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WJY515

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WJY515: ½ð±Ò+5 2014-05-04 10:22:38
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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
2Â¥2014-04-30 18:06:32
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