Please use this identifier to cite or link to this item:
http://hdl.handle.net/2445/167518
Title: | Enantioselective Synthesis of Spiro[indolizidine-1,3 '-oxindoles] |
Author: | Pérez Bosch, Maria Ramos, Carlos Massi, Lucia Gazzola, Silvia Taglienti, Chiara Yayik, Nihan Molins i Grau, Elies Viayna Gaza, Antonio Luque Garriga, F. Xavier Bosch Cartes, Joan Amat Tusón, Mercedes |
Keywords: | Síntesi orgànica Enantiòmers Oxidació Compostos heterocíclics Organic synthesis Enantiomers Oxidation Heterocyclic compounds |
Issue Date: | 4-Aug-2017 |
Publisher: | American Chemical Society |
Abstract: | A three-step procedure for the enantioselective synthesis of spiro[indolizidine-1,3'-oxindoles], consisting of a stereoselective cyclocondensation reaction between (S)-tryptophanol and a prochiral or racemic 5-oxoester, bromination of the resulting oxazolopiperidone lactam, and a final stereoselective spirocyclization, is reported. |
Note: | Versió postprint del document publicat a: https://doi.org/10.1021/acs.orglett.71301818 |
It is part of: | Organic Letters, 2017, vol. 19, num. 15, p. 4050-4053 |
URI: | http://hdl.handle.net/2445/167518 |
Related resource: | https://doi.org/10.1021/acs.orglett.71301818 |
ISSN: | 1523-7060 |
Appears in Collections: | Articles publicats en revistes (Institut de Biomedicina (IBUB)) Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia) |
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