1087752-99-5Relevant academic research and scientific papers
Asymmetric aldol reaction with diisopinocampheyl enolborinates of propionates
Ramachandran, P. Veeraraghavan,Pratihar, Debarshi
supporting information; experimental part, p. 1467 - 1470 (2009/08/07)
A convenient and general, reagent-controlled, diastereo-and enantioselective aldol reaction of diisopinocampheylboron enolates of esters, followed by reduction, has been developed as an alternative to crotylboration-ozonolysis. This protocol was then expl
STEREOSELECTIVE REDUCTION OF β-KETO ESTERS WITH ZINC BOROHYDRIDE. STEROSELECTIVE SYNTHESIS OF ERYTHRO-3-HYDROXY-2-ALKYLPROPIONATES
Nakata, Tadashi,Oishi, Takeshi
, p. 1641 - 1644 (2007/10/02)
Erythro-3-hydroxy-2-alkylpropionates were prepared in high stereoselectivity and in high isolated yield by zinc borohydride reduction of the corresponding β-keto esters.
