dc.contributor.author
Pérez Bosch, Maria
dc.contributor.author
Ramos, Carlos
dc.contributor.author
Massi, Lucia
dc.contributor.author
Gazzola, Silvia
dc.contributor.author
Taglienti, Chiara
dc.contributor.author
Yayik, Nihan
dc.contributor.author
Molins i Grau, Elies
dc.contributor.author
Viayna Gaza, Antonio
dc.contributor.author
Luque Garriga, F. Xavier
dc.contributor.author
Bosch Cartes, Joan
dc.contributor.author
Amat Tusón, Mercedes
dc.date.issued
2020-07-03T11:08:04Z
dc.date.issued
2020-07-03T11:08:04Z
dc.date.issued
2017-08-04
dc.date.issued
2020-07-03T11:08:04Z
dc.identifier
https://hdl.handle.net/2445/167518
dc.description.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.
dc.format
application/pdf
dc.publisher
American Chemical Society
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1021/acs.orglett.71301818
dc.relation
Organic Letters, 2017, vol. 19, num. 15, p. 4050-4053
dc.relation
https://doi.org/10.1021/acs.orglett.71301818
dc.rights
(c) American Chemical Society , 2017
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)
dc.subject
Síntesi orgànica
dc.subject
Compostos heterocíclics
dc.subject
Organic synthesis
dc.subject
Heterocyclic compounds
dc.title
Enantioselective Synthesis of Spiro[indolizidine-1,3 '-oxindoles]
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion
