58861-66-8Relevant academic research and scientific papers
Pd(ii)-catalyzed direct C5-arylation of azole-4-carboxylates through double C-H bond cleavage
Li, Ziyuan,Ma, Ling,Xu, Jinyi,Kong, Lingyi,Wu, Xiaoming,Yao, Hequan
supporting information; scheme or table, p. 3763 - 3765 (2012/06/15)
The first palladium-catalyzed direct C5-arylation of azole-4-carboxylates with simple unactivated arenes through double C-H bond cleavage is realized. This protocol provided a straightforward access to diverse 5-arylsubstituted azole-4-carboxylic derivatives with good functional group tolerance. The Royal Society of Chemistry 2012.
FORMATION DE 2H-1,4-THIAZINES, 2-BENZYLTHIAZOLES ET 2-BENZOYLTHIAZOLES PAR ACTION DE LA SILICE SUR LES 4-AMINO-3,4-DIHYDRO-2H-1,4-THIAZINES
Besbes, R.,Reliquet, A.,Reliquet, F.,Meslin, J. C.
, p. 123 - 130 (2007/10/02)
In the presence of silica, 4-dimethylamino-3,4-dihydro-2H-1,4-thiazines 1 afford 2H-1,4-thiazines 2 with good yields, 2-benzyl-4-methoxycarbonylthiazoles 3 or 2-aroyl-4-methoxycarbonylthiazoles 4 depending on substituents bound to the thiazinic cycle and experimental conditions.As for 2H-1,4-thiazines 2, they give rise to bisthiazines by a duplication reaction. Key words: 2-(Dialkylhydrazono)thioacetophenones; 3,4-dihydro-2H-1,4-thiazines; 2H-1,4-thiazines; 2-benzyl-4-methoxycarbonylthiazoles; 2-aroyl-4-methoxycarbonylthiazoles.
