The Benary reaction is an organic reaction. In 1931 Erich Bénary discovered that β-(N,N-dialkylamino)-vinyl ketones reacted with Grignard reagents in a...

The Feist–Benary synthesis is an organic reaction between α-halo ketones and β-dicarbonyl compounds to produce substituted furan compounds. This condensation...

Bellus–Claisen rearrangement Belousov–Zhabotinsky reaction Benary reaction Benedict's reagent Benkeser reaction Benzidine rearrangement Benzilic acid rearrangement...

this reaction would induce self-condensation of the aldehyde or ketone. The Hantzsch pyridine synthesis, the Gewald reaction and the Feist–Benary furan...

condensation Diels–Alder reaction Feist–Benary synthesis Fiesselmann thiophene synthesis Fischer indole synthesis Gewald reaction Hantzsch pyridine synthesis...

solids, especially pine wood. The Feist–Benary synthesis is a classic way to synthesize furans. The reaction involves alkylation of 1,3-diketones with...

fused furans. Hantzsch pyrrole synthesis Knorr pyrrole synthesis Feist–Benary synthesis Volhard–Erdmann cyclization Hantzsch pyridine synthesis Paal,...

in chemical manufacturing. It is also used in the Feist-Benary synthesis of furans. Reaction of phenoxide with chloroacetone gives phenoxyacetone, which...

versatile intermediate. 2,3-Dihydrofurans are intermediates in the Feist–Benary synthesis of furans from α-halogen ketones and β-dicarbonyl compounds. The...

pp. 569–570. Miller, p. 25. Lankford, p. 44. Diamond, Beverly; Barbara Benary. "Indonesian Music". The Garland Encyclopedia of World Music. pp. 1011–1023...