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331456351: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-27 14:29:41
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331456351: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-27 14:29:41
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²éѯ½á¹û£º¹²²éµ½96¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (E)-ethyl 3-((2R∗,3R∗ -3-cyclohexylaziridin-2-yl)acrylate C13H21NO2 ÏàËÆ¶È:61.5% Tetrahedron 2012 68 2984-2992 Study on the stereochemical control of dihydroxylation of vinyl epoxides and their derivatives Giuliana Righi, Emanuela Mandic¡¯, Gaia Clara Mercedes Naponiello, Paolo Bovicelli, Ilaria Tirotta Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (¡À) 9'-epi-3¦Â,3'¦Â-dimethylxestospongin C C30H54N2O2 ÏàËÆ¶È:60% Planta Medica 2011 77 179-181 9'-Epi-3¦Â,3'¦Â¨Cdimethylxestospongin C, a New Macrocyclic Diamine Alkaloid from the Hainan Sponge Neopetrosia exigua Yan Li, Song Qin, Yue-Wei Guo, Yu-Cheng Gu, Rob W. M. van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3-cyclohexyl-1,2-dimethylimidazolidin-4-one C11H20N2O ÏàËÆ¶È:58.3% Heterocycles 2004 63 1165-1173 A Solvent-free Method for Substituted Imidazolidin-4-ones Synthesis Jir¨ª Posp¨ªsil and Milan Pot¨¢cek* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1 R,4R)-(+)-1-Bromomethyl-3,3-dimethyl-2-methylenebicyclo[2.2.1]heptane ÏàËÆ¶È:58.3% Tetrahedron Letters 2001 42 2261-2263 Rearrangement of methylenecamphor during electrophilic bromination: remarkably clean access to the unnatural fenchyl (1,3,3-trimethylbicyclo[2.2.1]heptane) system Allen A Thomas, Keith A Monk, Sonia Abraham, Stella Lee, Charles M Garner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (1S*,2S*)-1-cyclohexyl-3-(dimethylamino)-2-methyl-1-propanol ÏàËÆ¶È:58.3% 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 -------------------------------------------------------------------------------- 6 . Homononactic Acid ÏàËÆ¶È:58.3% Archiv der Pharmazie 2001 334 143-147 Antifungal Actinomycete Metabolites Discovered in a Differential Cell-Based Screening Using a Recombinant TOPO1 Deletion Mutant Strain Marc Stadler, Frank Bauch, Thomas Henkel, Andrea M¨¹hlbauer, Hartwig M¨¹ller, Frank Spaltmann and Karlheinz Weber Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (S)-N-Cyclohexylmethyl-N-(2-pyrrolidinylmethyl)amine C12H24N2 ÏàËÆ¶È:58.3% Heterocycles 2011 82 1727-1737 Asymmetric Intramolecular Aldol Reaction Mediated by (S)-N-Substituted-N-(2-pyrrolidinylmethyl)amine to Prepare Wieland-Miescher Ketone Yuichi Akahane, Kohei Inomata,* and Yasuyuki Endo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 2 ÏàËÆ¶È:58.3% Journal of the Chemical Society, Perkin Transactions 1 1975 1586-1590 Cyclonerotriol [6-(3-hydroxy-2,3-dimethylcyclopentyl)-2-methylhept-2-ene-1,6-diol], a new sesquiterpenoid metabolite of Fusarium culmorum James R. Hanson, Peter B. Hitchcock and Robert Nyfeler Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 4-trans-hydroxy-2e-methyl-4-ethynyl-trans-decahydroquinoline hydrochloride ÏàËÆ¶È:58.3% Russian Journal of Organic Chemistry 2002 38 1116-1124 Synthesis and Reactions of 4-cis- and 4-trans-Hydroxy-2e-methyl-4-ethynyl-trans-decahydroquinolines S. S. Koval'skaya, N. G. Kozlov and E. A. Dikusar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . racemic 6-hydroxydodecanaoic acid ÏàËÆ¶È:58.3% Heterocycles 2012 85 1061-1075 Enantioselective Synthesis of ¦Å-Lactones by Lipase-Catalyzed Resolution Yasutaka Shimotori,* Masakazu Aoyama, Hidetaka Tsukasa, and Tetsuo Miyakoshi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (¡À/-)-halosaline C10H21NO ÏàËÆ¶È:58.3% Canadian Journal of Chemistry 1996 74 2434-2443 A revised structure for the piperidine alkaloid andrachamine Sibel Mill, Claude Hootel¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . cladioxazole C16H27NO ÏàËÆ¶È:56.2% Tetrahedron Letters 2003 44 6951-6953 Cladioxazole: a novel sesquiterpene from a marine soft coral of genus Cladiella Athar Ata, Joe Ackerman, Parvataneni Radhika Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . ((2S,7S)-7-hexyloxepan-2-yl)methanol C13H26O2 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 8994-9003 Enantiodivergent synthesis of (+)- and (− -isolaurepanGonzalo Pazos, Manuel P¨¦rez, Zoila G¨¢ndara, Generosa G¨®mez, Yagamare Fall Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . compound 23 ÏàËÆ¶È:53.8% Organic Magnetic Resonance 1983 21 Carbon-13 NMR spectra and the method for their calculation for long-chain polybranched carboxylic acids and their derivatives V. I. Dostovalova, A. B. Terent'ev, N. S. Ikonnikov and R. Kh. Freidlina Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Trichoderiol A C15H26O2 ÏàËÆ¶È:53.3% Fitoterapia 2011 82 1035-1038 Sesquiterpenoids from Trichoderma atroviride, an endophytic fungus in Cephalotaxus fortunei Cheng-Jian Zheng, Pei-Xin Sun, Gui-Lin Jin, Lu-Ping Qin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2-cyclohexyl-6-methyl-4-oxo-5-oxa-1-ethoxycarbonyl-1-azaspiro[2,4]bicycloheptane C15H23NO4 ÏàËÆ¶È:53.3% Heterocycles 2005 65 1447-1454 Spiroaziridines from 4-Substituted ¦Á-Ylidene-¦Ã-butyro Lactones Tecla Gasperi, M. Antonietta Loreto,* Antonella Migliorini, and Paolo A. Tardella Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 10 ÏàËÆ¶È:53.3% Australian Journal of Chemistry 1989 42 1591-1603 Tropical Marine Algae. III. New Sesquiterpenes From Laurencia majuscula (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae) JC Coll and AD Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 6-acetamido-1,1,1-trichloroundecane C13H24NOCl3 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 572-577 Polychlorinated Acetamides from the Cyanobacterium Microcoleus lyngbyaceus Michael A. Orsini, Lewis K. Pannell, and Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . comopund 5 C17H34O4 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1990 38 1892-1897 Resin Glycosides. VII. : Reinvestigation of the Component Organic and Glycosidic Acids of Pharbitin, the Crude Ether-Insoluble Resin Glycoside ("Convolvulin" of Pharbitidis Semen (Seeds of Pharbitis nil)Masateru ONO,Naoki NODA,Toshio KAWASAKI and Kazumoto MIYAHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . C-Glycoside III¦Á ÏàËÆ¶È:50% Chemistry of Natural Compounds 1991 27 318-322 13C NMR SPECTRA OF BIOLOGICALLY. ACTIVE COMPOUNDS XI. DIASTEREOMERIC EFFECTS IN C-GLYCOSIDES L. M. Khalilov, A. Yu. Spivak, E. V. Vasil'eva,A. A. Fatykhov, N. A. Prokhorova, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ |
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