Novel domino reaction of N-(cyanomethyl)-5,10-dihydro[1]benzosilano[3,2-c] pyridinium salts with salicylaldehydes

The synthesis of benzosilanochromenoimidazopyridines was accomplished by a domino reaction of 5,5-dimethyl-10-oxo- and 10-hydroxy-10- allyldihydrobenzosilanopyridinium N-cyanomethyl salts with salicyl- and 5-bromosalicylaldehydes. It was found that in the case of the 10-allyl-10-hydroxy-dihydrobenzosilanopyridinium salts the reaction occurred at both α-positions of the pyridine fragment to form a mixture of the isomeric benzosilano[3,2-c]- and benzosilano[2,3-d]chromenoimidazo-pyridines. © 2013 Springer Science+Business Media New York.

Authors
Voskressensky L.G. 1 , Sokolova E.A. 1 , Festa A.A. 1 , Khrustalev V.N.2 , Van Tuyen N. , Anh L.T.4 , Varlamov A.V. 1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
3
Language
English
Pages
484-490
Status
Published
Volume
49
Year
2013
Organizations
  • 1 Peoples Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow 117198, Russian Federation
  • 2 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov St., Moscow 119991, Russian Federation
  • 3 Chemistry Institute, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet St., Cau Giay Hanoi, Viet Nam
  • 4 Chemistry Faculty, Vietnam National Science University, 144 Ksan Tui St., Cau Giay Hanoi, Viet Nam
Keywords
benzosilanopyridine; domino reaction; salicylaldehyde
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/2065/
Share

Other records