Assembly of Indoline-2-carboxylate-Embodied Dipeptides via Pd-Catalyzed C(sp<sup>2</sup>)–H Bond Direct Functionalization Yu-Peng He Chao Zhang Mengyang Fan Zhijie Wu Dawei Ma 10.1021/ol503514t.s001 https://acs.figshare.com/articles/journal_contribution/Assembly_of_Indoline_2_carboxylate_Embodied_Dipeptides_via_Pd_Catalyzed_C_sp_sup_2_sup_H_Bond_Direct_Functionalization/2208736 Intramolecular dehydrogenative cyclization of 2-methoxyiminoacyl-protected phenylalanine derivatives proceeded at 110 °C under catalysis of Pd­(OAc)<sub>2</sub> in the presence of 1-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate to afford substituted indoline-2-carboxylates that were converted into indoline-2-carboxylate-embodied dipeptides via Raney Ni-catalyzed hydrogenation. 2015-02-06 00:00:00 Indoline presence phenylalanine Pd hydrogenation indoline assembly catalysi Raney derivative Bond tetrafluoroborate dipeptide Dipeptide FunctionalizationIntramolecular dehydrogenative cyclization fluoro