dc.contributor.author
Amat Tusón, Mercedes
dc.contributor.author
Subrizi, Fabiana
dc.contributor.author
Elias, Viviane
dc.contributor.author
Llor Brunés, Núria
dc.contributor.author
Molins, Elies
dc.contributor.author
Bosch Cartes, Joan
dc.date.issued
2020-06-04T07:42:42Z
dc.date.issued
2020-06-04T07:42:42Z
dc.date.issued
2020-06-04T07:42:42Z
dc.identifier
https://hdl.handle.net/2445/164192
dc.description.abstract
Cyclocondensation reactions between a variety of 2‐acyl‐3‐indoleacetic acid derivatives and (R )‐phenylglycinol were studied. Successful results were obtained from N ‐alkyl keto acid derivatives. The resulting tetracyclic lactams provide straightforward access to enantiopure 1‐substituted tetrahydro‐β‐carboline alkaloids.
dc.format
application/pdf
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1002/ejoc.201101718
dc.relation
European Journal of Organic Chemistry, 2012, vol. 2012, num. 9, p. 1835-1842
dc.relation
https://doi.org/10.1002/ejoc.201101718
dc.rights
(c) Wiley-VCH, 2012
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject
Síntesi asimètrica
dc.subject
Asymmetric synthesis
dc.title
Cyclocondensation reactions of 2-acyl-3-indoleacetic acid derivatives with phenylglycinol. Enantioselective synthesis of 1-substituted tetrahydro-b-carboline alkaloids
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion
