The first synthesis of 6-(phenylethynyl)-substituted tetrahydroazocino[5,4-b]indoles

The reaction of 2-methyl-1-(phenylethynyl)-2,3,4,9-tetrahydro-1?-β-carboline with activated alkynes in acetonitrile led to the formation of 1-vinyl-substituted β-carbolines and condensed azocines. © 2016 Springer Science+Business Media New York.

Authors
Voskressensky L.G. 1 , Titov A.A. 1 , Kobzev M.S. 1 , Samavati R. 1 , Borisov R.S. 1 , Kulikova L.N. 1 , Varlamov A.V. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
1
Language
English
Pages
68-70
Status
Published
Link
External link
DOI
10.1007/s10593-016-1831-9
Volume
52
Year
2016
Organizations
  • 1 Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
Keywords
Acetylacetylene; Azocinoindoles; DMAD; Methylpropiolate; Vinyl-substituted β-carbolines; β-carbolines
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/4067/
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