Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164192
Title: Cyclocondensation reactions of 2-acyl-3-indoleacetic acid derivatives with phenylglycinol. Enantioselective synthesis of 1-substituted tetrahydro-b-carboline alkaloids
Author: Amat Tusón, Mercedes
Subrizi, Fabiana
Elias, Viviane
Llor Brunés, Núria
Molins, Elies
Bosch Cartes, Joan
Keywords: Síntesi asimètrica
Alcaloides
Lactames
Asymmetric synthesis
Alkaloids
Lactams
Issue Date: Mar-2012
Publisher: Wiley-VCH
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.
Note: Versió postprint del document publicat a: https://doi.org/10.1002/ejoc.201101718
It is part of: European Journal of Organic Chemistry, 2012, vol. 2012, num. 9, p. 1835-1842
URI: http://hdl.handle.net/2445/164192
Related resource: https://doi.org/10.1002/ejoc.201101718
ISSN: 1434-193X
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
Articles publicats en revistes (Institut de Biomedicina (IBUB))

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