1, 4 Addition of acyl groups to conjugated enones

EJ Corey, LS Hegedus

Index: Corey,E.J.; Hegedus,L.S. Journal of the American Chemical Society, 1969 , vol. 91, p. 4926 - 4928

Full Text: HTML

Citation Number: 88

Abstract

'L dicarbonyl structures by intermolecular coupling is not possible using classical synthetic reactions, and consequently indirect approaches have been required, eg, a sequence employing the conjugate addition of nitrostabilized carbanions to enones. The reaction of conjugated enones with 2-lithio-1, 3-dithianes, which are synthetically equivalent to C- nucleophilic carbonyl group^,^ leads only to 1, 2 addition to the enone~ ystem,~ and other ...

Related Articles:

Hydroacylation of Michael acceptors through sequential insertion reactions of organotetracarbonylferrates

[Cooke,M.P.; Parlman,R.M. Journal of the American Chemical Society, 1977 , vol. 99, p. 5222 - 5224]

More Articles...