Volume 9, Issue 11 p. 3099-3101
Communication

Reaction of a Dialumene‐Benzene Adduct with Diphenylacetylene: Formation of 3,4‐Dialuminacyclobutene and 5,6‐Dialuminabicyclo[2.1.1]hex‐2‐ene Derivatives

Dr. Tomohiro Agou

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

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Koichi Nagata

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

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Prof. Dr. Takahiro Sasamori

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

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Prof. Dr. Norihiro Tokitoh

Corresponding Author

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209Search for more papers by this author
First published: 22 August 2014
Citations: 10

Abstract

Reaction of a dialumene‐benzene adduct bearing bulky aryl substituents with diphenylacetylene was found to give a novel 5,6‐dialuminabicyclo[2.1.1]hex‐2‐ene derivative in addition to the 3,4‐dialuminacyclobutene derivative, the formal [2+2]cycloadduct of an intermediary dialumene with diphenylacetylene. The molecular structure of the newly obtained 5,6‐dialuminabicyclo[2.1.1]hex‐2‐ene has been elucidated by X‐ray crystallographic analysis.

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