Regioselective [6π+2π] cycloaddition of 1,2-dienes to 7-substituted 1,3,5-cycloheptatrienes catalyzed by Ti(acac)2Cl2—Et2AlCl
- Authors: Kadikova G.N.1, Kolokoltsev D.I.1, Meshcheryakova E.S.1, D’yakonov V.A.1, Dzhemilev U.M.1
-
Affiliations:
- Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
- Issue: Vol 65, No 1 (2016)
- Pages: 195-199
- Section: Full Articles
- URL: https://journal-vniispk.ru/1066-5285/article/view/236895
- DOI: https://doi.org/10.1007/s11172-016-1283-5
- ID: 236895
Cite item
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
Supplementary files
