Open Access Open Access  Restricted Access Subscription Access

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

Леонид Г. Воскресенский, Александр А. Титов, Максим С. Кобзев, Реза Самавати, Роман С. Борисов, Лариса Н. Куликова, Алексей В. Варламов
Cover Image

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

 


Keywords


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

Full Text: PDF (Russian) Supplementary File(s): None


 

 

Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv