Unexpected synthesis of azepino[4,3,2- cd ]indoles from 4-aminoindoles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Biomedical Importance of Indoles
2. Total Synthesis of (−)-N-Methylwelwitindolinone C Isothiocyanate
3. A Synthesis of 1,3,4,5-Tetrahydropyrrolo[4,3,2-de]quinoline
4. Azepinoindoles. III. 3,4,5,6-Tetrahydro-1H-azepino[4,3,2,-cd]indoles
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1. A Synthetic Route to Tetrahydro-1H-azepino[4,3,2-cd]indoles via Ring-Opening Cyclization of Activated Azetidines with 4-Bromoindole: Toward a Vasopressin V2 Receptor Antagonist;The Journal of Organic Chemistry;2024-08-05
2. Fused Triazole-Azepine Hybrids as Potential Non-Steroidal Antiinflammatory Agents;Scientia Pharmaceutica;2023-05-16
3. Regioselectivity of the SEAr-based cyclizations and SEAr-terminated annulations of 3,5-unsubstituted, 4-substituted indoles;Beilstein Journal of Organic Chemistry;2022-03-08
4. Divergent synthesis of 4-amino indoles with free amine groups via tandem reaction of 2-alkynylanilines;Organic Chemistry Frontiers;2022
5. Water‐Promoted Synthesis of Azepino[3,4,5‐ cd ]indole Analogues via Pictet‐Spengler Reaction;ChemistrySelect;2020-04-20
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