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- W2084872910 abstract "Journal of Heterocyclic ChemistryVolume 12, Issue 2 p. 379-383 Note Some formylation reactions of imidazo[1,5-a] pyridine and pyrrocoline Omar Fuentes, Omar Fuentes Department of Chemistry, The University of Alabama, University, Alabama 35486Search for more papers by this authorWilliam W. Paudler, William W. Paudler Department of Chemistry, The University of Alabama, University, Alabama 35486Search for more papers by this author Omar Fuentes, Omar Fuentes Department of Chemistry, The University of Alabama, University, Alabama 35486Search for more papers by this authorWilliam W. Paudler, William W. Paudler Department of Chemistry, The University of Alabama, University, Alabama 35486Search for more papers by this author First published: April 1975 https://doi.org/10.1002/jhet.5570120235Citations: 27AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 O. Fuentes and W. W. Paudler, J. Org. Chem., in press (1975). 2 J. D. Bower and G. L. Ramage, J. Chem. Soc., 2834 (1955). 3 Pmr analysis of the crude reaction mixture showed the presence of the 1 and 3-formyl derivatives in a ratio of 2.6:1. 4 V. Boekelheide and J. R. Wingassen, J. Am. Chem. Soc., 81, 1456 (1959). 5 Pmr analysis showed the presence of the 1 and 3-formyl derivatives in a ratio of 1.0:4.5. 6 Pmr analysis showed the presence of the 3- and 1-nitroso derivatives in a tatio of 4.8:1.0. 7 D. E. Ames, R. F. Grey and W. A. Jones, J. Chem. Soc., 620 (1959), and references therein. 8 N. P. Buu-Hoi, N. Hoan and R. Royar, Bull. Soc. Chim. France, 489 (1950). 9 W. W. Paudler and L. S. Helmick, J. Org. Chem., 33, 1087 (1968). 10 The authors are aware of the dangers involved in using ground-state electron density distribution to reaction intermediates. However, in most heterocyclic systems this argument is acceptable because of rather minor changes involved in formation of the transition states. 11 W. W. Paudler and J. E. Kuder, J. Org. Chem., 32, 2430 (1967). Citing Literature Volume12, Issue2April 1975Pages 379-383 ReferencesRelatedInformation" @default.
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- W2084872910 title "Some formylation reactions of imidazo[1,5-<i>a</i>] pyridine and pyrrocoline" @default.
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