RT Journal Article
T1 Mild and High-Yielding Synthesis of β-Keto Esters and β-Ketoamides
A1 Sridharan, Vellaisamy
A1 Menéndez Ramos, José Carlos
A1 Ruiz Serrano, Miriam
AB In the presence of sodium acetate, the reaction between 2,2,6-trimethyl-4H-1,3-dioxin-4-one and secondary or tertiary alcohols (including chiral ones) or primary or secondary amines could be carried out in refluxing tetrahydrofuran, under much milder conditions than those described in the literature. In these new conditions, side products normally observed using the traditional protocol were avoided, and b-keto esters and b-ketoamides were normally obtained in quantitative yields
PB Thieme Gruppe
SN 0039-7881
YR 2009
FD 2009
LK https://hdl.handle.net/20.500.14352/129002
UL https://hdl.handle.net/20.500.14352/129002
LA eng
NO Sridharan V, Ruiz M, Menéndez J. Mild and High-Yielding Synthesis of β-Keto Esters and β-Ketoamides. Synthesis 2010;2010:1053–7. https://doi.org/10.1055/s-0029-1217135.
NO Ministerio de Ciencia, Innovación y Universidades (España)
NO Universidad Complutense de Madrid
NO Comunidad de Madrid
DS Docta Complutense
RD 31 dic 2025