128141-03-7Relevant academic research and scientific papers
DDQ-induced dehydrogenation of heterocycles for c-c double bond formation: Synthesis of 2-thiazoles and 2-oxazoles
Li, Xiangnan,Li, Cheng,Yin, Bing,Li, Cong,Liu, Ping,Li, Jianli,Shi, Zhen
, p. 1408 - 1411 (2013/07/26)
Strong as an Ox: 2-Thiazoles and 2-oxazoles are formed by oxidation of 2-thiazolines and 2-oxazolines without requiring substituents at the C4 and C5 positions. DDQ plays an important role as the oxidant in this transformation and metal is unnecessary. This general procedure shows good functional group tolerance and provides a wide variety of 2-thiazoles and 2-oxazoles in moderate to excellent yields.
Synthesis of conjugated tri(hetero)aryl derivatives based on one-pot double Suzuki-miyaura couplings using bifunctional dipotassium phenylene-1,4- bis(trifluoroborate)
Salomone, Antonio,Petrera, Marilena,Coppi, Donato Ivan,Perna, Filippo Maria,Florio, Saverio,Capriati, Vito
, p. 1761 - 1765 (2011/09/12)
An efficient one-pot double Suzuki-Miyaura cross--coupling reaction between bifunctional phenylene-1,4-bis(potassium trifluoroborate) and aryl and heteroaryl bromides is described. The scope and limitations of this methodology that enables the synthesis o
CONVENIENT SYNTHESIS OF VARIOUS TERHETEROCYCLIC COMPOUNDS BY Pd(O)-CATALYZED COUPLING REACTIONS
Gronowitz, Salo,Peters, Dan
, p. 645 - 658 (2007/10/02)
Various terheterocyclic compounds containing thiophene, furan, selenophene, pyridine and thiazole rings have been obtained by the Pd(PPh3)4-catalyzed coupling of dihalo-substituted heterocyclic compounds with heterocyclic boronic acids, using sodium bicar
