Regioselective syntheses of 1-aryl-substituted-5H-[1,3]thiazolo[3,2-a]quinazoline-5-ones during Sonogashira coupling was written by Bakherad, Mohammad;Keivanloo, Ali;Kalantar, Zahra;Keley, Vahid. And the article was included in Phosphorus, Sulfur and Silicon and the Related Elements in 2011.Category: iodides-buliding-blocks The following contents are mentioned in the article:
Reaction of 2-mercaptopropargyl quinazolin-4-one (I) with various aryl iodides catalyzed by Pd-Cu leads to the regioselective formation of 1-aryl substituted-5H-[1,3]thiazolo-[3,2-a]quinazoline-5-ones, e.g., II. This study involved multiple reactions and reactants, such as 2-Chloro-4-iodobenzonitrile (cas: 371764-70-4Category: iodides-buliding-blocks).
2-Chloro-4-iodobenzonitrile (cas: 371764-70-4) belongs to iodide derivatives. In addition to tryptophan, indigo, and indoleacetic acid, numerous compounds obtainable from plant or animal sources contain the indole molecular structure. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Category: iodides-buliding-blocks
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com