Tetrahedron

Exploring the versatility of the Johnson–Claisen rearrangement: access to functionally versatile δ-ethoxycarbonyl-α, β-unsaturated nitriles

KL Cosgrove, RP McGeary

Index: Cosgrove, Kelly L.; McGeary, Ross P. Tetrahedron, 2010 , vol. 66, # 16 p. 3050 - 3057

Full Text: HTML

Citation Number: 6

Abstract

A practical entry into δ-ethoxycarbonyl-α, β-unsaturated nitriles is described. α, β- Unsaturated aldehydes were converted to cyanohydrins, by employing either KCN in aqueous acid, or by using TMSCN with catalytic K2CO3, followed by acid hydrolysis of the TMS ether. These cyanohydrins underwent a Claisen rearrangement employing a modified Johnson–Claisen protocol to yield unsaturated nitriles in good yields and with moderate E ...

Related Articles:

Vanadium-catalyzed asymmetric oxidation of α-hydroxy esters using molecular oxygen as stoichiometric oxidant

[Radosevich, Alexander T.; Musich, Christine; Toste, F. Dean Journal of the American Chemical Society, 2005 , vol. 127, # 4 p. 1090 - 1091]

Naturally occurring cyanohydrins, analogues and derivatives as potential insecticides

[Peterson, Chris J.; Tsao, Rong; Coats, Joel R. Pest Management Science, 2000 , vol. 56, # 7 p. 615 - 617]

More Articles...