Portal de Periódicos da CAPES

Reaction of Metalated Nitrosamines with Nitriles. A New Method for Preparation of v ‐Triazoles

1972; Wiley; Volume: 11; Issue: 12 Linguagem: Inglês

10.1002/anie.197211021

1521-3773

Dieter Seebàch, Dieter Enders,

Chemical Synthesis and Analysis

Angewandte Chemie International Edition in EnglishVolume 11, Issue 12 p. 1102-1103 Communication Reaction of Metalated Nitrosamines with Nitriles. A New Method for Preparation of v-Triazoles† Prof. Dr. Dieter Seebach, Prof. Dr. Dieter Seebach Institut für Organische Chemie, Fachbereich Chemie der Universität, 63 Giessen, Ludwigstrasse 21 (Germany)Search for more papers by this authorDipl.-Chem. Dieter Enders, Corresponding Author Dipl.-Chem. Dieter Enders Institut für Organische Chemie, Fachbereich Chemie der Universität, 63 Giessen, Ludwigstrasse 21 (Germany)Institut für Organische Chemie, Fachbereich Chemie der Universität, 63 Giessen, Ludwigstrasse 21 (Germany)Search for more papers by this author Prof. Dr. Dieter Seebach, Prof. Dr. Dieter Seebach Institut für Organische Chemie, Fachbereich Chemie der Universität, 63 Giessen, Ludwigstrasse 21 (Germany)Search for more papers by this authorDipl.-Chem. Dieter Enders, Corresponding Author Dipl.-Chem. Dieter Enders Institut für Organische Chemie, Fachbereich Chemie der Universität, 63 Giessen, Ludwigstrasse 21 (Germany)Institut für Organische Chemie, Fachbereich Chemie der Universität, 63 Giessen, Ludwigstrasse 21 (Germany)Search for more papers by this author First published: December 1972 https://doi.org/10.1002/anie.197211021Citations: 18 † We thank the Deutsche Forschungsgemeinschaft for financial support. 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 No abstract is available for this article. References 1 D. Seebach and D. Enders, Angew. Chem. 84, 350, 1186 (1972); Angew. Chem. internat. Edit. 11, 301, 1101 (1972). 2 v-Triazoles have previously been prepared from: (a) 1,2-dicarbonyl compounds and hydrazines or hydroxylamine/hydrazines; (b) α-diazo carbonyl compounds and primary amines; (c) nitriles and diazo compounds; and (d) acetylenes and azides (the most important method): F. R. Benson and W. L. Savell, Chem. Rev. 46, 1 (1950). 3 H. Hoberg, Liebigs Ann. Chem. 707, 147 (1967). 4 C. W. Rees et al., Chem. Commun. 1971, 532, 1518, 1519. 5 For example, acetonitrile gives no triazole on treatment with lithiated dimethylnitrosamine. Citing Literature Volume11, Issue12December 1972Pages 1102-1103 ReferencesRelatedInformation