One-pot synthesis of chromeno[2,3-b]isoindolo[1,2-e]pyrrole-12,13-dione derivatives by sequential reaction of ninhydrin, 2-aminochromen-4-ones and arylamines
Author:
Affiliation:
1. Department of Chemistry, R. K. Mission Vivekananda Centenary College, Rahara, Kolkata, West Bengal, India
Funder
Council of Scientific and Industrial Research
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2016.1170147
Reference15 articles.
1. Cyclization reactions of ninhydrin with aromatic amines and ureas
2. Synthesis of tetrahydroindeno[1,2-b]indol-10-ones and their rearrangement to [2]benzopyrano[4,3-b]indol-5-ones
3. Domino Reaction of 2,2-Dihydroxyindene-1,3-dione with Aromatic Amines: Efficient Synthesis of Isochromeno[4,3-b]indol-5(11H)-one Derivatives
4. Facile synthesis of substituted pyrrole-fused isocoumarins from ninhydrin
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2. [3+3] Annulation Reaction of 2‐Amino‐4 H ‐chromen‐4‐ones with Cinnamaldehydes or Aromatic Aldehydes and Ethanal in One Pot: Access to 2‐Aryl‐5 H ‐Chromeno[2,3‐ b ]pyridin‐5‐ones;Asian Journal of Organic Chemistry;2022-09-20
3. DBU-Mediated Domino Annulation Reaction of 2-Amino-4H-chromen-4-ones and Aromatic Aldehydes for Synthesis of Polysubstituted 3-Hydroxy-5H-chromeno[2,3-b]pyridinones;The Journal of Organic Chemistry;2022-08-12
4. Keggin-type heteropoly-11-molybdo-1-vanadophosphoric acid supported montmorillonite K-10 clay-catalysed one-pot multi-component synthesis of chromeno[2,3-b]indoles;Research on Chemical Intermediates;2021-05-11
5. Recent applications of ninhydrin in multicomponent reactions;RSC Advances;2020
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