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Tetraasterane, Pentacyclo[6.4.0.0 2,7 .0 4,11 .0 5,10 ]dodecane

1975; Wiley; Volume: 14; Issue: 3 Linguagem: Romeno

10.1002/anie.197501801

1521-3773

Hans‐Martin Hutmacher, Hans‐Günter Fritz, Hans Musso,

Chemical Synthesis and Analysis

Angewandte Chemie International Edition in EnglishVolume 14, Issue 3 p. 180-181 Communication Tetraasterane, Pentacyclo[6.4.0.02,7.04,11.05,10]dodecane†‡ Dr. Hans-Martin Hutmacher, Dr. Hans-Martin Hutmacher Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Search for more papers by this authorDr. Hans-Günter Fritz, Dr. Hans-Günter Fritz Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Search for more papers by this authorProf. Dr. Hans Musso, Corresponding Author Prof. Dr. Hans Musso Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Search for more papers by this author Dr. Hans-Martin Hutmacher, Dr. Hans-Martin Hutmacher Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Search for more papers by this authorDr. Hans-Günter Fritz, Dr. Hans-Günter Fritz Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Search for more papers by this authorProf. Dr. Hans Musso, Corresponding Author Prof. Dr. Hans Musso Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Institut für Organische Chemie der Universität 75 Karlsruhe, Richard-Willstätter-Allee (Germany)Search for more papers by this author First published: March 1975 https://doi.org/10.1002/anie.197501801Citations: 20 † Asteranes, Part 12.—Part 11: see ref. [5]. ‡ This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. We are indebted to Dr. U. I. Záhorszky and Miss I. Gerhardt for recording numerous spectra. 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 Asteranes, Part 12.—Part 11: see ref. [5]. 2 R. C. Cookson, D. A. Cox, and J. Hudec, J. Chem. Soc. 1961, 4499; H. Hopf and H. Musso, Chem. Ber. 106, 143 (1973). 3 U. Biethan, U. v. Gizycki, and H. Musso, Tetrahedron Lett. 1965, 1477; U. Biethan and H. Musso, Chem. Ber. 100, 119 (1967). 4 J. P. Chesick, J. D. Dunitz, U. v. Gizycki, and H. Musso, Chem. Ber. 106, 150 (1973). 5 H.-G. Fritz, H. Henke, and H. Musso, Chem. Ber. 107, 3164 (1974). 6 G. Ahlgren, B. Åkermack, and R. Karlson, Acta Chem. Scand, 25, 753 (1971); G. Ahlgren and B. Åkermark, Tetrahedron Lett. 1973, 987; H.-G. Fritz, Dissertation, Universität Karlsruhe 1972. 7 K. B. Becker, M. Geisel, C. A. Grob, and F. Kuhnen, Synthesis 1973, 493. 8 Based on 35Cl337Cl. Citing Literature Volume14, Issue3March 1975Pages 180-181 ReferencesRelatedInformation