Lewis acid catalysis of photochemical reactions. 5. Selective isomerization of conjugated butenoic and dienoic esters

…, DK Howard, SV Barancyk, JD Oxman

Index: Lewis, Frederick D.; Howard, Daniel K.; Barancyk, Steven V.; Oxman, Joe D. Journal of the American Chemical Society, 1986 , vol. 108, # 11 p. 3016 - 3023

Full Text: HTML

Citation Number: 31

Abstract

Abstract: The effects of Lewis and Brornsted acids upon the photoisomerization reactions of several conjugated butenoic and dienoic esters have been investigated. Lewis acids inhibit the photochemical deconjugation of a& to 0, y-unsaturated butenoic esters and shift the photoequilibrium between E and Z isomers toward the Z isomer. As such, irradiation of E a, P-unsaturated esters in the presence of EtAlCI, provides a convenient method for the ...

Related Articles:

Conversion of. alpha.,. beta.-unsaturated esters to their. beta.,. gamma.-unsaturated isomers by photochemical deconjugation

[Duhaime, Randy M.; Lombardo, Domenic A.; Skinner, Ian A.; Weedon, Alan C. Journal of Organic Chemistry, 1985 , vol. 50, # 6 p. 873 - 879]

Action d'organozinciques α-ethyleniques sur le chloroformiate d'ethyle: preparation d'esters β-ethyleniques

[Miginiac,P.; Zamlouty,G. Journal of Organometallic Chemistry, 1975 , vol. 96, p. 163 - 168]

More Articles...