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1,3‐Dipolar Addition of Cyclic Diazo Ketones to Alkynes and Cyclopropene. Synthesis of Heterocycles by [1,5]‐Acyl Migration

1973; Wiley; Volume: 12; Issue: 3 Linguagem: Inglês

10.1002/anie.197302401

1521-3773

M. FRANCK‐NEUMANN, Christiane Buchecker,

Synthesis and Biological Evaluation

Angewandte Chemie International Edition in EnglishVolume 12, Issue 3 p. 240-241 Communication 1,3-Dipolar Addition of Cyclic Diazo Ketones to Alkynes and Cyclopropene. Synthesis of Heterocycles by [1,5]-Acyl Migration† Dr. Michel Franck-Neumann, Dr. Michel Franck-Neumann Laboratoire Associé au CNRS n° 31, Institut de Chimie de l'Université Louis Pasteur l, rue Blaise Pascal, F-67 Strasbourg (France)Search for more papers by this authorDr. Christiane Buchecker, Corresponding Author Dr. Christiane Buchecker Laboratoire Associé au CNRS n° 31, Institut de Chimie de l'Université Louis Pasteur l, rue Blaise Pascal, F-67 Strasbourg (France)Laboratoire Associé au CNRS no31, Institut de Chimie de l'Université Louis Pasteur l, rue Blaise Pascal, F-67 Strasbourg (France)Search for more papers by this author Dr. Michel Franck-Neumann, Dr. Michel Franck-Neumann Laboratoire Associé au CNRS n° 31, Institut de Chimie de l'Université Louis Pasteur l, rue Blaise Pascal, F-67 Strasbourg (France)Search for more papers by this authorDr. Christiane Buchecker, Corresponding Author Dr. Christiane Buchecker Laboratoire Associé au CNRS n° 31, Institut de Chimie de l'Université Louis Pasteur l, rue Blaise Pascal, F-67 Strasbourg (France)Laboratoire Associé au CNRS no31, Institut de Chimie de l'Université Louis Pasteur l, rue Blaise Pascal, F-67 Strasbourg (France)Search for more papers by this author First published: March 1973 https://doi.org/10.1002/anie.197302401Citations: 20 † Dedicated to Professor Rudolf Criegee on the occasion of his 70th birthday AboutPDF 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 No abstract is available for this article. References 1 M. Franck-Neumann and C. Buchecker, Tetrahedron Lett. 1972, 937. Google Scholar 2 M. Regitz and J. Rüter, Chem. Ber. 101, 1263 (1968). 10.1002/cber.19681010419 CASWeb of Science®Google Scholar 3 K. B. Wiberg, B. R. Lowry, and T. H. Colby, J. Amer. Chem. Soc. 83, 3998 (1961). 10.1021/ja01480a013 Google Scholar 4 M. O. Forster, J. Chem. Soc. 107, 260 (1915). 10.1039/ct9150700260 CASWeb of Science®Google Scholar 5 M. P. Cava, P. M. Weintraub, and E. J. Glamkowski, J. Org. Chem. 31, 2015 (1966); 10.1021/jo01344a533 CASPubMedWeb of Science®Google Scholar M. Avaro and J. Levisalles, Bull. Soc. Chim. France 1969, 3169. Google Scholar 6 M. Franck-Neumann and C. Buchecker, Tetrahedron Lett. 1969, 2659. Google Scholar 7 M. Franck-Neumann and C. Buchecker, Tetrahedron Lett. 1969, 15. Google Scholar Citing Literature Volume12, Issue3March 1973Pages 240-241 ReferencesRelatedInformation