Direct synthesis of N-functionalized indoles through isomerization of azomethine ylides.
Org Biomol Chem
; 22(4): 741-744, 2024 Jan 24.
Article
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| MEDLINE
| ID: mdl-38170630
ABSTRACT
An unexpected isomerization of azomethine ylides generated in situ from isatin with indoline-2-carboxylic acid has been disclosed, providing direct access to N-functionalized indole scaffolds. This protocol has good functional group tolerance and provides various 3-(1H-indol-1-yl)indolin-2-one derivatives in moderate to high yields simply by using alcohol as the solvent, with no additional additive being required.
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MEDLINE
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Org Biomol Chem
Asunto de la revista:
BIOQUIMICA
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QUIMICA
Año:
2024
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Article