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