Pd-Catalyzed Enantioselective C–H Iodination: Asymmetric Synthesis of Chiral Diarylmethylamines Ling Chu Xiao-Chen Wang Curtis E. Moore Arnold L. Rheingold Jin-Quan Yu 10.1021/ja408864c.s001 https://acs.figshare.com/articles/journal_contribution/Pd_Catalyzed_Enantioselective_C_H_Iodination_Asymmetric_Synthesis_of_Chiral_Diarylmethylamines/2359600 An enantioselective C–H iodination reaction using a mono-<i>N</i>-benzoyl-protected amino acid has been developed for the synthesis of chiral diarylmethylamines. The reaction uses iodine as the sole oxidant and proceeds at ambient temperature and under air. 2013-11-06 00:00:00 Enantioselective iodine ambient temperature acid enantioselective proceed Iodination synthesis Asymmetric Synthesis Chiral oxidant chiral diarylmethylamines iodination DiarylmethylaminesAn