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WJY515: ½ð±Ò+5 2014-05-04 10:22:38
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WJY515: ½ð±Ò+5 2014-05-04 10:22:38
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²éѯ½á¹û£º¹²²éµ½331¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-Acetoxy-2-methyl-5-(1,2,2-trimethylcyclopentyl)phenol C17H24O3 ÏàËÆ¶È:100% Tetrahedron Letters 2005 46 6105-6109 Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 4-Acetoxy-5-methyl-2-(1,2,2-trimethylcyclopentyl)phenyl acetate C19H26O4 ÏàËÆ¶È:73.6% Tetrahedron Letters 2005 46 6105-6109 Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (-)-1-hydroxy-2-methoxyherbertene C16H24O2 ÏàËÆ¶È:70.5% Journal of Natural Medicines 2010 64 417-422 Cytotoxic, radical scavenging and antimicrobial activities of sesquiterpenoids from the Tahitian liverwort Mastigophora diclados (Brid.) Nees (Mastigophoraceae) Ismiarni Komala, Takuya Ito, Fumihiro Nagashima, Yasuyuki Yagi and Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-Acetoxy-5-methyl-2-(1,2,2-trimethylcyclopentyl) phenol C17H24O3 ÏàËÆ¶È:70.5% Tetrahedron Letters 2005 46 6105-6109 Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 1,4-cuparenediol C15H22O2 ÏàËÆ¶È:64.7% Phytochemistry 1997 46 145-150 Sesquiterpenoids from the three Japanese liverworts Lejeunea aquatica, L. flava and L. japonica Masao Yoyota, Hiroki Koyama, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (¡À)-herbertenediol ÏàËÆ¶È:64.7% Tetrahedron Letters 2000 41 7563-7566 New total synthesis of (¡À)-herbertene, (¡À)-¦Â-herbertenol and (¡À)-herbertenediol Pranab Dutta Gupta, Ashutosh Pal, Arnab Roy, Debabrata Mukherjee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,4-cuparenediol ÏàËÆ¶È:64.7% Tetrahedron Letters 2003 44 737-740 Stereoselective total syntheses of (¡À)-1,14-herbertenediol and (¡À)-tochuinyl acetate and facile total syntheses of (¡À)-¦Á-herbertenol, (¡À)-¦Â-herbertenol and (¡À)-1,4-cuparenediol Tapas Paul, Ashutosh Pal, Pranab Dutta Gupta, Debabrata Mukherjee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-Acetyloxy-2-methyl-4-(1,2,2-trimethylcyclopentyl) phenol ÏàËÆ¶È:64.7% Tetrahedron Letters 2005 46 6105-6109 Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 5-Methyl-2-(1,2,2-trimethylcyclopentyl)benzene-1,4-diol ÏàËÆ¶È:64.7% Tetrahedron Letters 2005 46 6105-6109 Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-Methoxy-5-methyl-2-(1,2,2-trimethylcyclopentyl) phenol ÏàËÆ¶È:64.7% Tetrahedron Letters 2005 46 6105-6109 Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . mastigophorene A C30H42O4 ÏàËÆ¶È:64.7% Journal of the Chemical Society, Perkin Transactions 1 1991 2737-2741 Novel neurotrophic isocuparane-type sesquiterpene dimers, mastigophorenes A, B, C and D, isolated from the liverwort Mastigophora diclados Yoshiyasu Fukuyama and Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . mastigophorene B C30H42O4 ÏàËÆ¶È:64.7% Journal of the Chemical Society, Perkin Transactions 1 1991 2737-2741 Novel neurotrophic isocuparane-type sesquiterpene dimers, mastigophorenes A, B, C and D, isolated from the liverwort Mastigophora diclados Yoshiyasu Fukuyama and Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 2-hydroxy-3-(1,2,2-trimethylcyclopentyl)-6-methylphenyl acetate C17H24O3 ÏàËÆ¶È:64.7% Tetrahedron 2006 62 9393-9402 Structure revision of HM-3, an aromatic sesquiterpene isolated from the phytopathogenic fungus Helicobasidium mompa. First total syntheses of HM-3 and HM-4 A. Srikrishna, P.C. Ravikumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 7a ÏàËÆ¶È:63.1% Journal of the Chemical Society, Perkin Transactions 1 1991 2737-2741 Novel neurotrophic isocuparane-type sesquiterpene dimers, mastigophorenes A, B, C and D, isolated from the liverwort Mastigophora diclados Yoshiyasu Fukuyama and Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (-)-aromadendra-1(10),3-diene C15H22 ÏàËÆ¶È:58.8% Phytochemistry 2005 66 599-609 Sesquiterpene constituents from the essential oil of the liverwort Plagiochila asplenioides Adewale Martins Adio, Wilfried A. König Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . lanceoloxide C15H24O ÏàËÆ¶È:58.8% Phytochemistry 2004 65 2045-2049 Sesquiterpenes from the east African sandalwood Osyris tenuifolia Andreas Th. Kreipl, Wilfried A. König Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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