Regioselective [6π+2π] cycloaddition of 1,2-dienes to 7-substituted 1,3,5-cycloheptatrienes catalyzed by Ti(acac)2Cl2—Et2AlCl
- Autores: Kadikova G.N.1, Kolokoltsev D.I.1, Meshcheryakova E.S.1, D’yakonov V.A.1, Dzhemilev U.M.1
-
Afiliações:
- Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
- Edição: Volume 65, Nº 1 (2016)
- Páginas: 195-199
- Seção: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/236895
- DOI: https://doi.org/10.1007/s11172-016-1283-5
- ID: 236895
Citar
Resumo
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.
Sobre autores
G. Kadikova
Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
Email: DyakonovVA@gmail.com
Rússia, 141 prosp. Oktyabrya, Ufa, 450075
D. Kolokoltsev
Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
Email: DyakonovVA@gmail.com
Rússia, 141 prosp. Oktyabrya, Ufa, 450075
E. Meshcheryakova
Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
Email: DyakonovVA@gmail.com
Rússia, 141 prosp. Oktyabrya, Ufa, 450075
V. D’yakonov
Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
Autor responsável pela correspondência
Email: DyakonovVA@gmail.com
Rússia, 141 prosp. Oktyabrya, Ufa, 450075
U. Dzhemilev
Institute of Petrochemistry and Catalysis, Russian Academy of Sciences
Email: DyakonovVA@gmail.com
Rússia, 141 prosp. Oktyabrya, Ufa, 450075
Arquivos suplementares
