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TBN as a metal-free reagent initiated sp3 C–H functionalization of glycine esters: Synthesis of quinoline-2-carboxylate esters
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-01-04 , DOI: 10.1016/j.tetlet.2018.01.003 Xiaofei Liu , Yu Shao , Pengfei Li , Honghe Ji , Yu Yuan , Xiaodong Jia
中文翻译:
TBN作为一种无金属试剂,可引发甘氨酸酯的sp 3 C–H官能化:喹啉-2-羧酸酯的合成
更新日期:2018-01-04
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-01-04 , DOI: 10.1016/j.tetlet.2018.01.003 Xiaofei Liu , Yu Shao , Pengfei Li , Honghe Ji , Yu Yuan , Xiaodong Jia
As a metal-free reagent, tert-butylnitrite (TBN) initiated aerobic sp3 C–H bond oxidation of glycine esters was achieved, providing a series of quinoline-2-carboxylates in good yields. The mechanistic investigation revealed that in the presence of molecular oxygen, TBN derived radicals were involved in the C–H bond oxidation and the terminal aromatization.
中文翻译:
TBN作为一种无金属试剂,可引发甘氨酸酯的sp 3 C–H官能化:喹啉-2-羧酸酯的合成
作为一种不含金属的试剂,可实现叔丁基亚硝酸盐(TBN)引发的甘氨酸酯的好氧sp 3 C–H键氧化,从而以良好的收率提供了一系列的喹啉-2-羧酸酯。机理研究表明,在存在分子氧的情况下,TBN衍生的自由基参与了C–H键的氧化和末端芳构化。