A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, G. S. Borodkin, A. I. Klimenko, “Reaction of 2-methyl-3,4-dihydro-β-carbolin-2-ium iodide with acylmethyl halides controlled by electronic effects: a new route to 1,2-dihydroazepino[4,5-<i>b</i>]indoles”, Mendeleev Commun., 2018, Volume 28, Issue 1,Pages <nobr>83

This article is cited in 7 papers

Communications

Reaction of 2-methyl-3,4-dihydro-β-carbolin-2-ium iodide with acylmethyl halides controlled by electronic effects: a new route to 1,2-dihydroazepino[4,5-b]indoles

A. A. Zubenko^a, A. S. Morkovnik^b, L. N. Divaeva^b, V. G. Kartsev^c, G. S. Borodkin^b, A. I. Klimenko^d

^a North-Caucasian Zonal Research Veterinary Institute, Novocherkassk, Russian Federation
^b Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
^c 'InterBioScreen Ltd.', Chernogolovka, Moscow Region, Russian Federation
^d Don State Agrarian University, Novocherkassk, Russian Federation

Abstract: 2-Methyl-3,4-dihydro-β-carbolin-2-ium iodide in the reaction with aryl halomethyl ketones is converted into 4- or/and 5-acyl-1,2-dihydroazepino[4,5-b]indoles depending on the electron donating effect of substituents in the aryl moiety of the halomethyl ketone.

Language: English

DOI: 10.1016/j.mencom.2018.01.028

	*Supplementary materials:*
		Supplementary_data_1.pdf	315.7 Kb