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Stereoselective intramolecular cyclization to 4-(hydroxymethyl)-3-(1H-indolyl)oxazolidin-2-ones
Authors:Chiummiento Lucia  Funicello Maria  Tramutola Francesco
Affiliation:Dipartimento di Chimica A. M. Tamburro, Università degli Studi della Basilicata, Via dell'Ateneo Lucano 10, 85100, Potenza, Italy.
Abstract:A simple high-yield three-steps route to optically active 4-hydroxymethyl-3-(1H-indolyl)oxazolidin-2-ones from (S)-glycidol is described. The key intermediates (R)-oxiran-2-ylmethyl 1H-indol-4/-5-ylcarbamates are obtained in high yields from (S)-glycidol. These are readily transformed to oxazolidin-2-ones, very interesting building blocks in drug synthesis.
Keywords:heterocycles  building block  indolyloxazolidinones  antibacterial  organic synthesis
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