Sur les organometalliques issus de thioamides: I. Reactivite avec les aldehydes et cetones; stereochimie de la condensation avec la t-butyl-4 cyclohexanone et le …

…, N Goasdoue, M Gaudemar, M Mladenova

Index: Goasdoue, Claude; Goasdoue, Nicole; Gaudemar, Marcel; Mladenova, Margarita Journal of Organometallic Chemistry, 1981 , vol. 208, # 3 p. 279 - 292

Full Text: HTML

Citation Number: 29

Abstract

Abstract Organometallic compounds derived from thioamides RCH 2 CSN (R 3) 2 condense normally with aldehydes and saturated ketones. Condensation with 4-t-butyl-cyclohexanone leads predominantly to equatorial attack by the organometallic compound. These results suggest that the organometallic structure as RCH C (SM) N (R 3) 2.

Related Articles:

Carbon versus sulfur addition of nucleophiles to sulfines: the case of amines

[Cerreta, Francesca; Leriverend, Catherine; Metzner, Patrick Tetrahedron Letters, 1993 , vol. 34, # 42 p. 6741 - 6742]

1, 4-Addition reaction of organolithium and-magnesium compounds to. alpha.,. beta.-unsaturated thioamides

[Tamaru,Y. et al. Journal of the American Chemical Society, 1978 , vol. 100, p. 5221 - 5223]

More Articles...