Tetrahedron letters

Mannich reactions of π-excessive heterocycles using bis-(dialkylamino) methanes and alkoxydialkylaminomethanes activated with acetyl chloride or sulphur dioxide

SC Eyley, H Heaney, G Papageorgiou, RF Wilkins

Index: Eyley, Stephen C.; Heaney, Harry; Papageorgiou, George; Wilkins, Robert F. Tetrahedron Letters, 1988 , vol. 29, # 24 p. 2997 - 3000

Full Text: HTML

Citation Number: 23

Abstract

Abstract Π-Excessive heterocycles react rapidly with bis (dialkylamino) methanes (aminals) and alkoxydialkylaminomethanes (aminol ethers) in acetonitrile to afford Mannich bases in good yields when activated by means of an acidic reagent such as acetyl chloride or sulphur dioxide: the principal compound studied was Full-size image (< 1 K)

Related Articles:

The activation of aminals and aminol ethers by sulfur dioxide and their reactions with electron rich aromatic compounds

[Heaney, Harry; Papageorgiou, George; Wilkins, Robert F. Tetrahedron, 1997 , vol. 53, # 39 p. 13361 - 13372]

Mannich Bases from N-Substituted Pyrroles

[Herz; Rogers Journal of the American Chemical Society, 1951 , vol. 73, p. 4921]

More Articles...