Threo selective cross aldol condensation with thioamide enolates generated by a michael addition of organometallics to unsaturated thioamides

Authors :: Yoshinao Tamaru
Zen-ichi Yoshida
T. Hioki
Source :: Tetrahedron Letters. 25:5793-5796
Publication Year :: 1984
Publisher :: Elsevier BV, 1984.
Abstract: Crotonothioamide, sorbothioamide, and cinnamothioamide undergo a threo selective aldol condensation via their enolates generated by a Michael addition of organometallics.

Subjects :: chemistry.chemical_classification
Benzaldehyde
chemistry.chemical_compound
Chemistry
Organic Chemistry
Drug Discovery
Michael reaction
Organic chemistry
Aldol condensation
Stereoselectivity
Aliphatic compound
Biochemistry
Thioamide

Full Text Access

Tools