beddie, Antony M Hooper, Monique S.J Simmonds Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . rhodomyrtosone I C28H30O6 ÏàËÆ¶È:52% Natural Product Research 2012 26 1904¨C1909 A new flavellagic acid derivative and phloroglucinol from Rhodomyrtus tomentosa A. Hiranrat, W. Chitbankluoi, W. Mahabusarakam, S. Limsuwan & S.P. Voravuthikunchai Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 42,43 C22H48N4 ÏàËÆ¶È:52% The Journal of Organic Chemistry 2002 67 245-258 Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis David E. Williams, Kyle S. Craig, Brian Patrick, Lianne M. McHardy, Rob van Soest, Michel Roberge, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 4-cyclohexene-1,3-dioxo-5-hydroxy-2,2,6,6-tetramethyl-4-{1-[2,6-dihydroxy-4-methoxy-3-(3-methyl-l-oxo-butyl)phenyl]-3-methylbutyl} C27H38O7 ÏàËÆ¶È:51.8% Journal of Natural Products 1992 Vol 55 43 Antiviral Phloroglucinols from New Zealand Kunzea Species Stephen J. Bloor Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ericifolione C30H44O6 ÏàËÆ¶È:50% 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 21 . preaustinoid A3 ÏàËÆ¶È:50% 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 |

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