Artigo Revisado por pares

Simple Synthesis of Dicyclopropylidenemethane

1975; Wiley; Volume: 14; Issue: 12 Linguagem: Inglês

10.1002/anie.197508212

ISSN

1521-3773

Autores

Richard Kopp, Michael Hanack,

Tópico(s)

Synthetic Organic Chemistry Methods

Resumo

Angewandte Chemie International Edition in EnglishVolume 14, Issue 12 p. 821-822 Communication Simple Synthesis of Dicyclopropylidenemethane† Dipl.-Chem. Richard Kopp, Dipl.-Chem. Richard Kopp Institut für Organische Chemie der Universität, 74 Tübingen 1, Auf der Morgenstelle 18 (Germany)Search for more papers by this authorProf. Dr. Michael Hanack, Corresponding Author Prof. Dr. Michael Hanack Institut für Organische Chemie der Universität, 74 Tübingen 1, Auf der Morgenstelle 18 (Germany)Institut für Organische Chemie der Universität, 74 Tübingen 1, Auf der Morgenstelle 18 (Germany)Search for more papers by this author Dipl.-Chem. Richard Kopp, Dipl.-Chem. Richard Kopp Institut für Organische Chemie der Universität, 74 Tübingen 1, Auf der Morgenstelle 18 (Germany)Search for more papers by this authorProf. Dr. Michael Hanack, Corresponding Author Prof. Dr. Michael Hanack Institut für Organische Chemie der Universität, 74 Tübingen 1, Auf der Morgenstelle 18 (Germany)Institut für Organische Chemie der Universität, 74 Tübingen 1, Auf der Morgenstelle 18 (Germany)Search for more papers by this author First published: December 1975 https://doi.org/10.1002/anie.197508212Citations: 4 † This work was supported by 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 H. U. Siehl, J. C. Carnahan, jr., L. Eckes, and M. Hanack, Angew. Chem. 86, 677 (1974); 10.1002/ange.19740861813 CASGoogle Scholar Angew. Chem. internat. Edit. 13, 675 (1974). 10.1002/anie.197406751 Web of Science®Google Scholar 2 L. Fitjer and J. M. Conia, Angew. Chem. 85, 832 (1973); 10.1002/ange.19730851819 CASGoogle Scholar Angew. Chem. internat. Edit. 12, 761 (1973). 10.1002/anie.197307611 Web of Science®Google Scholar 3 K. Utimoto, M. Tamura, and K. Sisido, Tetrahedron 29, 1169 (1973). 10.1016/0040-4020(73)80096-1 CASWeb of Science®Google Scholar 4 L. B. Young and W. S. Trahanovsky, J. Org. Chem. 32, 2349 (1967); 10.1021/jo01282a058 CASWeb of Science®Google Scholar J. P. Barnier, J. M. Denis, J. Salaün, and J. M. Conia, Tetrahedron 30, 1392 (1974). Google Scholar 5 M. Hanack, T. Bässler, W. Eymann, W. E. Heyd, and R. Kopp, J. Am. Chem. Soc. 96, 6686 (1974). 10.1021/ja00828a024 CASWeb of Science®Google Scholar Citing Literature Volume14, Issue12December 1975Pages 821-822 ReferencesRelatedInformation

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