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²éѯ½á¹û£º¹²²éµ½38¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2,4-trans-7,4'-dihydroxy-4-methoxyflavan C16H16O4 ÏàËÆ¶È:64.2% Phytochemistry 1998 49 1805-1806 2,4-trans-,7 4¡ä-dihydroxy-4-methoxyflavan from Cassia abbreviata Eckehard Volker Dehmlow, Teunis van Ree, Matthias Guntenhöner Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ferreirinol C16H14O7 ÏàËÆ¶È:55.5% Journal of Natural Products 1996 59 902-903 Ferreirinol, a New 3-Hydroxyisoflavanone from Swartzia polyphylla Jennifer L. DuBois and Albert T. Sneden Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 7¦Â-hydroxy-1-methylene-8¦Á-pyrrolizidine ÏàËÆ¶È:55.5% Phytochemistry 1995 40 1327-1329 The principal alkaloid of Senecio schweinfurthii M. H. Benn, Simon Mathenge, R. M. Munavu, S. O. Were Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . pyrrole-2-propanamide C7H10N2O ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 1996 6 1541-1542 Synthesis of cystamidin a (pyrrole-3-propanamide), a reported calpain inhibitor Ron Bihovsky, Israil Pendrak Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-(4-Hydroxyphenyl)pentane-1,2,5-triol C11H16O4 ÏàËÆ¶È:55.5% Archiv der Pharmazie 2002 335 94-98 Synthesis and Antimicrobial Activity of Hydroxyalkyl-and Hydroxyacyl-phenols and Their Benzyl Ethers J¨¹rgen Krauß and D. Unterreitmeier Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-Cyano-2-hydroxymethylbenzimidazole C9H7N3O ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2000 8 1371-1382 2''-Substituted 5-phenylterbenzimidazoles as topoisomerase I poisons Meera Rangarajan, Jung Sun Kim, Song Jin, Sai-Peng Sim, Angela Liu, Daniel S. Pilch, Leroy F. Liu, Edmond J. LaVoie Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-(4-Methoxyphenyl)dihydrofuran-2(3H)-one C11H12O3 ÏàËÆ¶È:55.5% Tetrahedron 2012 68 4145-4151 Baeyer¨CVilliger Oxidation of Cyclobutanones with 10-Methylacridinium as an Efficient Organocatalyst Original Research Article Hua-Jian Xu, Feng-Fei Zhu, Yong-Ya Shen, Xin Wan, Yi-Si Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 9f C8H6O3Br2S2 ÏàËÆ¶È:55.5% Heterocycles 2000 52 365-382 Synthesis, Isolation, and Dimerization and Trimerization of Monosubstituted Thiophene 1,1-Dioxides Juzo Nakayama,* Hidehiro Nagasawa, Yoshiaki Sugihara, and Akihiko Ishii Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N-(4-methoxyphenyl)-N-(thietan-3-yl)methanesulfonamide C11H15NO3S2 ÏàËÆ¶È:55.5% Russian Journal of Organic Chemistry 2005 41 1023-1035 Reactions of 2-(¦Á-Haloalkyl)thiiranes with Nucleophilic Reagents: IV. Alkylation of Sulfonamides with 2-Chloromethylthiirane. Synthesis and Properties of 3-(Arylamino)thietanes V. V. Sokolov, A. N. Butkevich, V. N. Yuskovets, A. A. Tomashevskii and A. A. Potekhin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . vanillin C8H8O3 ÏàËÆ¶È:55.5% Journal of the Chinese Chemical Society 2009 56 600-605 Palaeophytochemical Components from the Miocene-Fossil Wood of Pinus griffithii Jian-Rong Luo, Qing-Yun Ma, You-Xing Zhao,Tie-Mei Yi, Cheng-Sen Li and Jun Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 2 ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2011 908-911 Copper-Catalyzed Intramolecular C¨CH Amination Dipti N. Barman and Kenneth M. Nicholas Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . bis(methyl 6-deoxy-¦Á--mannopyranosid-6-yl)sulfane C14H26O10S ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2010 1951-1970 Non-Glycosidically Linked Pseudodisaccharides: Thioethers, Sulfoxides, Sulfones, Ethers, Selenoethers, and Their Binding to Lectins Ian Cumpstey, Clinton Ramstadius, Tashfeen Akhtar, Irwin J. Goldstein and Harry C. Winter Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-methyl-¦Á-{1-[tris(1-methylethyl)silyl]propa-1,2-dien-1-yl}benzenemethanol ÏàËÆ¶È:55.5% Helvetica Chimica Acta 2012 95 1773-1789 Gold(I)-Catalyzed Cyclodehydration Enabled by the Triisopropylsilyl Group: A Synthetically Versatile Methodology Dmitry L. Usanov, Marina Naodovic, Malte Brasholz and Hisashi Yamamoto Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . N-[2,2,2-trichloro-1-(1-methyl-1H-pyrrol-3-yl)-ethyl]benzenesulfonamide ÏàËÆ¶È:54.5% Russian Journal of Organic Chemistry 2009 45 1365-1374 C-amidoalkylation of pyrroles with N-trifluoromethylsulfonyl and N-arylsulfonyl polychloroaldehyde imines E. V. Kondrashov, E. V. Rudyakova, G. N. Rozentsveig, I. B. Rozentsveig and K. A. Chernyshev, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . viridoside C15H22O7 ÏàËÆ¶È:53.8% Natural Product Communications 2008 3 53-56 Phenolic Glycosides from Phlomis lanceolata (Lamiaceae) Hossein Nazemiyeh, Abbas Delazar, Mohammed-Ali Ghahramani, Amir-Hossein Talebpour,Lutfun Nahar and Satyajit D. Sarker Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 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:50% 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 17 . 1-(4-hydroxyphenyl)-2-(3,5-dihydroxyphenyl)-2-hydroxyethanone C14H12O5 ÏàËÆ¶È:50% Phytochemistry 2007 68 2432-2438 Anti-oxidant constituents from Sedum takesimense Phuong Thien Thuong, Ho Jeong Kang, MinKyun Na, WenYi Jin, Ui Jung Youn,Yeon Hee Seong, Kyung-Sik Song, Byung-Sun Min, KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-hydroxyeugenol ÏàËÆ¶È:50% Phytochemistry 2007 68 1464-1470 Ericifolin: An eugenol 5-O-galloylglucoside and other phenolics from Melaleuca ericifolia S.A.M. Hussein, A.N.M. Hashi, R.T. El-Sharawy, M.A. Seliem, M. Linscheid,U. Lindequist, M.A.M. Nawwar Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (1Z,3E,5R*,6S*)-1-bromo-5,6-dichloro-2,6-dimethyl-octa-1,3,7-triene C10H13BrCl2 ÏàËÆ¶È:50% Phytochemistry 2009 70 597-600 Antiplasmodial halogenated monoterpenes from the marine red alga Plocamium cornutum Anthonia F. Afolayan, Maryssa G.A. Mann, Carmen A. Lategan, Peter J. Smith, John J. Bolton, Denzil R. Beukes Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1-deoxy-1-(4-hydroxyphenyl)-¦Á-tagatopyranose ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1999 47 1618-1625 Studies on Nepalese Crude Drugs. XXVI. Chemical Constituents of Panch Aunle, the Roots of Dactylorhiza hatagirea D. DON. Haruhisa KIZU,Ei-ichi KANEKO and Tsuyoshi TOMIMORI Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2-hydroxy-3-methoxy-5-(2-propenyl)phenol C10H12O3 ÏàËÆ¶È:50% Phytochemistry 1997 46 1063-1067 Isofuranonaphthoquinones and phenolic and knipholone derivatives from the roots of Bulbine capitata Merhatibeb Bezabih, Selebo Motlhagodi, Berhanu M. Abegaz Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (Z)-2-(4-hydroxyphenyl)ethenyl-¦Á-L-rhamnopyranoside ÏàËÆ¶È:50% Phytochemistry 1997 45 149-157 Joannesialactone and other compounds from Joannesia princeps Hans Achenbach, Gerd Benirschke Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 2-ôÇ»ù-4-¼×Ñõ¼×Ñõ»ù±½ÒÒͪ ÏàËÆ¶È:50% Chemical Journal of Chinese Universities 2010 31 1342-1345 Modified Total Synthesis of Verbenachalcone ZHANG Ying-Peng,CHEN Yu-Tao,YANG Yun-Shang,GUAN Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 2-(5-Iodo-1H-indol-3-yl)-2-(hydroxyamino)ethanamine dihydrochloride ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 3204-3215 Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents Olga N. Burchak,Emmanuelle Le Pihive, Laure Maigre, Xavier Guinchard , Pascale Bouhours ,Claude Jolivalt, Dominique Schneider , Max Maurin , Carmela Giglione , Thierry Meinnel ,Jean-Marc Paris , Jean-Noël Denis Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 1-(4-methoxyphenyl)pyrrole-2-carbonitrile C12H10N2O ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2006 43 681-684 Anodic cyanation of 1-arylpyrroles Wei Liu,Yuan Ma,Yu-Fen Zhao and Ying-Wu Yin Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2,4-dibromo-5-(1-hydroxy-p-methoxyphenylmethyl)pyrimidine ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 509-513 Metalation of bromodiazines. Diazines XL Laurence Decrane,Nelly Pl¨¦ and Alain Turck Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . (2S*,3S*,5S*)-2-(4-fluorophenyl)-5-(methanesulfonyloxymethyl)tetrahydrofuran-3-ol C12H15O5FS ÏàËÆ¶È:50% Heterocycles 2006 68 1429-1442 Synthesis of Tetrahydrofurfurylamines Related to Muscarine Roberto Fern¨¢ndez de la Pradilla,* Pilar Manzano, Alma Viso, Javier Fern¨¢ndez, and Antonio G¨®mez Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (5-bromoindo-1-yl)acetonitrile C10H7N2Br ÏàËÆ¶È:50% Heterocycles 2003 60 865-877 Synthesis of New Melatonin Analogues from Dimers of Azaindole and Indole by Use of Suzuki Homocoupling J¨¦rôme Guillard, Carlos Larraya, and Marie-Claude Viaud-Massuard* Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 1-Ethyl-1H-indole-2,3-dione 3-Oxime C10H10N2O2 ÏàËÆ¶È:50% Helvetica Chimica Acta 2010 93 2454-2466 Microwave-Assisted Three-Component Synthesis of Some Novel 1-Alkyl-1H-indole-2,3-dione 3-(O-Alkyl-oxime) Derivatives as Potential Chemotherapeutic Agents Mohammad Navid Soltani Rad, Ali Khalafi-Nezhad, Somayeh Babamohammadi and Somayeh Behrouz Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . salidroside ÏàËÆ¶È:50% Phytochemistry 1977 16 2036-2038 Dihydrochalcones from Viburnum davidii and V. lantanoides Søren Rosendal Jensen, Bent Juhl Nielsen, Viggo Norn Structure 13C NMR ̼Æ×Ä£Äâͼ |

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