dc.contributor.author
Griera Farres, Rosa
dc.contributor.author
Pinto, Alexandre
dc.contributor.author
Fabregat, Robert
dc.contributor.author
Cots, Èric
dc.contributor.author
Bosch Cartes, Joan
dc.contributor.author
Amat Tusón, Mercedes
dc.date.issued
2019-01-25T10:06:09Z
dc.date.issued
2019-12-31T06:10:14Z
dc.date.issued
2019-01-25T10:06:09Z
dc.identifier
https://hdl.handle.net/2445/127602
dc.description.abstract
In the search for synthetic routes for the preparation of cis- and trans- decahydroquinolin-2- ones, a procedure for the generation of enantiopure trans-hydrochromene lactones, by treatment of (R)- phenylglycinol-derived oxazoloquinolone lactams with Na/liq. NH3 followed by acidification, has been developed.
dc.format
application/pdf
dc.format
application/pdf
dc.publisher
Bentham Science Publishers
dc.relation
Versió postprint del document publicat a: https://doi.org/10.2174/1570178615666171213143657
dc.relation
Letters In Organic Chemistry, 2018, vol. 15, num. 5, p. 335-339
dc.relation
https://doi.org/10.2174/1570178615666171213143657
dc.rights
(c) Bentham Science Publishers, 2018
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
Removal of the chiral inductor from phenylglycinol-derived tricyclic lactams. Unexpected generation of chiral trans-hydrochromene lactones
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion
