Recently vinyl selenones have been discovered as excellent substrates to synthesize indole derivatives in an cost-inexpensive and eco-friendly reaction. Herein we describe the synthesis of 3,4-dihydropyrazino[1,2-a]indol-1(2H)-ones, which attracted the attention of medicinal chemists thanks to their important biological activities such as antifungal, antihistaminergic and anti-serotoninergic. The reaction takes place via a Michael addition-cyclization cascade starting from vinyl selenones and (1H-indol-2yl)carboxamides using as base potassium hydroxide.

Synthesis of 3,4-Dihydropyrazino[1,2-a]indol-1(2H)-Ones by Cascade Addition-Cyclization Reactions from Vinyl Selenones

SANCINETO, LUCA;MARINI, Francesca;SANTI, Claudio;BAGNOLI, Luana
2014

Abstract

Recently vinyl selenones have been discovered as excellent substrates to synthesize indole derivatives in an cost-inexpensive and eco-friendly reaction. Herein we describe the synthesis of 3,4-dihydropyrazino[1,2-a]indol-1(2H)-ones, which attracted the attention of medicinal chemists thanks to their important biological activities such as antifungal, antihistaminergic and anti-serotoninergic. The reaction takes place via a Michael addition-cyclization cascade starting from vinyl selenones and (1H-indol-2yl)carboxamides using as base potassium hydroxide.
2014
978-3-906980-55-3
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1287952
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