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ÏàËÆ¶È´óÓÚ65%µÄÓÐ 1 . nemerosin ÏàËÆ¶È:77.2% Phytochemistry 2003 1375-1379 Immunosuppressive flavones and lignans from Bupleurum scorzonerifolium Wen-Liang Chang, Li-Wen Chiu, Jenn-Haung Lai, Hang-Ching Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . nemerosin C22H23O7 ÏàËÆ¶È:77.2% Chemical & Pharmaceutical Bulletin 1998 46 871-874 Antiproliferative Constituents in Umbelliferae Plants. III. Constituents in the Root and the Ground Part of Anthriscus sylvestris HOFFM. Ryuji IKEDA,Tsuneatsu NAGAO,Hikaru OKABE,Yukitaka NAKANO,Hisashi MATSUNAGA,Mitsuo KATANO and Masato MORI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . nemerosin ÏàËÆ¶È:77.2% Phytochemistry 1989 28 2863-2866 Lignans from Juniperus thurifera Arturo San Feliciano,Manuel Medarde,Jose L. Lopez,Pilar Puebla,Jose M. Miguel del Corral,Alejandro F. Barrer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . nemerosin ÏàËÆ¶È:77.2% Biological and Pharmaceutical Bulletin 2007 30 1340-1343 Lignans and Coumarins from the Roots of Anthriscus sylvestris and Their Increase of Caspase-3 Activity in HL-60 Cells Gil-Saeng Jeong, Ok-Kyoung Kwon, Bo-Young Park, Sei-Ryang Oh, Kyung-Seop Ahn, Min-Jung Chang, Won Keun Oh, Jin-Cheol Kim, Byung-Sun Min, Youn-Chul Kim, Hyeong-Kyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . gossypifan ÏàËÆ¶È:68.4% Phytochemistry 1995 40 931-932 Gossypifan, a lignan from Jatropha gossypifolia, Biswanath Das, Ratna Das (n¨¦e Chakrabarti) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . isoguamarol C20H18O6 ÏàËÆ¶È:65% Helvetica Chimica Acta 2007 Vol. 90 738 New Lignans from the Roots of Taiwania cryptomerioides Hayata Chiou-Fung Chyu and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . kaerophyllin C21H20O6 ÏàËÆ¶È:65% Planta Medica 1981 43 378-380 Kaerophyllin, A New Lignan from Chaerophyllum maculatum G. A. Mikaya, O. G. Turabelidze, E. P. Kemertelidze and N. S. Wulfson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 4'-O-Demethylsuchilactone ÏàËÆ¶È:65% Phytochemistry 1995 38 715-717 Lignans, biflavones and taxoids from Himalayan Taxus baccata, B. Das, S. Padma Rao, K. V. N. S. Srinivas, J. S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (7E)-4',5-dihydroxy-3,3',5-trimethoxylign-7-en-9,9'-olide C21H22O7 ÏàËÆ¶È:65% Phytochemistry 1990 29 3048-3049 Lignans from wood of Calocedrus formosana Jim-Min Fang,Ming-Ying Liu,Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ |

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1 . nemerosin ÏàËÆ¶È:77.2% Phytochemistry 2003 1375-1379 Immunosuppressive flavones and lignans from Bupleurum scorzonerifolium Wen-Liang Chang, Li-Wen Chiu, Jenn-Haung Lai, Hang-Ching Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . nemerosin C22H23O7 ÏàËÆ¶È:77.2% Chemical & Pharmaceutical Bulletin 1998 46 871-874 Antiproliferative Constituents in Umbelliferae Plants. III. Constituents in the Root and the Ground Part of Anthriscus sylvestris HOFFM. Ryuji IKEDA,Tsuneatsu NAGAO,Hikaru OKABE,Yukitaka NAKANO,Hisashi MATSUNAGA,Mitsuo KATANO and Masato MORI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . nemerosin ÏàËÆ¶È:77.2% Phytochemistry 1989 28 2863-2866 Lignans from Juniperus thurifera Arturo San Feliciano,Manuel Medarde,Jose L. Lopez,Pilar Puebla,Jose M. Miguel del Corral,Alejandro F. Barrer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . nemerosin ÏàËÆ¶È:77.2% Biological and Pharmaceutical Bulletin 2007 30 1340-1343 Lignans and Coumarins from the Roots of Anthriscus sylvestris and Their Increase of Caspase-3 Activity in HL-60 Cells Gil-Saeng Jeong, Ok-Kyoung Kwon, Bo-Young Park, Sei-Ryang Oh, Kyung-Seop Ahn, Min-Jung Chang, Won Keun Oh, Jin-Cheol Kim, Byung-Sun Min, Youn-Chul Kim, Hyeong-Kyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . gossypifan ÏàËÆ¶È:68.4% Phytochemistry 1995 40 931-932 Gossypifan, a lignan from Jatropha gossypifolia, Biswanath Das, Ratna Das (n¨¦e Chakrabarti) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . isoguamarol C20H18O6 ÏàËÆ¶È:65% Helvetica Chimica Acta 2007 Vol. 90 738 New Lignans from the Roots of Taiwania cryptomerioides Hayata Chiou-Fung Chyu and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . kaerophyllin C21H20O6 ÏàËÆ¶È:65% Planta Medica 1981 43 378-380 Kaerophyllin, A New Lignan from Chaerophyllum maculatum G. A. Mikaya, O. G. Turabelidze, E. P. Kemertelidze and N. S. Wulfson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 4'-O-Demethylsuchilactone ÏàËÆ¶È:65% Phytochemistry 1995 38 715-717 Lignans, biflavones and taxoids from Himalayan Taxus baccata, B. Das, S. Padma Rao, K. V. N. S. Srinivas, J. S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (7E)-4',5-dihydroxy-3,3',5-trimethoxylign-7-en-9,9'-olide C21H22O7 ÏàËÆ¶È:65% Phytochemistry 1990 29 3048-3049 Lignans from wood of Calocedrus formosana Jim-Min Fang,Ming-Ying Liu,Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . kaerophyllin C21H20O6 ÏàËÆ¶È:61.9% Journal of Natural Products 1993 Vol 56 318 X-Ray Crystal Structure and Absolute Configuration of Kaerophyllin (Chaerophyllin) Khadga S. Khetwal, Subodh Harbola, Ping Cai, John K. Snyder, M. Gary Newton, S. William Pelletier, Balawant S. Joshi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Suchilactone ÏàËÆ¶È:61.9% Phytochemistry 1995 38 715-717 Lignans, biflavones and taxoids from Himalayan Taxus baccata, B. Das, S. Padma Rao, K. V. N. S. Srinivas, J. S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . kaerophyllin C21H20O6 ÏàËÆ¶È:61.9% Phytochemistry 1990 29 675-678 Isokaerophyllin,a butyrolactone from Bupleurum salicifolium Antonio G. Gonz¨¢lez,Rafael Est¨¦vez-Reyes,Carmen Mato,Ana Ma Est¨¦vez-Braun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . ¦Á-methylclusin (8R, 8'R, 9S) -9¦Á-methoxy-3,4,5-trimethoxy-3',4'-methylenedioxy-8.8'.9.O.9' lignan-¦¤:1,3,5, 1',3',5' C23H28O7 ÏàËÆ¶È:60% Phytochemistry 2000 55 809-813 Analgesic activity of the lignans from Lychnophora ericoides M¨¢rcio L.C. Borsato, Cristiane F.F. Grael, Gl¨®ria E.P.Souza, Norberto P. Lopes Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . jatrophan ÏàËÆ¶È:60% Phytochemistry 1984 23 2323-2327 Gadain, a lignan from jatropha gossypifolia J. Banerji, B. Das, A. Chatterjee, J.N. Shoolery Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . savinin C20H126O6 ÏàËÆ¶È:60% Archives of Pharmacal Research 2005 28 186-189 Anti-estrogenic activity of lignans from Acanthopanax chiisanensis root Sanghyun Lee, Hye Hyun Yoo, Xiang Lan Piao, Ju Sun Kim and Sam Sik Kang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . savinin ÏàËÆ¶È:60% Archives of Pharmacal Research 2011 34 2043-2049 A new lignan glycoside from Juniperus rigida Kyeong Wan Woo, Sang Un Choi, Jong Cheol Park and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . savinin C20H16O6 ÏàËÆ¶È:60% Phytotherapy Research 2005 19 103-106 Lignans from Acanthopanax chiisanensis having an inhibitory activity on prostaglandin E2 production Sanghyun Lee, Hyun Seung Ban, Yong Pil Kim, Bak-Kwang Kim, Seon Haeng Cho, Kazuo Ohuchi and Kuk Hyun Shin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (+)-norchelidonine C19H17NO5 ÏàËÆ¶È:57.8% Planta Medica 1992 58 477 (+)-Norchelidonine from Chelidonium majus Gälden Kadan, Tekant Gözler', and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (-)-yatein C22H24O7 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1987 35 4162-4168 Studies on the Constituents of the Seeds of Hernandia ovigera L. VI. Isolation and Structural Determination of Three Lignans MARIKO TANOGUCHI,MASAO ARIMOTO,HIDEYUKI SAIKA and HIDEO YAMAGUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . cristanine B C18H21NO5 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 2010 58 1119-1122 Structures of New Erythrinan Alkaloids and Nitric Oxide Production Inhibitors from Erythrina crista-galli Masaaki Ozawa, Shunsuke Kawamata, Tadahiro Etoh, Masahiko Hayashi, Kanki Komiyama, Akio Kishida, Chiaki Kuroda and Ayumi Ohsaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . (7E)-4,4'-dihydroxy-3,3',5-trimethoxylign-7-en-9,9'-olide C21H22O7 ÏàËÆ¶È:57.8% Phytochemistry 1990 29 3048-3049 Lignans from wood of Calocedrus formosana Jim-Min Fang,Ming-Ying Liu,Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (3aR,4aS,5R,12R,12aR,13R,13aS)-2,2-dimethyl-3a,4,4a,6,12,12a,13,13a-octahydro-5,12-methano[1,3]dioxolo[4',5':4,5]benzo[1,2-b][1,3]dioxolo[4',5':4,5]benzo[1,2-e]azepin-13-ol C19H23NO5 ÏàËÆ¶È:57.8% European Journal of Organic Chemistry 2011 4571-4587 One-Step Stereospecific Strategy for the Construction of the Core Structure of the 5,11-Methanomorphanthridine Alkaloids in Racemic as well as in Optically Pure Form: Synthesis of (¡À)-Pancracine and (¡À)-Brunsvigine Ganesh Pandey, Ravindra Kumar, Prabal Banerjee and Vedavati G. Puranik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 7¦Á-chloro-7-deoxyepipodophyllotoxin ÏàËÆ¶È:57.1% Journal of Natural Products 1995 Vol 58 870-877 Methyl Ethers of Podophyllotoxin-Related Cyclolignans J. M. Miguel del Corral, M. Gordaliza, M. A. Castro, L. J. Morales, J. L. Lopez, A. San Feliciano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 7-bromo-7-deoxypodophyllotoxin ÏàËÆ¶È:57.1% Journal of Natural Products 1995 Vol 58 870-877 Methyl Ethers of Podophyllotoxin-Related Cyclolignans J. M. Miguel del Corral, M. Gordaliza, M. A. Castro, L. J. Morales, J. L. Lopez, A. San Feliciano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . acutissimalignan B C20H20O6 ÏàËÆ¶È:55% Journal of Natural Products 2008 71(4) 655-663 Dichapetalin-Type Triterpenoids and Lignans from the Aerial Parts of Phyllanthus acutissima Patoomratana Tuchinda, Jittra Kornsakulkarn, Manat Pohmakotr, Palangpon Kongsaeree, Samran Prabpai, Chalobon Yoosook, Jitra Kasisit, Chanita Napaswad, Samaisukh Sophasan, and Vichai Reutrakul Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . guamarol C20H18O6 ÏàËÆ¶È:55% Phytochemistry 1992 31 2841-2845 Lignanolides from bupleurum salicifolium R. Est¨¦vez-Reyes, A. Est¨¦vez-Braun, Antonio G. Gonzalez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 14-Epichelidonine ÏàËÆ¶È:55% Phytochemistry 1991 30 2071-2074 Alkaloids from Sarcocapnos saetabensis Olga Blanco, Luis Castedo, Diego Cortes, M. Carmen Villaverde Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 1-oxohinokinin C20H16O7 ÏàËÆ¶È:55% Phytochemistry 1990 29 3048-3049 Lignans from wood of Calocedrus formosana Jim-Min Fang,Ming-Ying Liu,Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . compound 38 C20H18BrNO6 ÏàËÆ¶È:55% Heterocycles 2008 76 521-539 Total Synthesis of Isoindolobenzazepine Alkaloids, Lennoxamine and Chilenine, Based on Palladium-Catalyzed Reduction of Alkenyl Phosphates Haruhiko Fuwa and Makoto Sasaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . isochaihulactone C22H22O7 ÏàËÆ¶È:54.5% Phytochemistry 2003 1375-1379 Immunosuppressive flavones and lignans from Bupleurum scorzonerifolium Wen-Liang Chang, Li-Wen Chiu, Jenn-Haung Lai, Hang-Ching Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . chaihunaphthone C22H18O7 ÏàËÆ¶È:54.5% Phytochemistry 2003 1375-1379 Immunosuppressive flavones and lignans from Bupleurum scorzonerifolium Wen-Liang Chang, Li-Wen Chiu, Jenn-Haung Lai, Hang-Ching Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . compound 6 ÏàËÆ¶È:54.5% Phytochemistry 1992 31 267-270 Lignans from polar extracts ofJuniperus thurifera Arturo San Feliciano, Jose M. Miguel Del Corral, Jose L. Lopez, Beatriz De Pascual-Teresa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . r-1-phenyl-t-2-carboxy-c-3-(3,4-methylenedioxyphenyl)-5,6-dimethoxyindane C25H22O6 ÏàËÆ¶È:54.5% Tetrahedron 2012 68 913-921 Scope of the formal [3+2] cycloaddition for the synthesis of five-membered ring of functionalized indanes Beatriz Lantaño, Jose Manuel Aguirre, Esteban Ariel Ugliarolo, Rosario Torviso, Nicol¨¢s Pomilio, Graciela Yolanda Moltrasio Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . sylvestrin C22H18O7 ÏàËÆ¶È:54.5% Biological and Pharmaceutical Bulletin 2007 30 1340-1343 Lignans and Coumarins from the Roots of Anthriscus sylvestris and Their Increase of Caspase-3 Activity in HL-60 Cells Gil-Saeng Jeong, Ok-Kyoung Kwon, Bo-Young Park, Sei-Ryang Oh, Kyung-Seop Ahn, Min-Jung Chang, Won Keun Oh, Jin-Cheol Kim, Byung-Sun Min, Youn-Chul Kim, Hyeong-Kyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . ¦Â-apopicropodophyllin C22H20O7 ÏàËÆ¶È:52.6% Phytochemistry 2006 67 1224-1231 Structure¨Cactivity relationship of chemical defenses from the freshwater plant Micranthemum umbrosum Amy L. Lane, Julia Kubanek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . threo-austrobailignan-5 C20H22O4 ÏàËÆ¶È:52.6% Planta Medica 2001 67 700-704 Antiproliferative, Anti-Aromatase, Anti-17b-HSD and Antioxidant Activities of Lignans Isolated from Myristica argentea F. Filleur, J. C. Le Bail, J. L. Duroux, A. Simon, A. J. Chulia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . 6-bromo-1-(tert-butyldimethylsilyl)-3-[1-hydroxy-1(3,4-methylenedioxyphenyl)methyl]indole C22H26BrNO3Si ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1996 44 1831-1839 Total Synthesis of Nortopsentins A-D, Marine Alkaloids Ikuo KAWASAKI,Masayuki YAMASHITA and Shunsaku OHTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . savinin ÏàËÆ¶È:52.6% Journal of Natural Products 1984 Vol 47 331-341 Studies on Aristolochia III. Isolation and Biological Evaluation of Constituents of Aristolochia indica Roots for Fertility-Regulating Activity Chun-Tao Che, Mohamed S. Ahmed, Sam S. Kang, Donald P. Waller, A. S. Bingel, Annamarie Martin, Pathmanayaki Rajamahendran, Nuntavan Bunyapraphatsara, David C. Lankin, Geoffrey A. Cordell, Djaja D. Soejarto, R. O. B. Wijesekera, Harry H. S. Fong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . 1-O-acetyllycorine ÏàËÆ¶È:52.6% Journal of Natural Products 1986 Vol 49 90 Isolation and Structural Characterization of Lutessine, a New Alkaloid from Bulbs of Sternbergia lutea A. Evidente Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . deoxypodorhizon C22H24O7 ÏàËÆ¶È:52.6% Journal of Natural Products 1992 Vol 55 184 The Role of Dianion Coupling in the Synthesis of Dibenzylbutane Lignans John L. Belletire, Douglas F. Fry, Susan L. Fremont Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . isodeoxypodophyllotoxin ÏàËÆ¶È:52.6% Journal of Natural Products 1993 Vol 56 1728 Cytotoxic Constituents from Hyptis verticillata Miriam Novelo, Jos¨¦ G. Cruz, Lourdes Hern¨¢ndez, Rogelio Pereda-Miranda, Heebyung Chai, Woongchon Mar, John M. Pezzuto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . N-(2-chloro-4,5-methylenedioxybenzyl)-3-benzyloxyaniline C21H18ClNO3 ÏàËÆ¶È:52.6% Phytochemistry 1996 41 323-326 Alkaloids from Crinum firmifolium var. hygrophilum Judith Razafimbelo, Marta Andriantsiferana, Genevieve Baudouin, François Tillequin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . (-)-4'-O-Demethylyatein C21H22O7 ÏàËÆ¶È:52.6% Phytochemistry 1994 37 1699-1702 4-O-Demethylyatein from the branch wood ofThuja occidentalis Shingo Kawai, Takao Hasegawa, Maiko Gotoh, Hideo Ohashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . (7E,8'R)-7,8-Didehydroarctigenin ÏàËÆ¶È:52.6% Phytochemistry 1994 37 1101-1107 Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species J.Alberto Marco, Juan F. Sanz-Cervera, Vicente Garcia-Lliso, Alfonso Susanna, Nuria Garcia-Jacas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . methyl 3-(2-piperonylphenyl)-2-diazo-3-oxopropanoate C18H14N2O5 ÏàËÆ¶È:52.6% Heterocycles 2006 70 635-646 Enantioselective Synthesis of 3-Arylindan-1-ones via Intramolecular C-H Insertion Reactions of ¦Á-Diazo-¦Â-Ketoesters Catalyzed by Chiral Dirhodium(II) Carboxylates Yoshihiro Natori, Masahiro Anada, Seiichi Nakamura, Hisanori Nambu, and Shunichi Hashimoto* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . 14-(Benzo[d][1,3]dioxol-5-yl)-14H-dibenzo[a,j]xanthene C28H18O3 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry Letters 2009 19 5590-5593 Synthesis and in vitro study of 14-aryl-14H-dibenzo[a.j]xanthenes as cytotoxic agents Asish K. Bhattacharya, Kalpeshkumar C. Rana, Mohammad Mujahid, Irum Sehar, Ajit K. Saxena Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . N-(4-(Benzo[d][1,3]dioxol-5-yl)butan-2-yl)-3-methoxyaniline C18H21NO3 ÏàËÆ¶È:52.6% Molecules 2010 15 2453-2472 Bifunctional Catalysis: Direct Reductive Amination of Aliphatic Ketones with an Iridium-Phosphate Catalyst Barbara Villa-Marcos, Chaoqun Li, Keith R. Mulholland, Philip J. Hogan and Jianliang Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . helioxanthin C20H12O6 ÏàËÆ¶È:52.6% Archives of Pharmacal Research 2005 28 186-189 Anti-estrogenic activity of lignans from Acanthopanax chiisanensis root Sanghyun Lee, Hye Hyun Yoo, Xiang Lan Piao, Ju Sun Kim and Sam Sik Kang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . Spiro{2,5-dihydro-3-dimethylamino-furan-2,8'-4',4'a,6',7',8',8'a-hexahydro-6'-methoxy-2'-phenyl-pyrano[3,2-d]-[1.3]dioxine}-5-ylidenemalononitrile C22H23N3O5 ÏàËÆ¶È:52.6% Zeitschrift f¨¹r Naturforschung B 2006 61 406-412 Nucleoside Analogues from Push-Pull Functionalized Branched-Chain Pyranosides M. Kordian, H. Feist, W. Kantlehner, M. Michalik, and K. Peseke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . (R)-(+)-5-(2-Hydroxy-3-tosyloxypropyl)-1,3-benzodioxole ÏàËÆ¶È:52.6% European Journal of Organic Chemistry 2012 792-800 Synthesis and Characterization of Adducts Formed in the Reactions of Safrole 2¡ä,3¡ä-Oxide with 2¡ä-Deoxyadenosine, Adenine, and Calf Thymus DNA Li-Ching Shen, Su-Yin Chiang, I-Ting Ho, Kuen-Yuh Wu and Wen-Sheng Chung Structure 13C NMR ̼Æ×Ä£Äâͼ |
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