THE FIRST SYNTHESIS OF 6-(PHENYLETHYNYL)-SUBSTITUTED TETRAHYDROAZOCINO[5,4-<i>b</i>]INDOLES

Authors

  • Леонид Г. Воскресенский Peoples Friendship University of Russia
  • Александр А. Титов Peoples' Friendship University of Russia
  • Максим С. Кобзев Peoples' Friendship University of Russia
  • Реза Самавати Peoples' Friendship University of Russia
  • Роман С. Борисов Peoples' Friendship University of Russia
  • Лариса Н. Куликова Peoples' Friendship University of Russia
  • Алексей В. Варламов Peoples' Friendship University of Russia

DOI:

https://doi.org/10.1007/2825

Keywords:

acetylacetylene, azocinoindoles, β-carbolines, DMAD, methylpropiolate, vinyl-substituted β-carbolin

Abstract

The reaction of 2-methyl-1-(phenylethynyl)-2,3,4,9-tetrahydro-1Н-β-carboline with activated alkynes in acetonitrile led to the formation of 1-vinyl-substituted β-carbolines and condensed azocines.

How to Cite
Voskressensky, L. G.; Titov, A. A.; Kobzev, M. S.; Samavati, R.; Borisov, R. S.; Kulikova, L. N.; Varlamov, A. V. Chem. Heterocycl. Compd. 2016, 52, 68. [Khim. Geterotsikl. Soedin. 2016, 52, 68.]

For this article in the English edition see DOI 10.1007/s10593-016-1831-9

 

Author Biography

Леонид Г. Воскресенский, Peoples Friendship University of Russia

Organic Chemistry Department, professor

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Published

2016-01-27

Issue

Vol. 52 No. 1 (2016)

Section

Letters to the Editor