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PSA: ½ð±Ò+1, ÔٴθÐл 2013-01-23 16:32:23
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»¯ºÏÎï1£º ²éѯ½á¹û£º¹²²éµ½20¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . trans-3,7-Dimethyl-2,6-octadien-l-trilp henylphosphoniumbromid ÏàËÆ¶È:57.1% Helvetica Chimica Acta 1980 63 1367-1376 1,2-Epoxy-Carotinoide. 1. Mitteilung. Synthese von 1,2-Epoxy-lycopin und 1,2,1',2'-Diepoxy-lycopin Hanspeter Pfander, Matthias Kamber, Yvonne Battegay-Nussbaumer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3,4-dioxo-4-piperidino-2-(1,1,1-triphenyl-¦Ë5-phosphanylidene)butanenitrile C27H26N2O2P ÏàËÆ¶È:53.8% Tetrahedron Letters 2000 41 2511-2514 The chemistry of vicinal tricarbonyls. Formation of oxomalondiamides Harry H. Wasserman, Kieseung Lee, Mingde Xia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 3 C12H18O2 ÏàËÆ¶È:53.8% Tetrahedron Letters 2000 41 9655-9659 New synthetic methodology for ring expansion of n-sized conjugated cycloalkenones into homoallylic n+3 lactones: 3-step synthesis of fragrant phoracantholide Gary H. Posner, Qiang Wang, Bethany A. Halford, Jeffrey S. Elias, John P. Maxwell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1S*,2S*)-1-cyclohexyl-3-(dimethylamino)-2-methyl-1-propanol ÏàËÆ¶È:53.8% Tetrahedron Letters 2001 42 8811-8815 One-pot highly stereoselective reduction of ¦Â-keto amides to syn-¦Ã-aminols Giuseppe Bartoli, Marcella Bosco, Renato Dalpozzo, Enrico Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 2-(1-cyclohexen-1-yl)-2-cyclohexen-1-ol C12H18O ÏàËÆ¶È:53.8% Tetrahedron 2002 58 5163-5172 Six- and five-membered 3-alkoxy-2-lithiocycloalkenes: new stable non-anionic ¦Â-functionalised organolithium compounds Miguel Yus, Diego J Ram¨®n, Inmaculada G¨®mez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (6a¦Á,7a¦Â,7b¦Á,13a¦Á,13b¦Â,14b¦Á)-or (6a¦Á,7a¦Á,7b¦Â,13a¦Â,13b¦Á,14b¦Á)-7a,13b-dichloro-1,2,3,4,5,6,6a,7a,7b,8,9,10,11,12,13,13a,13b,14b-octadecahydrobenzo[1,''2'':3,4;4'',5'':3',4']dicyclobuta[1,2:1',2']dicyclooctene-7,14-dione C22H28Cl2O2 ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2011 968-982 Photochemical Reactions of Chloranil with Cyclooctene, 1,5-Cyclooctadiene, and Cyclohexene Revisited Manfred Christl, Max Braun, Oliver Deeg and Stephan Wolff Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (3R,4S)-3-[(tert-butyldimethylsilyl)oxy]-4-cyclohexyl-2-azetidinone C15H29NO2Si ÏàËÆ¶È:53.8% Journal of Medicinal Chemistry 1994 37 3337-3343 The Effect of the Aromatic Rings of Taxol on Biological Activity and Solution Conformation: Synthesis and Evaluation of Saturated Taxol and Taxotere Analogs Thomas C. Boge, Richard H. Himes, David G. Vander Velde, Gunda I. Georg Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 3a C17H29NO2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1987 35 928-931 FOUR NEW BISABOLENE-TYPE AMINOSESQUITERPENES FROM AN OKINAWAN MARINE SPONGE, THEONELLA SP. (THEONELLIDAE) Isao Kitagawa,Norihito Yoshioka,Chikayo Kamba,Masayuki Yoshikawa and Yoshihiro Hamamoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 4a C17H29NO2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1987 35 928-931 FOUR NEW BISABOLENE-TYPE AMINOSESQUITERPENES FROM AN OKINAWAN MARINE SPONGE, THEONELLA SP. (THEONELLIDAE) Isao Kitagawa,Norihito Yoshioka,Chikayo Kamba,Masayuki Yoshikawa and Yoshihiro Hamamoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 6,7,9,10-tetrahydroasteriscunolide C15H22O3 ÏàËÆ¶È:53.3% Natural Product Research 2001 15 419-423 Isolation and Structure Determination of a New Sesquiterpene Lactone from Nauplius aquaticus Atef Chaari; Hichem B. Jannet; Zine Mighri; Christine Robinot; Nicole Kunesch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (E )-6¦Á,11-dihydroxy-7¦ÁH-germacra-4,10(14)-dien-1-one C18H30O3 ÏàËÆ¶È:53.3% Phytochemistry 1999 51 529-541 Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring Alejandro F. Barrero, M. Mar Herrador, Jose F.Quilez, Ramon Alvarez-Manzaneda, Dolores Portal, Jose A. Gavin, Dolores G. Gravalos, M.S.J. Simmonds, W.M. Blaney Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (3S,3aR,4S,6R,7aS)-4-hydroxy-6-[(methanesulfonyl)oxy]-3-(4-methyl-3-pentenyl)-3a,4,5,6,7,7a-hexahydrobenzofuran-2(3H)-one C15H24O6S ÏàËÆ¶È:53.3% Tetrahedron 1999 55 3855-3870 Total synthesis of paniculide A from d-glucose Seiji Amano, Noriaki Takemura, Masami Ohtsuka, Seiichiro Ogawa, Noritaka Chida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Deoxyshikonin ÏàËÆ¶È:50% Natural Product Sciences 2007 13 328-331 Farnesyl Protein Transferase Inhibitory Components of Lithospermum erythrorhizon Kim, Seong-Jin; Kwon, Byoung-Mog; Kim, Sung-Hoon; Baek, Nam-In; Yang, Jae-Heon; Lee, Jeong-Joo; Lee, Sa-Im; Kwon, Young-Ee; Park, Hee-Wook; Lee, Jae-Hyeok; Park, Jeong-Suk; Kim, Dae-Keun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (E)-2,6,10-trimethylundeca-5,9-dienal C14H24O ÏàËÆ¶È:50% Organic Letters 2006 Vol. 8, No. 2 321-324 Liphagal, a Selective Inhibitor of PI3 Kinase ¦Á Isolated from the Sponge Aka coralliphaga: Structure Elucidation and Biomimetic Synthesis Frederic Marion,David E. Williams,Brian O. Patrick, Irwin Hollander,Robert Mallon,Steven C. Kim, Deborah M. Roll, Larry Feldberg,Rob Van Soest, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 5i C20H17N2PO4Cl6 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2004 41 1001-1004 Synthesis and antimicrobial activity of N-(substituted)-N-[1,2,4,8,10,11-hexachloro-6-oxido-12H-dibenzo(d,g)(1,3,2)-dioxaphosphocin-6-yl]ureas P. Haranath,U. Anasuyamma,P. Vasu Govardhana Reddy and C. Sureshx Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . tert-butyl (4R)-4-[(tert-butoxy-carbonyl) amino]-5-phenylpentanoate ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2002 12 3431-3433 Novel spirocyclic pyrrolidones as P2/P1 mimetics in potent inhibitors of HIV-1 protease Wieslaw M. Kazmierski, Eric Furfine, Andrew Spaltenstein, Lois L. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Z-antiepilepsirine C15H17NO3 ÏàËÆ¶È:50% Fitoterapia 2010 81 632-635 New amide alkaloid from the aerial part of Piper capense L.f. (Piperaceae) Ali Mohamed Kaou, Val¨¦rie Mahiou-Leddet, C¨¦cile Canlet, Laurent Debrauwer, S¨¦bastien Hutter, Nadine Azas, Evelyne Ollivier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . methyl (5S,7R)-7-acetoxy-5-(1-methyl-1-chloro-ethyl)-8-oxonon-2-enoate C15H23ClO5 ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2008 44 1606-1610 Synthesis-freindly chiral ¦Á-hydroxymethyl ketones from (-)-carvone F. A. Gimalova, N. K. Selezneva, L. S. Khasanova, Kh. F. Sagitdinova and M. S. Miftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (1-(allyloxy)(8-(tert-butyl)dimethylsiloxy))octane C17H36O2Si ÏàËÆ¶È:50% Tetrahedron 2012 68 9769-9776 Elaboration of the ether cleaving ability and selectivity of the classical Pearlman's catalyst [Pd(OH)2/C]: concise synthesis of a precursor for a myo-inositol pyrophosphate Alson Mart, Mysore S. Shashidhar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . tuberatolide A C18H26O3 ÏàËÆ¶È:50% Journal of Natural Products 2011 74 90-94 Tuberatolides, Potent FXR Antagonists from the Korean Marine Tunicate Botryllus tuberatus Hyukjae Choi, Hoosang Hwang, Jungwook Chin, Euno Kim, Jaehwan Lee, Sang-Jip Nam, Byoung Chan Lee, Boon Jo Rho, and Heonjoong Kang Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2£º 1 . nectandrin B C20H24O5 ÏàËÆ¶È:69.2% Acta Botanica Yunnanica 1997 19(2) 211-212 CHEMICAL CONSTITUENTSOF PIPER POLYSYPHORUM Zhang Ke, ¡¡Chen Changxiang, ¡¡Chen Defang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Salicifoliol C13H14O5 ÏàËÆ¶È:69.2% 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:69.2% 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:69.2% 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. LÜ Jing, JIA Ling-yun, YUAN Jiu-zhi, ZHANG Jing-jiao, SUN Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-(7S,8R,8'R)-4,8'-Dihydroxy-3-methoxy-1',2',3',4',5',6'-hexanorligna-7',7-lactone C13H16O5 ÏàËÆ¶È:61.5% Journal of Natural Products 2009 72 2145-2152 Chemical Constituents of the Bark of Machilus wangchiana and Their Biological Activities Wei Cheng, Chenggen Zhu,Wendong Xu, Xiaona Fan,Yongchun Yang,Yan Li,Xiaoguang Chen, Wenjie Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . nectandrin B ÏàËÆ¶È:61.5% Natural Product Research and Development 2010 22 987-990 Chemical Constituents of Myristica argentea Warb. SHI Ji; ZHAO Qi-miao; JIA Tia-zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (E)-Coniferyl Ethyl Ether ÏàËÆ¶È:61.5% Journal of Agricultural and Food Chemistry 2006 54 8848-8854 Characterization of the Chemical Composition of a Byproduct from Siam Benzoin Gum Cecilia Castel, Xavier Fernandez, Louisette Lizzani-Cuvelier, Christine Perichet, and Sophie Lavoine Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . nectandrin B ÏàËÆ¶È:61.5% Journal of the Brazilian Chemical Society 2009 20 1110-1118 Biological Activities of Lignoids from Amazon Myristicaceae Species: Virola michelii, V. mollissima, V. pavonis and Iryanthera juruensis (dedicated to Prof. Otto R. Gottlieb) Sabrina K. R. Morais, Ana F. Teixeira, Zelina E. dos S. Torres, Sergio M. Nunomura, Edite H. Y. Kanashiro, Jos¨¦ Angelo L. Lindoso and Massayoshi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (3S,4S,5S)-5-(4-benzyloxy-3-methoxyphenyl)-3,4-dimethyldihydrofuran-2-one C20H22O4 ÏàËÆ¶È:61.1% Heterocycles 2008 76 551-567 Synthesis of (¡ª)-Talaumidin, a Neurotrophic 2, 5-Biaryl-3, 4-dimethyltetrahydrofuran Liganan, and Its Stereoisomers Yoshiyasu Fukuyama, Kenichi Harada, Tomoyuki Esumi, Daisuke Hojyo, Yumemi Kujime, Naoko Kubo, Miwa Kubo, and Hideaki Hioki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 3 ÏàËÆ¶È:57.1% European Journal of Organic Chemistry 1988 1988 1043-1047 A new member of the class of antibiotics with thiotetronic acid structure isolated from Streptomyces olivaceus T¨¹ 3010 Claudius Rapp, G¨¹nther Jung, Caroline Isselhorst-Scharr and Hans Zähner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 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:53.8% 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 -------------------------------------------------------------------------------- 12 . (+)-(7S,8R)-4-Hydroxy-3-methoxy-1',2',3',4',5',6',7'-heptanorlign-8'-one C12H16O4 ÏàËÆ¶È:53.8% Journal of Natural Products 2009 72 2145-2152 Chemical Constituents of the Bark of Machilus wangchiana and Their Biological Activities Wei Cheng, Chenggen Zhu,Wendong Xu, Xiaona Fan,Yongchun Yang,Yan Li,Xiaoguang Chen, Wenjie Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . bisbenzopyran C20H22O6 ÏàËÆ¶È:53.8% 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 -------------------------------------------------------------------------------- 14 . coniferyl alcohol ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 1982 30 1525-1527 BALANOPHONIN, A NEW NEO-LIGNAN FROM BALANOPHORA JAPONICA MAKINO Mitsumasa Haruna,Tomoko Koube,Kazuo Ito and Hiroyuki Murata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . d-pinoresinol ÏàËÆ¶È:53.8% 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 -------------------------------------------------------------------------------- 16 . pinoresinol C20H22O6 ÏàËÆ¶È:53.8% 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 -------------------------------------------------------------------------------- 17 . 1-O-methyl-guaiacylglycerol C11H16O5 ÏàËÆ¶È:53.8% China Journal of Chinese Materia Medica 2009 34 1672-1675 Chemical constituents from roots of Incarvillea mairei HUANG Zhengsheng, ZHANG Weidong, LIN Sheng, LIU Chunmei, HUANG Dasen, SONG Taifa, LU Longhai, PEI Yuehu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (+)-pinoresinol ÏàËÆ¶È:53.8% 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 -------------------------------------------------------------------------------- 19 . 3,4-dimethoxycinnamyl alcohol ÏàËÆ¶È:53.8% 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 -------------------------------------------------------------------------------- 20 . pinoresinol C20H22O6 ÏàËÆ¶È:53.8% 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 -------------------------------------------------------------------------------- 21 . pinoresinol C20H22O6 ÏàËÆ¶È:53.8% Fitoterapia 2001 72 80-82 Lignans from Strophanthus gratus S. Cowan, M. Stewart, D.K. Abbiw, Z. Latif ,S.D. Sarker,U, R.J. Nash Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (¡À) pinoresinol ÏàËÆ¶È:53.8% Phytochemistry 2000 54 897-899 Spectral comparisons of coniferyl and cinnamyl alcohol epoxide derivatives with a purported cis-epoxyconiferyl alcohol isolate Nathan R. Guz, Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ |

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