dc.contributor.author
Ariza Piquer, Xavier
dc.contributor.author
García Gómez, Jordi
dc.contributor.author
Romea, Pedro
dc.contributor.author
Urpí Tubella, Fèlix
dc.date.issued
2014-04-02T11:09:11Z
dc.date.issued
2014-04-02T11:09:11Z
dc.date.issued
2014-04-02T11:09:11Z
dc.identifier
https://hdl.handle.net/2445/53194
dc.description.abstract
This review deals with metal enolate-mediated stereoselective acetate aldol reactions. It summarizes recent advances on aldol additions of unsubstituted metal enolates from chiral auxiliaries, stoichiometric and catalytic Lewis acids, or acting in substrate- controlled reactions, which provide stereocontrolled aldol transformations that allow the efficient synthesis of structurally complex natural products.
dc.format
application/pdf
dc.publisher
Georg Thieme Verlag
dc.relation
Versió postprint del document publicat a: http://dx.doi.org/10.1055/s-0030-1260040
dc.relation
Synthesis. Journal of Synthetic Organic Chemistry, 2011, vol. 2011, num. 14, p. 2175-2191
dc.relation
http://dx.doi.org/10.1055/s-0030-1260040
dc.rights
(c) Georg Thieme Verlag, 2011
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Química Inorgànica i Orgànica)
dc.subject
Reacció aldòlica
dc.subject
Productes naturals
dc.subject
Aldol reaction
dc.subject
Natural products
dc.title
Stereoselective Acetate Aldol Reactions From Metal Enolates
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion
