Volume 35, Issue 16 pp. 1843-1845
Communication
Full Access

An Unprecedented Biradical Cyclization as an Alternative Pathway to the Myers–Saito Cycloaromatization in the Thermal Reactions of Enyne Allenes

Prof. Dr. Michael Schmittel

Corresponding Author

Prof. Dr. Michael Schmittel

Institut für Organische Chemie der Universität, Am Hubland, D-97074 Würzburg (Germany) Fax: Int. code +(931) 888-4606 e-mail: [email protected]

Institut für Organische Chemie der Universität, Am Hubland, D-97074 Würzburg (Germany) Fax: Int. code +(931) 888-4606 e-mail: [email protected]Search for more papers by this author
Dipl.-Chem. Marc Strittmatter

Dipl.-Chem. Marc Strittmatter

Institut für Organische Chemie der Universität, Am Hubland, D-97074 Würzburg (Germany) Fax: Int. code +(931) 888-4606 e-mail: [email protected]

Search for more papers by this author
Dipl.-Chem. Susanne Kiau

Dipl.-Chem. Susanne Kiau

Institut für Organische Chemie der Universität, Am Hubland, D-97074 Würzburg (Germany) Fax: Int. code +(931) 888-4606 e-mail: [email protected]

Search for more papers by this author
First published: September 6, 1996
Citations: 82

Thermal and Electron Transfer Induced Reactions of Enediynes and Enyne Allenes, Part 4. Financial support from the Volkswagen-Stiftung and the Fonds der Chemischen Industrie is gratefully acknowledged. We thank Prof. Dr. C. Rüchardt and E. Hickl (Freiburg) for their kind help with the DSC experiments. Part 3: [6].

Dedicated to Professor Horst Prinzbach on the occasion of his 65th birthday

Graphical Abstract

Tales of the Unexpected. The thermal reaction of aryl-substituted enyne allenes 1 does not proceed by the expected Myers-Saito cycloaromatization. Instead a novel cyclization via intermediate benzofulvene biradicals 2 takes place.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.