Synthesis of 2-acetyl-1-pyrroline, the principal rice flavor component
NG De Kimpe, CV Stevens…
Index: Kimpe, Norbert G. De; Stevens, Christian V.; Keppens, Marian A. Journal of Agricultural and Food Chemistry, 1993 , vol. 41, # 9 p. 1458 - 1461
Full Text: HTML
Citation Number: 47
Abstract
A new straightforward synthesis of 2-acetyl-l-pyrroline, the principal rice flavor component with a cracker-like flavor, is reported. The reaction sequence involves the conversion of pyrrolidine into tripyrroline, subsequent hydrocyanation of the latter into 2-cyanopyrrolidine, oxidation into 2-cyano-1-pyrroline, and Grignard addition of methylmagnesium iodide, affording an overall yield of 16-19 7% from pyrrolidine. In similar way, 2-propionyl-l- ...
Related Articles:
Orientation Sensitive Peptide Induced Plasmonic Circular Dichroism in Silver Nanocubes
[Reuter, Cedric; Huy, Peter; Neudoerfl, Joerg-Martin; Kuehne, Ronald; Schmalz, Hans-Guenther Chemistry - A European Journal, 2011 , vol. 17, # 43 p. 12037 - 12044]
Orientation Sensitive Peptide Induced Plasmonic Circular Dichroism in Silver Nanocubes
[Reuter, Cedric; Huy, Peter; Neudoerfl, Joerg-Martin; Kuehne, Ronald; Schmalz, Hans-Guenther Chemistry - A European Journal, 2011 , vol. 17, # 43 p. 12037 - 12044]