An expedient stereoselective access to (Z)-2-fluoroalkenoates
1993; Elsevier BV; Volume: 34; Issue: 43 Linguagem: Inglês
10.1016/s0040-4039(00)91826-4
ISSN1873-3581
AutoresDenis Clemenceau, Jack Cousseau,
Tópico(s)Inorganic Fluorides and Related Compounds
ResumoThe reaction between an aldehyde R-CHO and diethyl 2-oxo-3-fluorobutan-1,4-dioate as its sodium salt EtO2C-CO-CF-CO2Et−, Na+ mainly leads in THF to (Z)-2-fluoroalkenoates R-CHCF-CO2Et (Z/E& > -80/20), the Z-stereoselectivity depending on the bulk of the R group.
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