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namujila: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-13 14:19:02
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namujila: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-13 14:19:02
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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£º¹²²éµ½54¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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