Synthesis and structure of bicyclic enediynes via twofold carbenoid ring closure

Koenig, Burkhard and Pitsch, Wolfgang and Dix, Ina and Jones, Peter G. (2001) Synthesis and structure of bicyclic enediynes via twofold carbenoid ring closure. NEW JOURNAL OF CHEMISTRY, 25 (7). pp. 912-916. ISSN 1144-0546

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Abstract

Macrobicyclic enediynes were obtained in four steps from dicarboxylic diesters. The key step of the synthesis is a twofold carbenoid ring closing procedure from acyclic precursors. Crystal structure analyses showed that bicyclo[6.6.4]dienetetrayne is not strained. Thermal analysis revealed its low thermal reactivity. An attempt to obtain bicyclo[6.6.2]dienetetrayne structures using the same method failed.

Item Type: Article
Uncontrolled Keywords: ;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Depositing User: Dr. Gernot Deinzer
Date Deposited: 07 Mar 2022 10:29
Last Modified: 07 Mar 2022 10:29
URI: https://pred.uni-regensburg.de/id/eprint/41923

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