4.4 Article

Facile synthesis of fluorine-containing 1,10-phenanthrolines by the pyridine-ring formation reaction of N-propargyl-5,7-bis(trifluoroacetyl)-8-quinolylamine with amines: isolation of the intermediates 1,4-dihydro-1,10-phenanthrolin-4-ols

期刊

TETRAHEDRON LETTERS
卷 49, 期 50, 页码 7161-7164

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2008.09.172

关键词

1,10-Phenanthrolines; Fluorine; Pyridine-ring formation; Propargylamines; 8-Quinolylamines

资金

  1. Japan Society for the Promotion of Science (JSPS)
  2. Centre National de la Recherche Scientifique (CNRS)
  3. Direction des Relations Internationales (DRI)

向作者/读者索取更多资源

Novel fluorine-containing 1,10-phenanthrolines having dialkyl-, alkyl, and arylaminomethyl substituents at the 3-position were easily synthesized in moderate yields by the pyridine-ring formation reaction of N-propargyl-5,7-bis(trifluoroacetyl)-8-quinolylamine with various a mines. Unexpectedly, the reactive intermediates 1,4-dihydro-1,10-phenanthrolin-4-ols were isolated for the first time in the reactions with dialkylamines. (C) 2008 Elsevier Ltd. All rights reserved.

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