Regioselective [6π+2π] cycloaddition of 1,2-dienes to 7-substituted 1,3,5-cycloheptatrienes catalyzed by Ti(acac)2Cl2—Et2AlCl


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Abstract

A reaction of 7-alkyl-, 7-allyl-, 7-phenyl-1,3,5-cycloheptatrienes with 1,2-dienes in the presence of the two-component catalytic system Ti(acac)2Cl2—Et2AlCl, which led to the formation of practically important substituted endo-bicyclo[4.2.1]nona-2,4-dienes in up to 90% yields, was accomplished for the first time.

About the authors

G. N. Kadikova

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: DyakonovVA@gmail.com
Russian Federation, 141 prosp. Oktyabrya, Ufa, 450075

D. I. Kolokoltsev

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: DyakonovVA@gmail.com
Russian Federation, 141 prosp. Oktyabrya, Ufa, 450075

E. S. Meshcheryakova

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: DyakonovVA@gmail.com
Russian Federation, 141 prosp. Oktyabrya, Ufa, 450075

V. A. D’yakonov

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Author for correspondence.
Email: DyakonovVA@gmail.com
Russian Federation, 141 prosp. Oktyabrya, Ufa, 450075

U. M. Dzhemilev

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: DyakonovVA@gmail.com
Russian Federation, 141 prosp. Oktyabrya, Ufa, 450075

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