Abstract: Angewandte Chemie International Edition in EnglishVolume 22, Issue 7 p. 543-543 Communication Thietones, Oxetones, and Azetones† Prof. Dr. Curt Wentrup, Corresponding Author Prof. Dr. Curt Wentrup Fachbereich Chemie der Universität Lahnberge, D-3550 Marburg (Germany)Fachbereich Chemie der Universität Lahnberge, D-3550 Marburg (Germany)Search for more papers by this authorGerhard Gross, Gerhard Gross Fachbereich Chemie der Universität Lahnberge, D-3550 Marburg (Germany)Search for more papers by this author Prof. Dr. Curt Wentrup, Corresponding Author Prof. Dr. Curt Wentrup Fachbereich Chemie der Universität Lahnberge, D-3550 Marburg (Germany)Fachbereich Chemie der Universität Lahnberge, D-3550 Marburg (Germany)Search for more papers by this authorGerhard Gross, Gerhard Gross Fachbereich Chemie der Universität Lahnberge, D-3550 Marburg (Germany)Search for more papers by this author First published: July 1983 https://doi.org/10.1002/anie.198305431Citations: 11 † This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. 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 2: IR: 1800 cm−1; MS: m/z 186 (M+); 1H-NMR (CDCl3, 400 MHz): δ=7.40 (t,J = 8Hz), 7.43 (s), 7.46 (s), 7.55 (t, J = 8 Hz), 7.67 (d, J = 8 Hz), 7.78 (d, J = 8 Hz); 13C-NMR (CDCl3, 100.6 MHz) (multiplicity, incl. long range couplings): δ=177.7 (s; C-2), 146.1 (s; C-2a), 138.3 (s; C-7a), 135.7 (s; C-3a), 131.4 (s; C-8a), 130.8 (dt), 129.6 (dd), 127.1 (dt), 125.9 (dd), 120.8 (dd), 118.9 (dd). 2 7: IR: 1793 cm−1; MS: m/z 186 (M+); 1H-NMR (CDCl3, 400 MHz, −40°C): δ = 7.38 (t, J = 8 Hz), 7.42 (d, J = 8 Hz), 7.56 (t, J = 8 Hz), 7.76 (d, J = 8 Hz), 7.80 (d, J = 8 Hz), 7.90 (d, J = 8 Hz). 3(a) O. L. Chapman, C. L. McIntosh, J. Am. Chem. Soc. 92 (1970) 7001; (b) R. Schulz, A. Schweig, Tetrahedron Lett. 1979, 59. 4 O. L. Chapman, C. L. McIntosh, J. Pacansky, G. V. Calder, G. Orr, J. Am. Chem. Soc. 95 (1973) 4061. 5 J. W. Airan, S. V. Shah, J. Indian Chem. Soc. 19 (1942) 333. Citing Literature Volume22, Issue7July 1983Pages 543-543 ReferencesRelatedInformation
Publication Year: 1983
Publication Date: 1983-07-01
Language: en
Type: article
Indexed In: ['crossref']
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Cited By Count: 22
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