Selective Hydrogenations of 1,1‐Disubstituted Cyclopropanes
1976; Wiley; Volume: 15; Issue: 6 Linguagem: Inglês
10.1002/anie.197603731
ISSN1521-3773
Autores Tópico(s)Catalytic Alkyne Reactions
ResumoAngewandte Chemie International Edition in EnglishVolume 15, Issue 6 p. 373-374 Communication Selective Hydrogenations of 1,1-Disubstituted Cyclopropanes† Dipl.-Chem. Claus Gröger, Dipl.-Chem. Claus Gröger Institut für Anorganische Chemie FB21-WE1 der Freien Universität Richard-Willstätter-Allee, 7500 Karlsruhe 1 (Germany)Search for more papers by this authorProf. Dr. Hans Musso, Corresponding Author Prof. Dr. Hans Musso Institut für Anorganische Chemie FB21-WE1 der Freien Universität Richard-Willstätter-Allee, 7500 Karlsruhe 1 (Germany)Institut für Anorganische Chemie FB21-WE1 der Freien Universität Richard-Willstätter-Allee, 7500 Karlsruhe 1 (Germany)Search for more papers by this author Dipl.-Chem. Claus Gröger, Dipl.-Chem. Claus Gröger Institut für Anorganische Chemie FB21-WE1 der Freien Universität Richard-Willstätter-Allee, 7500 Karlsruhe 1 (Germany)Search for more papers by this authorProf. Dr. Hans Musso, Corresponding Author Prof. Dr. Hans Musso Institut für Anorganische Chemie FB21-WE1 der Freien Universität Richard-Willstätter-Allee, 7500 Karlsruhe 1 (Germany)Institut für Anorganische Chemie FB21-WE1 der Freien Universität Richard-Willstätter-Allee, 7500 Karlsruhe 1 (Germany)Search for more papers by this author First published: June 1976 https://doi.org/10.1002/anie.197603731Citations: 17 † Hydrogenolysis of Small Ring Compounds, Part 4. This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. All new compounds gave correct elemental analyses and spectra.—Part 3: ref. [1]. 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 B. Deppisch, H. Guth, H. Musso, and E. Ōsawa, Chem. Ber. 109 (1976), in press. 2 R. Hoffmann, Tetrahedron Lett. 1970, 2907; H. Günther, Tetrahedron Lett. 1970, 5173; F. G. Klärner, Tetrahedron Lett. 1974, 19; R. Hoffmann and W. D. Stohrer, J. Am. Chem. Soc. 93, 6941 (1971); A. H. Andrist, J. Am. Chem. Soc. 95, 7531 (1973). 3 10 % Palladium on charcoal: Merck Darmstadt. PtO2: Degussa, Hanau. 4 (3a), (3b), and (2f): NMR <1%; (2c), (2d), (2e) not detectable in VPC <0.1%. 5 D. J. Brown and K. Ienega, J. Chem. Soc. Perkin 1, 1974, 373; H. U. Sieveking and W. Lüttke, Angew. Chem. 81, 431 (1969); Angew. Chem. Int. Ed. Engl. 8, 458 (1969). 6Summary: J. Newham, Chem. Rev. 63, 123 (1963). 7 P. v. R. Schleyer, W. Buss, J. C. Martin, and B. R. Ree, J. Am. Chem. Soc. 91, 5880, 5882 (1969). 8 N. S. Nametkin, V. M. Vdorin, E. S. Finkelstein, and A. M. Popov, Dokl. Akad. Nauk SSSR, Ser. Khim. 205, 630 (1972); Izv. Akad. Nauk SSSR, Ser. Khim. 1973, 2806. 9 P. Lindberg, R. Bergmann, and B. Wickberg, J. Chem. Soc. Chem. Commun. 1975, 946. 10 W. Cocker, P. V. R. Shannon, and P. A. Staniland, Chem. Commun. 1965, 254. 11 H. Musso, Chem. Ber. 101, 3710 (1968). 12 K. J. Stahl and H. Musso, to be published. Citing Literature Volume15, Issue6June 1976Pages 373-374 ReferencesRelatedInformation
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