Synlett

An Improved Procedure for the Photoacylation of 1, 4-Naphthoquinone with Aliphatic Aldehydes

F Friedrichs, B Murphy, D Nayrat, T Ahner, M Funke…

Index: Friedrichs, Ferdinand; Murphy, Brian; Nayrat, Delphine; Ahner, Torsten; Funke, Mario; Ryan, Michael; Lex, Johann; Mattay, Jochen; Oelgemoeller, Michael Synlett, 2008 , # 20 p. 3137 - 3140

Full Text: HTML

Citation Number: 3

Abstract

Abstract Irradiation of 1, 4-naphthoquinone at 300±25 nm in benzene and in the presence of aliphatic aldehydes readily yields acylated hydroquinones in good to high yields. The developed protocol represents a significant improvement over the original procedure using medium-pressure mercury lamps. Subsequent oxidation gives the corresponding acylated quinones.

Related Articles:

The “Photo??Friedel− Crafts Acylation” of 1, 4??Naphthoquinones

[Oelgemoeller, Michael; Schiel, Christian; Froehlich, Roland; Mattay, Jochen European Journal of Organic Chemistry, 2002 , # 15 p. 2465 - 2474]

Fast, easy, and efficient method for the purification of phenolic isomers using a selective solid-phase scavenging process

[Rieck, John A.; Grunwell, John R. Journal of Organic Chemistry, 1980 , vol. 45, # 17 p. 3512 - 3513]

Fast, easy, and efficient method for the purification of phenolic isomers using a selective solid-phase scavenging process

[Rieck, John A.; Grunwell, John R. Journal of Organic Chemistry, 1980 , vol. 45, # 17 p. 3512 - 3513]

More Articles...