Journal
CHEMISTRY LETTERS
Volume 51, Issue 11, Pages 1067-1069Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.220368
Keywords
Anodic oxidation; Indirect electrolysis; Indole
Categories
Funding
- JSPS KAKENHI [22K05115, 22H02122]
- Ministry of Education, Culture, Sports, Science & Technology, Japan [20K22534, 21A204]
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The semi-pinacol rearrangement of tetrahydro-P-carbolines to afford 3-spirooxindoles was efficiently promoted by anodically generated bromonium ion equivalent as a halogen mediator.
The semi-pinacol rearrangement of tetrahydro-P-carbolines afforded 3-spirooxindoles. The anodically generated bromonium ion equivalent as a halogen mediator efficiently promoted the transformation.
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