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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.


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Synthesis of γ-Butyrolactones by a Baeye
✍ Ana Maria Faísca Phillips; Carlos Romão 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 211 KB 👁 1 views

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-