Department of Chemistry , Marquette University , Milwaukee , Wisconsin 53201-1881 United States.
Org Lett. 2019 May 3;21(9):3337-3341. doi: 10.1021/acs.orglett.9b01082. Epub 2019 Apr 19.
The in situ formed ruthenium catalytic system ([Ru]/L) was found to be highly selective for the dehydrogenative coupling reaction of 2-aminophenyl ketones with amines to form quinazoline products. The deaminative coupling reaction of 2-aminobenzamides with amines led to the efficient formation of quinazolinone products. The catalytic coupling method provides an efficient synthesis of quinazoline and quinazolinone derivatives without using any reactive reagents or forming any toxic byproducts.
原位形成的钌催化体系([Ru]/L)被发现对 2-氨基苯甲酮与胺脱氢偶联反应具有高度选择性,生成喹唑啉产物。2-氨基苯甲酰胺与胺的脱氨偶联反应导致喹唑啉酮产物的高效形成。该催化偶联方法提供了一种有效合成喹唑啉和喹唑啉酮衍生物的方法,无需使用任何反应试剂或形成任何有毒副产物。
Mol Divers. 2016-8
Chem Commun (Camb). 2009-11-26
Chem Commun (Camb). 2010-4-21
Acta Crystallogr E Crystallogr Commun. 2025-1-17
Pharmaceuticals (Basel). 2024-2-7
Front Chem. 2023-3-16
J Am Chem Soc. 2022-10-26