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summerxkgao: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-03-16 14:26:36
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summerxkgao: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-03-16 14:26:36
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²éѯ½á¹û£º¹²²éµ½2265¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Methyl 2-Butyl-4,5,6,7-tetrahydrobenzofuran-3-carboxylate C14H20O3 ÏàËÆ¶È:76.9% The Journal of Organic Chemistry 2012 77 8657-8668 Synthesis of Furan-3-carboxylic and 4-Methylene-4,5-dihydrofuran-3-carboxylic Esters by Direct Palladium Iodide Catalyzed Oxidative Carbonylation of 3-Yne-1,2-diol Derivatives Bartolo Gabriele, Raffaella Mancuso, Vito Maltese, Lucia Veltri, and Giuseppe Salerno Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 5-Bromo-1,4-dimethyl-6-pentyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine C14H21N2Br ÏàËÆ¶È:71.4% Bioorganic & Medicinal Chemistry 2012 20 3584-3595 Simplified bicyclic pyridinol analogues protect mitochondrial function Xiaoqing Cai, Omar M. Khdour, Jennifer Jaruvangsanti, Sidney M. Hecht Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . octanoic acid ÏàËÆ¶È:71.4% Zeitschrift f¨¹r Naturforschung C 1999 54 70-74 Inhibition of Mushroom Tyrosinase by Kojic Acid Octanoates H. Kaatz, K. Streffer, U. Wollenberger and M. G. Peter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 6-n-pentyl-2H-pyran-2-one (6PAP) ÏàËÆ¶È:69.2% Journal of Natural Products 1997 60 1242-1244 Microbial Transformation of the Trichoderma Metabolite 6-n-Pentyl-2H-pyran-2-one Janine M. Cooney, Denis R. Lauren, Philip R. Poole, and Giles Whitaker Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 5/6 C13H17N5S ÏàËÆ¶È:69.2% Journal of Heterocyclic Chemistry 2003 40 813-820 On triazoles XLVII. Synthesis of 1,3a,5,6,¦Øc-pentaazacycloalka[e]acenaphthylenes G¨¢bor Berecz and J¨®zsef Reiter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 6-pentyl-¦Á-pyrone ÏàËÆ¶È:69.2% Bioscience, Biotechnology, and Biochemistry 1997 61 1428-1433 Two Oxazolyl Compounds and a Monosubstituted ¦Á-Pyrone as Free-radical Scavengers Isolated from a Fungus Yasujiro MORIMITSU, Akira HIROTA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound VIa ÏàËÆ¶È:69.2% Russian Journal of Organic Chemistry 2004 40 1427-1431 Acid-catalyzed reactions of epoxides derived from citronellene T. M. Khomenko, D. V. Korchagina and V. A. Barkhash Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound VIb ÏàËÆ¶È:69.2% Russian Journal of Organic Chemistry 2004 40 1427-1431 Acid-catalyzed reactions of epoxides derived from citronellene T. M. Khomenko, D. V. Korchagina and V. A. Barkhash Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound VIIa C12H21NO ÏàËÆ¶È:69.2% Russian Journal of Organic Chemistry 2004 40 1427-1431 Acid-catalyzed reactions of epoxides derived from citronellene T. M. Khomenko, D. V. Korchagina and V. A. Barkhash Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound VIIb C12H21NO ÏàËÆ¶È:69.2% Russian Journal of Organic Chemistry 2004 40 1427-1431 Acid-catalyzed reactions of epoxides derived from citronellene T. M. Khomenko, D. V. Korchagina and V. A. Barkhash Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 5 C12H22O3 ÏàËÆ¶È:69.2% European Journal of Organic Chemistry 2010 856-861 Titanocene-Promoted Eliminations on Epoxy Alcohols and Epoxy Esters Alfonso Fern¨¢ndez-Mateos, Soledad Encinas Madrazo, Pablo Herrero Teij¨®n and Rosa Rubio Gonz¨¢lez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Methyl 2-Butyl-4,5-dimethylfuran-3-carboxylate C12H18O3 ÏàËÆ¶È:69.2% The Journal of Organic Chemistry 2012 77 8657-8668 Synthesis of Furan-3-carboxylic and 4-Methylene-4,5-dihydrofuran-3-carboxylic Esters by Direct Palladium Iodide Catalyzed Oxidative Carbonylation of 3-Yne-1,2-diol Derivatives Bartolo Gabriele, Raffaella Mancuso, Vito Maltese, Lucia Veltri, and Giuseppe Salerno Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . N-(2-Iodooctyl)-4-methylbenzenesulfonamide ÏàËÆ¶È:69.2% Chinese Journal of Chemistry 2013 31 1508-1512 An Improved Protocol for Regioselective Ring-Opening of Sulfonyl Aziridines with Iodine Promoted by PPh3 Jinfeng Zhang, Lingguo Meng, Chuntao Li and Guoyuan Xiao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . cubenene ÏàËÆ¶È:66.6% Phytochemistry 1991 30 1551-1554 Oxygenated sesquiterpenes from the wood of Juniperus oxycedrus A.F. Barrero, J.F. S¨¢nchez, J.E. Oltra, J. Altarejos, N. Ferrol, A. Barrag¨¢n Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ( +)-ent-Cubenene ÏàËÆ¶È:66.6% Phytochemistry 1982 21 233-234 (+)-Ent-epicubenol from the liverwort Scapania undulata Joseph D. Connolly, William R. Phillips, Siegfried Huneck Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . cadinane-4(14),5-diene ÏàËÆ¶È:64.2% Phytochemistry 1994 37 1327-1330 Sesquiterpenes from the brown alga Taonia atomaria Salvatore De Rosa, Alfonso De Giulio, Carmine Iodice, Nevenka Zavodink Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1'(2'),3'(4')-tetrahydro-gregatin B ÏàËÆ¶È:64.2% Natural Product Communications 2015 Vol. 10 No. 1 107−111 Pulvinulin A, Graminin C, and cis-Gregatin B ¨C New Natural Furanones from Pulvinula sp. 11120, a Fungal Endophyte of Cupressus arizonica E. M. Kithsiri Wijeratne, Yaming Xu, A. Elizabeth Arnold and A. A. Leslie Gunatilaka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 4/3 C16H24N6OS ÏàËÆ¶È:64.2% Journal of Heterocyclic Chemistry 2002 39 703-718 On triazoles XLVI. Synthesis of 1,3a,5,6,10c-pentaazaacephenanthrylenes Gabor Berecz, L¨¢szl¨® P¨¢rk¨¢nyi, J¨®zsef Reiter and Alajos K¨¢lm¨¢n Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . secoswartzianin A C15H20O2 ÏàËÆ¶È:64.2% Tetrahedron Letters 1993 34 3753-3754 Structure of secoswartzianins A and B isolated from the liverwort Porella swartziana Motoo Tori, Katsuyuki Nakashima, Tomoko Takeda, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . tert-Butyl 7-methyl-3-oxoundecanoate ÏàËÆ¶È:64.2% Bioscience, Biotechnology, and Biochemistry 2010 74 119-124 Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth Tomonori TAGURI, Rei YAMAKAWA, Yasushi ADACHI, Kenji MORI and Tetsu ANDO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . pellitorine ÏàËÆ¶È:64.2% Canadian Journal of Chemistry 2004 82 622-630 Stereoselective synthesis of naturally occurring unsaturated amide alkaloids by a modified RambergBäcklund reaction Yang Li, Yu Zhang, Zhi Huang, Xiaoping Cao, Kun Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . pellitorine C14H25NO ÏàËÆ¶È:64.2% Journal of Chromatography A 2004 1040 193-204 Preparative isolation and purification of amides from the fruits of Piper longum L. by upright counter-current chromatography and reversed-phase liquid chromatography Shihua Wu, Cuirong Sun, Saifeng Pei, Yanbin Lu, Yuanjiang Pan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . dimethyl 2-((2-(butylamino)-6-oxocyclohex-1-enyl)methyl)malonate C16H25NO5 ÏàËÆ¶È:64.2% Tetrahedron 2013 69 9406-9416 Lithium perchlorate-, acetic anhydride-, and triphenylphosphine-assisted multicomponent syntheses of 4-unsubstituted 2,5-dioxooctahydroquinoline-3-carboxylates and 3-carbonitriles Original Research Article Xingxian Gu, Gunda I. Georg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . 6-[Azepan-2-ylideneamino]-5-bromo-1-isobutylpyrimidine-2,4(1H,3H)-dione C14H21BrN4O2 ÏàËÆ¶È:64.2% Tetrahedron 2012 68 8564-8571 An approach to alicyclic ring-fused xanthines Kostiantyn Liubchak, Andrey Tolmachev, Oleksandr O. Grygorenko, Kostiantyn Nazarenko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . Ethyl 2-Butyl-4,5,6,7-tetrahydrobenzofuran-3-carboxylate C15H22O3 ÏàËÆ¶È:64.2% The Journal of Organic Chemistry 2012 77 8657-8668 Synthesis of Furan-3-carboxylic and 4-Methylene-4,5-dihydrofuran-3-carboxylic Esters by Direct Palladium Iodide Catalyzed Oxidative Carbonylation of 3-Yne-1,2-diol Derivatives Bartolo Gabriele, Raffaella Mancuso, Vito Maltese, Lucia Veltri, and Giuseppe Salerno Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 5/10 C18H27N5S ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2003 40 813-820 On triazoles XLVII. Synthesis of 1,3a,5,6,¦Øc-pentaazacycloalka[e]acenaphthylenes G¨¢bor Berecz and J¨®zsef Reiter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . (+)-(1R,2R,4S,6R,7S,9S)-4-isopropenyl-1,5,5,6,7-pentamethyltricyclo[4.3.0.02,9]nonan-8-one |

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