95891-75-1Relevant articles and documents
Diethylaluminum ethoxide mediated crossed aldol reaction of enol esters with carbonyl compounds
Mukaiyama, Teruaki,Shibata, Jun,Shimamura, Tadashi,Shiina, Isamu
, p. 951 - 952 (2007/10/03)
Crossed aldol reaction of enol esters, stable carbon nucleophiles, with carbonyl compounds is effectively performed by the promotion of diethylaluminum ethoxide under mild conditions. This reaction is applicable not only to simple enol esters but also to
New 4,5 (3H)dihydro-4-acetyl-2-furanones derivatives: Chemical and pharmacological study
Couquelet,Taoufik,Couquelet,et al.
, p. 301 - 305 (2007/10/02)
5-substituted 4,5 (3H)-dihydro 4-acetyl 2-furanones were synthetized by reaction of aromatic heteroaromatic or cyclanic aldehydes with α-angelicalactone in presence of boron trifluoride. We showed from NMR spectroscopic data that the reaction course was s