83783-36-2Relevant academic research and scientific papers
Selective C-H acylation of indoles with α-oxocarboxylic acids at the C4 position by palladium catalysis
Zhang, Jitan,Wu, Manyi,Fan, Jian,Xu, Qiaoqiao,Xie, Meihua
, p. 8102 - 8105 (2019)
The first Pd-catalyzed direct C-H acylation of indoles at the C4 position with α-oxocarboxylic acids using a ketone directing group is described. This reaction exhibits high regioselectivity with the tolerance of a wide scope of functional groups to afford diverse acylated indoles in moderate-to-good yields. The control experiments evidence the generation of acyl radicals via K2S2O8 promoted decarboxylation of α-oxocarboxylic acids and the involvement of a PdII/PdIV catalytic cycle. Importantly, the synthetically useful selectivity observed might be applied to prepare indole derivatives with anti-tumor activity as tubulin inhibitors.
Aromatic Amidines: Comparison of Their Ability to Block Respiratory Syncytial Virus Induced Cell Fusion and to Inhibit Plasmin, Urokinase, Thrombin, and Trypsin
Tidwell, R. R.,Geratz, J. D.,Dubovi, E. J.
, p. 294 - 298 (2007/10/02)
Two series of amidine derivatives consisting of a total of 24 compounds were examined for a correlation between their blocking effect on respiratory syncytial virus induced cell fusion and their inhibitory activity against selected trypsin-like protease.A
