CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 2002, Vol. 74, No. 1, pp. 143-149

http://dx.doi.org/10.1351/pac200274010143

Metal-assisted amination with oxime derivatives

Koichi Narasaka

Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Gulevich Anton V., Dudnik Alexander S., Chernyak Natalia, Gevorgyan Vladimir: Transition Metal-Mediated Synthesis of Monocyclic Aromatic Heterocycles. Chem. Rev. 2013, 113, 3084. <http://dx.doi.org/10.1021/cr300333u>
  • Liu Hailan, Yan Xiaoyu, Chen Chao, Liu Qingbin, Xi Chanjuan: Copper-mediated electrophilic imination of alkenylzirconocenes with O-benzoyl ketoximes and aldoximes. Chem. Commun. 2013, 49, 5513. <http://dx.doi.org/10.1039/c3cc41574k>
  • John Alex, Nicholas Kenneth M.: Copper-Mediated Multiple C–H Functionalization of Aromatic N-Heterocycles: Bromoamination of Indoles and Pyrroles. Organometallics 2012, 31, 7914. <http://dx.doi.org/10.1021/om300553b>
  • Beletskaya Irina P., Cheprakov Andrei V.: The Complementary Competitors: Palladium and Copper in C–N Cross-Coupling Reactions. Organometallics 2012, 31, 7753. <http://dx.doi.org/10.1021/om300683c>
  • Ren Zhi-Hui, Zhang Zhi-Yuan, Yang Bing-Qin, Wang Yao-Yu, Guan Zheng-Hui: Copper-Catalyzed Coupling of Oxime Acetates with Aldehydes: A New Strategy for Synthesis of Pyridines. Org Lett 2011, 13, 5394. <http://dx.doi.org/10.1021/ol202290y>
  • Liu Hui, Wang Limin, Tong Xiaofeng: Palladium-catalyzed Heck-type reaction of oxime ether bearing a pendant vinyl iodide moiety. Chem Commn 2011, 47, 12206. <http://dx.doi.org/10.1039/c1cc15257b>
  • Ciufolini Marco A., Canesi Sylvain, Ousmer Malika, Braun Norbert A.: Synthetic ventures inspired by biosynthetic hypotheses: the evolution of a method for the oxidative amidation of phenols. Tetrahedron 2006, 62, 5318. <http://dx.doi.org/10.1016/j.tet.2006.01.111>
  • Narasaka Koichi, Kitamura Mitsuru: Amination with Oximes. Eur J Org Chem 2005, 2005, 4505. <http://dx.doi.org/10.1002/ejoc.200500389>