15 research outputs found
Synthesis of new 1,3-thiazines by a three-compoment reaction of thiobenzamide with aromatic aldehydes and alkenes, under microwaves activation
National audienc
Synthesis of new 1,3-thiazines by a three-compoment reaction of thiobenzamide with aromatic aldehydes and alkenes, under microwaves activation
National audienc
Synthesis of 1,3-thiazines and their applications as precursors of 1,3-aminothiols
AfficheInternational audienc
Synthesis of 1,3-thiazines by a three-component reaction and their transformations into β-lactam-condensed 1,3-thiazine and 1,4-thiazepine derivatives
International audienceVariously substituted 1,3-thiazines have been prepared by a three-component reaction involving a thioamide, an aldehyde, and an alkene. Two diastereomeric thiazines were transformed by stereoselective Staudinger reaction into the corresponding chloro-β-lactam-condensed-1,3-thiazines, and one of them was rearranged in basic media to afford a highly substituted 1,4-thiazepine. Several of the obtained compounds (six 1,3-thiazines and one β-lactam-condensed-1,3-thiazine) were analyzed by X-ray crystallography, which enabled to assign their spatial arrangement and stereochemistry
Asymmetric Three-Component Domino Reaction: An Original Access to Chiral Nonracemic 1,3-Thiazin-2-ones
International audienc