- -

Enantioselective synthesis of 2-substituted-1,4-diketones from (S)-mandelic acid enolate and alpha, beta-enones

RiuNet: Institutional repository of the Polithecnic University of Valencia

Share/Send to

Cited by

Statistics

Enantioselective synthesis of 2-substituted-1,4-diketones from (S)-mandelic acid enolate and alpha, beta-enones

Show full item record

Blay, G.; Fernandez, I.; Monje, B.; Muñoz Roca, MDC.; Pedro, JR.; Vila, C. (2006). Enantioselective synthesis of 2-substituted-1,4-diketones from (S)-mandelic acid enolate and alpha, beta-enones. Tetrahedron. 62(39):9174-9182. https://doi.org/10.1016/j.tet.2006.07.036

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/151882

Files in this item

Item Metadata

Title: Enantioselective synthesis of 2-substituted-1,4-diketones from (S)-mandelic acid enolate and alpha, beta-enones
Author: Blay, Gonzalo Fernandez, Isabel Monje, Belen Muñoz Roca, María Del Carmen Pedro, Jose R. Vila, Carlos
UPV Unit: Universitat Politècnica de València. Departamento de Física Aplicada - Departament de Física Aplicada
Issued date:
Abstract:
[EN] An approach for the synthesis of chiral non-racemic 2-substituted-1,4-diketones from (S)-mandelic acid and ¿,ß-enones has been developed. The reaction of lithium enolate of the 1,3-dioxolan-4-one derived from optically ...[+]
Copyrigths: Cerrado
Source:
Tetrahedron. (issn: 0040-4020 )
DOI: 10.1016/j.tet.2006.07.036
Publisher:
Elsevier
Publisher version: https://doi.org/10.1016/j.tet.2006.07.036
Project ID:
MCYT/BQU2001-3017
GV/GV05/10
GV/03/168
Thanks:
Financial support from the Spanish Government MEC (BQU2001-3017) and from Generalitat Valenciana (Grupos 03/168 and GV05/10) is acknowledged. B.M. thanks the MEC for a grant (FPI program).
Type: Artículo

This item appears in the following Collection(s)

Show full item record