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²éѯ½á¹û£º¹²²éµ½190¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Salicifoliol C13H14O5 ÏàËÆ¶È:92.3% Journal of Natural Products 1989 Vol 52 1139 Salicifoliol, a New Furolactone-Type Lignan from Bupleurum salicifolium Antonio G. Gonz¨¢lez, Rafael Est¨¦vez-Reyes, Carmen Mato Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Salicifoliol C13H14O5 ÏàËÆ¶È:92.3% Journal of Natural Products 1989 Vol 52 1139 Salicifoliol, a New Furolactone-Type Lignan from Bupleurum salicifolium Antonio G. Gonz¨¢lez, Rafael Est¨¦vez-Reyes, Carmen Mato Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Salicifoliol C14H16O6 ÏàËÆ¶È:92.3% Chemistry & Biodiversity 2010 7 2737-2747 Cytotoxic Sesquiterpenes from Magnolia kachirachirai Hsun-Shuo Chang, Shiow-Ju Lee, Cheng-Wei Yang and Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . salicifoliol ÏàËÆ¶È:92.3% Journal of Shenyang Pharmaceutical University 2011 28 420-424 Isolation and identification of the chemical constituents from pine needle of Pinus koraiensis Sieb. et Zucc. L¨¹ Jing, JIA Ling-yun, YUAN Jiu-zhi, ZHANG Jing-jiao, SUN Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (¡À)-salicifoliol C14H14O5 ÏàËÆ¶È:84.6% Canadian Journal of Chemistry 1997 75 840-849 Oxygen insertion in Sesamumindicum furanofuran lignans. Diastereoselective syntheses of enzyme substrate analogues Patrice A. Marchand, Norman G. Lewis, Jaroslav Zajicek Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Salicifoliol ÏàËÆ¶È:84.6% Acta Scientiarum Naturalium Universitatis Sunyatseni 2012 51 63-67 Chemical Constituents of Clematis chinensis Osbeck ZHAO Yang, LIANG Lizhen, LI Houjin, WEN Shiya, LAN Wenjian Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Salicifoliol ÏàËÆ¶È:84.6% Journal of Chinese Pharmaceutical Sciences 2013 22 427-430 Chemical constituents from Qianliang tea Qian Liu, Jun Li, Xingyun Chai, Yong Jiang, Pengfei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . zhebeiresinol ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2010 41 1418-1420 Chemical constituents of Viscum coloratum f. rubroaurantiacum SUN Yong-hui; LING Yong; REN Mei-rong; ZHOU Xue-gang; WANG Jia-yu; MA Ying-li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . zhebeiresinol ÏàËÆ¶È:66.6% Chinese Journal of Natural Medicines 2009 7 28-30 Chemical Constituents of Senecio cannabifolius var. integrilifolius MA Hong-Yan; ; WANG Chang-Hong; YANG Li; ZHANG Mian; WANG Zheng-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . zhebeiresinol ÏàËÆ¶È:66.6% Journal of Integrative Plant Biology 2006 48 236-240 Chemical Constituents of Phacellaria compressa Benth. Xiu-Yun Zhang,, Bo-Gang Li, Min Zhou, Xiao-Hong Yuan, and Guo-Lin Zhang* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . curuilignan ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2013 38 2826-2831 Chemical constituents from stems of Aquilaria sinensis LI Wei, MEI Wen-li, WANG Hao, ZUO Wen-jian, YANG De-lan, DAI Hao-fu, Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (-)-(7R,8'R,8R)-acuminatolide C13H12O5 ÏàËÆ¶È:61.5% Journal of Natural Products 2007 70 39-42 An Efficient and Stereoselective Dearylation of Asarinin and Sesamin Tetrahydrofurofuran Lignans to Acuminatolide by Methyltrioxorhenium/H2O2 and UHP Systems Raffaele Saladino,Cinzia Fiani, Claudia Crestini, Dimitris S. Argyropoulos, Stefano Marini, and Massimiliano Coletta Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (+)-(7S,8R,8'R)-acuminatolide C13H12O5 ÏàËÆ¶È:61.5% Journal of Natural Products 2007 70 39-42 An Efficient and Stereoselective Dearylation of Asarinin and Sesamin Tetrahydrofurofuran Lignans to Acuminatolide by Methyltrioxorhenium/H2O2 and UHP Systems Raffaele Saladino,Cinzia Fiani, Claudia Crestini, Dimitris S. Argyropoulos, Stefano Marini, and Massimiliano Coletta Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . norruspolin 2-(4-hydroxy-3-methoxystyryl)-pyrrolidin C13H17NO2 ÏàËÆ¶È:61.5% Helvetica Chimica Acta 1978 61 1200-1206 Ruspolia hypercrateriformisM.R.: Isolierung und Strukturaufklrung von neuen Pyrrolidin-Alkaloiden. 169. Mitt. ¨¹ber organische Naturstoffe Felix Roessler, Dietmar Ganzinger, Siegfried Johne, Emanuel Schöpp and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (+)-acuminatolide C13H12O5 ÏàËÆ¶È:61.5% Canadian Journal of Chemistry 1997 75 840-849 Oxygen insertion in Sesamumindicum furanofuran lignans. Diastereoselective syntheses of enzyme substrate analogues Patrice A. Marchand, Norman G. Lewis, Jaroslav Zajicek Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . curuilignan D ÏàËÆ¶È:61.5% Journal of Chinese Pharmaceutical Sciences 2012 21 88-92 Chemical constituents from Aquilaria sinensis(Lour.) Gilg Dong Chen; Yue-Lin Song; Chun-Xiao Nie; Xu Ma; Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Marphenol C C13H18O7 ÏàËÆ¶È:61.5% Journal of Natural Products 2013 76 250-255 Dibenzocyclooctadiene Lignans and Norlignans from Fruits of Schisandra wilsoniana Guang-Yu Yang, Rui-Rui Wang, Huai-Xue Mu, Yin-Ke Li, Xiao-Nian Li, Liu-Meng Yang, Yong-Tang Zheng, Wei-Lie Xiao, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . rel-(3R,3'S,4R,4'S)-3,3',4,4'-Tetrahydro-6,6'-dimethoxy[3,3'-bi-2H-benzopyran]-4,4'-diol C20H22O6 ÏàËÆ¶È:58.3% Helvetica Chimica Acta 2000 Vol. 83 3344 Chemical Constituents of Tripterygium wilfordii Guangzhong Yang, Xueqiang Yin, and Yuanchao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . bisbenzopyran C20H22O6 ÏàËÆ¶È:58.3% Planta Medica 1997 63 454-456 A New Bisbenzopyran from Aloe barbadensis Roots Rubeeria Saleem, Shaheen Faizi, Farhat Deeba, Bina Shaheen Siddiqui, and Mahmood Husain Qazi Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (+)-pinoresinol ÏàËÆ¶È:58.3% Chemical & Pharmaceutical Bulletin 1983 31 2993-2997 The Constituents of Eucommia ulmoides OLIV. I. Isolation of (+)-Medioresinol Di-O-¦Â-D-glucopyranoside TAKESHI DEYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (+)-pinoresinol ÏàËÆ¶È:58.3% Chemical & Pharmaceutical Bulletin 1987 35 1785-1789 The Constituents of Eucommia ulmoides OLIV. V. Isolation of Dihydroxydehydrodiconiferyl Alcohol Isomers and Phenolic Compounds TAKESHI DEYAMA,TAKAKO IKAWA,SHIZUKA KITAGAWA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Linchuniinone C12H16O5 ÏàËÆ¶È:58.3% Chinese Chemical Letters 2006 17 1325-1327 Two New Compounds from Lindera chunii Merr Mian ZHANG£¬Chao Feng ZHANG£¬Qi Shi SUN£¬Zheng Tao WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 6-(4-Hydroxy-3-methoxyphenyl)-5,6-dihydropyran-2-one ÏàËÆ¶È:58.3% Molecules 2009 14 2491-2500 Leishmanicidal Activity of Aliphatic and Aromatic Lactones: Correlation Structure-Activity Marcela Castaño, Wilson Cardona, Winston Quiñones, Sara Robledo and Fernando Echeverri Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . d-pinoresinol ÏàËÆ¶È:58.3% Acta Pharmaceutica Sinica 1996 31 524-529 STUDIES ON CHEMICAL CONSTITUENTS OF ROOTS OF EUPHORBIA PEKINENSIS LY Kong and ZD Min Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . pinoresinol C20H22O6 ÏàËÆ¶È:58.3% Natural Product Research 2002 16 359-363 Pinoresinol from Ipomoea Cairica Cell Cultures Csilla P¨¢ska; Gabbriella Innocenti; Mariagrazia Ferlin; M¨®nika Kunv¨¢ri; Mikl¨®s L¨¢szl¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (E)-3,3'-dimethoxy-4,4'-dihydroxystilbene ÏàËÆ¶È:58.3% China Journal of Chinese Materia Medica 2009 34 718-720 Studies on chemical constituents of roots of Linum usita tissimum SUN Jianlong, DENG Anjun, LI Zhihong, QIN Hailin Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . (+)-pinoresinol ÏàËÆ¶È:58.3% China Journal of Chinese Materia Medica 2000 25 541-543 Studies on Chemical Constituents of Ligustrum obtusifolium Sieb. et Zucc. ZHOU Lixin, DING Yi Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 3,4-dimethoxycinnamyl alcohol ÏàËÆ¶È:58.3% Fitoterapia 2003 74 308-311 Antimicrobial and cytotoxic constituents of Loranthus globosus G.Sadik , R.Islam , M.M.Rahman , P.Khondkar,M.A. Rashidc, S.D. Sarker Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . pinoresinol C20H22O6 ÏàËÆ¶È:58.3% Fitoterapia 2003 74 184-187 Bioactive constituents of Leptadenia arborea A.El-Hassan , M.El-Sayed , A.I. Hamed , I.K. Rheeb,A.A. Ahmed, K.P. Zeller, R. Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ |

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