2014
DOI: 10.1007/s00706-014-1216-7
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Microwave-assisted synthesis of fused tricyclic pyrazino[1,2-a]indole derivatives

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Cited by 8 publications
(2 citation statements)
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“…Regarding natural occurrence, secondary metabolites of marine flora and fauna exhibiting antibacterial and antiproliferative activities incorporate pyrazino­[1,2- a ]­indole and methoxy­pyrazine moieties (Figure ). The aforementioned properties render pyrazino­indoles an interesting synthesis target . Recent synthesis examples include alkyne hydroamination, a two-step Ugi–alkyne hydroamination reaction sequence, and bromo­lactamization of N -allylindole-2-carbamide .…”
Section: Introductionmentioning
confidence: 99%
“…Regarding natural occurrence, secondary metabolites of marine flora and fauna exhibiting antibacterial and antiproliferative activities incorporate pyrazino­[1,2- a ]­indole and methoxy­pyrazine moieties (Figure ). The aforementioned properties render pyrazino­indoles an interesting synthesis target . Recent synthesis examples include alkyne hydroamination, a two-step Ugi–alkyne hydroamination reaction sequence, and bromo­lactamization of N -allylindole-2-carbamide .…”
Section: Introductionmentioning
confidence: 99%
“…In spite of the efficacy of pyrazino [1,2a]indoles, literature lacks adequate reports for their synthesis. [20][21][22][23][24] Hence, development of novel, efficient, easy, and rapid synthetic approaches is still a common research area. Intramolecular cyclization of several 2-carbonyl-1propargylindoles in the presence of ammonia was developed by Abbiati et al 20 The reaction was investigated in various heating conditions in the presence of different metal catalysts.…”
Section: Introductionmentioning
confidence: 99%