1609401-43-5Relevant articles and documents
Nickel-Catalyzed Ortho C–H Methylation of Aromatic Amides with Di-tert-butyl Peroxide as Methylation Reagent
Liu, Da,Yu, Lin,Yu, Yongqi,Xia, Zhen,Song, Zenan,Liao, Lihong,Tan, Ze,Chen, Xiang
supporting information, p. 6930 - 6934 (2019/11/13)
A new efficient protocol for the ortho-methylation of benzamides with DTBP has been developed via Ni(II)-catalyzed C–H activation directed by 8-aminoquinoline. This method is performed under base-free, ligand-free conditions and utilizes cheap and commercially available reagents. Moreover, the by-product acetone derived from DTBP does not affect the purification of the product.
Isoindolone synthesis via palladium-catalysed intramolecular amination of benzylic C-H bonds
Zhang, Ming
, p. 606 - 610 (2013/11/06)
A new method for the construction of isoindolones is presented in this paper. Four 7-methyl-2-(8-quinolinyl)-2,3-dihydro-1Hisoindol-1-ones were synthesised from 2,6-dimethyl -N-(8-quinolinyl)benzamides via intramolecular direct amination of benzylic C-H bonds. This approach provides a convenient method affording structurally new isoindolones for medicinal chemistry research.