前往化源商城

Tetrahedron letters

Acceleration of the DABCO-promoted Baylis–Hillman reaction using a recoverable H-bonding organocatalyst

DJ Maher, SJ Connon

文献索引:Maher, Declan J.; Connon, Stephen J. Tetrahedron Letters, 2004 , vol. 45, # 6 p. 1301 - 1305

全文:HTML全文

被引用次数: 137

摘要

It has been shown that catalytic amounts (20–40mol%) of bis-aryl (thio) ureas greatly accelerate the DABCO-promoted Baylis–Hillman reaction between a range of aromatic aldehydes and methyl acrylate in the absence of solvent. These robust organocatalysts are superior mole per mole promoters of the reaction than either methanol or water and are recoverable in high yield after the reaction by column chromatography.