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Communication | Special issue | Vol 59, No. 1, 2003, pp.47-50
Published online, 1st January, 1970
DOI: 10.3987/COM-02-S8
High-pressure Cycloaddition Reaction of 1,3-Diphenylisobenzofuran with 6,6-Diphenylfulvene

Kanji Kubo,* Katsuji Hirowatari, Nobuo Kato, and Akira Mori*

*Instituete of Advanced Material Study, Kyushu University, 6-1, Kasuga-koen, Kasuga 816-8580, Japan

Abstract

High-pressure cycloaddition reaction of 1,3-diphenylisobenzofuran with 6,6-diphenylfulvene gave exo- and endo-[4+2]π cycloadducts in 29 and 20% yields, respectively. The structures of exo- and endo-[4+2]π cycloadducts were elucidated by X-Ray crystallographic analysis, the latter of which included a benzene molecule.