133415-16-4Relevant articles and documents
Aryl-aryl coupling via palladium-catalyzed C-P/C-H bond cleavage
Li, Ziyuan,Zhou, Haipin,Xu, Jinyi,Wu, Xiaoming,Yao, Hequan
supporting information, p. 3281 - 3286 (2013/04/24)
The first example of aryl-aryl coupling through palladium-catalyzed C-P/C-H bond cleavage with good functional group tolerance is disclosed. This work demonstrates the phosphines could be used as coupling partners in palladium-catalyzed aryl-aryl coupling
Mechanism selection for regiocontrol in base-assisted, palladium-catalysed direct C-H coupling with halides: First approach for oxazole- and thiazole-4-carboxylates
Théveau, Laure,Verrier, Cécile,Lassalas, Pierrik,Martin, Thibaut,Dupas, Georges,Querolle, Olivier,Van Hijfte, Luc,Marsais, Francis,Hoarau, Christophe
supporting information; scheme or table, p. 14450 - 14463 (2012/01/15)
Both base-assisted non-concerted metallation-deprotonation (nCMD) and concerted metallation-deprotonation (CMD) have been identified as two potent operating mechanisms in palladium-catalysed direct C-H coupling of oxazole and thiazole-4-carboxylate esters
SYNTHESIS OF NOVEL THIAZOLES BEARING HYDRAZINE, THIOSEMICARBAZIDE, THIAZOLE, AND THIAZOLIDINONE MOIETIES
Mamedov, V. A.,Nuretdinov, I. A.,Sibgatullina, F. G.
, p. 2470 - 2474 (2007/10/02)
Thiazolecarboxylate esters (I) and (II) react with hydrazine hydrate to give the acid hydrazides (III) and (IV), which then react with KSCN and PhNCS to give high yields of the thiosemicarbazides (V)-(VIII).Cyclocondensation of the thiosemicarbazide (V) w
