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  • Palladium-Catalyzed 2-Arylation of Pyrroles
    [作者:GRYKO DANIEL T; VAKULIUK OLENA; GRYKO DOROTA; KOSZARNA BEATA,期刊:Journal of Organic Chemistry, 页码:9517-9520 , 文章类型: Article,,卷期:2009年74-24]
  • A methodology that affords N-alkyl-2-arylpyrroles and N-aryl-2-arylpyrroles via direct coupling from aryl iodides has been developed. After examining various reaction parameters: solvent, ratio of reagents, catalyst, bas...
  • A Facile and Practical Synthesis of N-Acetyl Enamides
    [作者:TANG WENJUN; CAPACCI ANDREW; SARVESTANI MAX; WEI XUDONG; YEE NATHAN K; SENANAYAKE CHRIS H,期刊:Journal of Organic Chemistry, 页码:9528-9530 , 文章类型: Article,,卷期:2009年74-24]
  • A facile and practical method for the synthesis of N-acetyl alpha-arylenamides has been developed from corresponding ketoximes as the starting materials with ferrous acetate as the reducing reagent. This methodology offe...
  • Reduction of Solid-Supported Olefins and Alkynes
    [作者:DICKSON DAVID P; TOH CHRISTINE; LUNDA MENAKA; YERMOLINA MARIA V; WARDROP DUNCAN J; LANDRIE CHAD L,期刊:Journal of Organic Chemistry, 页码:9535-9538 , 文章类型: Article,,卷期:2009年74-24]
  • The reduction of carbon-carbon multiple bonds in alkynes and olefins supported on a polystyrene resin has been investigated. Homogeneous catalysis by titanocene reagents is effective for the stereoselective preparation o...
  • Synthesis of a TRPV1 Receptor Antagonist
    [作者:YU SU; HAIGHT ANTHONY; KOTECKI BRIAN; WANG LEI; LUKIN KIRILL; HILL DAVID R,期刊:Journal of Organic Chemistry, 页码:9539-9542 , 文章类型: Article,,卷期:2009年74-24]
  • A five-step synthesis of a TRPV1 receptor antagonist 1 is described. The key step involves a novel palladium-catalyzed amidation reaction of 4-chloro-1-methylindazole 8 with the benzyl urea 9 to form the unsymmetrically ...
  • Asymmetric Total Synthesis of (+)-Crassalactone D
    [作者:YANG ZHICAI; TANG PHUNG; GAUUAN JOLICIA F; MOLINO BRUCE F,期刊:Journal of Organic Chemistry, 页码:9546-9549 , 文章类型: Article,,卷期:2009年74-24]
  • The asymmetric total synthesis of (+)-crassalactone D (4), a naturally occurring antitumor agent, has been achieved by employing an oxidative spirocyclization of furan 11 as the key step. Two close analogues, 7-epi-crass...