Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164139
Title: A practical synthetic route to enantiopure 6-substituted cis-decahydroquinolines
Author: Amat Tusón, Mercedes
Navío, Laura
Llor Brunés, Núria
Molins, Elies
Bosch Cartes, Joan
Keywords: Síntesi orgànica
Lactames
Enantiòmers
Compostos heterocíclics
Organic synthesis
Lactams
Enantiomers
Heterocyclic compounds
Issue Date: 6-Jan-2012
Publisher: American Chemical Society
Abstract: Starting from 4-substituted cyclohexanones, a practical synthetic route to enantiopure 6-substituted cis-decahydroquinolines has been developed, the key steps being a stereoselective cyclocondensation of an unsaturated δ-keto ester derivative with (R)-phenylglycinol and the stereoselective hydrogenation of the resulting tricyclic oxazoloquinolone lactams.
Note: Versió postprint del document publicat a: https://doi.org/10.1021/ol2030058
It is part of: Organic Letters, 2012, vol. 14, num. 1, p. 210-213
URI: http://hdl.handle.net/2445/164139
Related resource: https://doi.org/10.1021/ol2030058
ISSN: 1523-7060
Appears in Collections:Articles publicats en revistes (Institut de Biomedicina (IBUB))
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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