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1 .     evernic acid
    ÏàËÆ¶È:65%
Chinese Pharmaceutical Journal          2009          44          1137-1140
Studies on Chemical Constituents of Acanthopanax brachypus(¢ò)
HU Hao-bin, FAN Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     evernic acid
    ÏàËÆ¶È:60%
Phytochemistry          1998          48          815-822
NMR assignments of depsides and tridepsides of the lichen family umbilicariaceae
Takao Narui, Keiko Sawada, Satoshi Takatsuki, Toru Okuyama, Chicita F. Culberson, William Louis Culberson, Shoji Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     evernine
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          1978          61          2899-2904
Synth¨¨se de l'¨¦vernine
Gilles Nicollier, Michel Rebetez, Raffaele Tabacchi, Hans Gerlach and Adolf Thalmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     it isolecanoric acid
C16H14O7     ÏàËÆ¶È:60%
Bulletin of the Chemical Society of Japan          1987          60          1917-1918
Chemical Studies on the Lichen. I. The Structure of Isolecanoric Acid, a New ortho-Depside Isolated from Parmelia tinctorum Despr.
Atsushi Sakurai, Yohko Goto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Stilbostemin J
C16H18O4     ÏàËÆ¶È:55%
Journal of Asian Natural Products Research          2006          8          47-53
Stilbenoids from Stemona japonica
XIN-ZHOU YANG, CHUN-PING TANG and YANG YE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     methyl evernate
    ÏàËÆ¶È:55%
Phytochemistry          1998          48          815-822
NMR assignments of depsides and tridepsides of the lichen family umbilicariaceae
Takao Narui, Keiko Sawada, Satoshi Takatsuki, Toru Okuyama, Chicita F. Culberson, William Louis Culberson, Shoji Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 3f
C19H21NO2S     ÏàËÆ¶È:55%
Organic letters          2001          3          229-232
An Expedient Route to 2,3-Substituted and Fused Benzo[a]quinolizine-4-thione Framework via Ring Annulation with ¦Â-Oxodithioesters
Amrita Roy, Sukumar Nandi, Hiriyakkanavar Ila, and Hiriyakkanavar Junjappa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ethyl 5,7-dihydroxy-4-oxo-3-phenoxychromene-2-carboxylate
C18H14O7     ÏàËÆ¶È:55%
Journal of the Chemical Society, Perkin Transactions 1          1993                   1153-1159
Phenolic constituents of Glycyrrhiza species. Part 10. Glyasperin E, a new 3-phenoxychromen-4-one derivative from the roots of Glycyrrhiza aspera
Lu Zeng, Toshio Fukai, Taro Nomura, Ru-Yi Zhang and Zhi-Cen Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-(5-fluoro-2-trifluoromethylphenylamino)-2-isopropyl-7H-furo[3,2-g]chromen-7-one
C21H15F4NO3     ÏàËÆ¶È:55%
Russian Journal of Organic Chemistry          2011          47          1390-1403
Plant coumarins: VII. Amination of oreoselone trifluoromethanesulfonate
A. V. Lipeeva, E. E. Shul¡¯ts, M. M. Shakirov and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N-(2-(2,4-Dihydroxyphenyl)-4-oxothiazolidin-3-yl)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)Acetamide
C21H18N2O7S     ÏàËÆ¶È:52.3%
Molecules          2010          15          6795-6809
Synthesis and Antioxidant Activity of Some New Coumarinyl-1,3-Thiazolidine-4-ones
Milan Čačić, Maja Molnar, Bojan Šarkanj, Elizabeta Has-Schön and Valentina Rajković
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     micromarin-A
C20H22O6     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2000          48(3)          334-338
Chemical Constituents of Micromelum minutum. Isolation and Structural Elucidation of New Coumarins
Chihiro ITO,Takashi OTSUKA,Nijsiri RUANGRUNGSI,and Hiroshi FURUKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     angelol H
C20H26O7     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1982          30          2025-2035
Studies on Coumarins from the Root of Angelica pubescens MAXIM. IV. Structures of Angelol-Type Prenylcoumarins
KIMIYE BABA,YOUKO MATSUYAMA and MITSUGI KOZAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-(5-Ethoxycarbonyl-2-furyl)-4-hydroxy-7-methoxy-6-propylcoumari
    ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1998          34          32-37
SYNTHESIS AND SPECTRAL PROPERTIES OF 3-FURYL-4-HYDROXYCOUMARINS
V. P. Khilya, a S. V. Kovalev, b N. S. Miroshnichenko, aand A. V. Turov a
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3-formyl-2,4-dihydroxy-6-methylbenzoic acid 3-hydroxy-4-(methoxycarbonyl)-2,5-di-methylphenyl ether
    ÏàËÆ¶È:50%
Fitoterapia          2001          72          565-567
Antifungal constituent from Gordonia dassanayakei
P.S. Athukoralage, H.M.T.B. Herath,S.A. Deraniyagala, R.L.C ijesundera,P.A. Weerasinghe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     1-O-methyl-5-(2-acetoxytridecyl)resorcinol
    ÏàËÆ¶È:50%
Phytochemistry          1997          44          1559-1563
5-alkylresorcinols from Ononis natrix
Librada M. Cañedo, Jose M. Miguel del Corral, Arturo san Feliciano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     5-chloroatranorin
    ÏàËÆ¶È:50%
Journal of Natural Products          1985          Vol 48          157-158
Methyl ¦Â-Orcinolcarboxylate and Depsides from Parmelia furfuracea
S. Caccamese, R. M. Toscano, F. Bellesia, A. Pinetti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 7a
C18H22N2O2     ÏàËÆ¶È:50%
Planta Medica          1996          62          42-45
Total Syntheses of 10-Methoxydihydrocorynantheol and 10-Methoxycorynantheidol
Miettinen, J.; Jokela, R.; Lounasmaa, M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 7b
C18H22N2O2     ÏàËÆ¶È:50%
Planta Medica          1996          62          42-45
Total Syntheses of 10-Methoxydihydrocorynantheol and 10-Methoxycorynantheidol
Miettinen, J.; Jokela, R.; Lounasmaa, M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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