A concise synthesis of 3-hydroxyindole-2-carboxylates by a modified Baeyer–Villiger oxidation
✍ Scribed by Zachary L. Hickman; Claudio F. Sturino; Nicolas Lachance
- Book ID
- 104211007
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 87 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Indole-2-carboxylates are converted in good yields to 3-hydroxyindole-2-carboxylates by use of a Vilsmeier-Haack/Baeyer-Villiger reaction sequence. A systematic examination of the various indole substituents revealed this route to be general in scope.
📜 SIMILAR VOLUMES
Baeyer-Villiger reaction / Lactones / Methyltrioxorhenium / Catalysis / Oxidations / Cyclobutanones / Ketones γ-Butyrolactones were obtained in good yields and high rings, and chlorine substituents. A trimethylsiloxysubstituted ketone was converted directly into a hydro-regioselectivity by a Baeyer-