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. Author manuscript; available in PMC: 2020 Nov 13.
Published in final edited form as: J Am Chem Soc. 2019 Nov 1;141(45):18160–18169. doi: 10.1021/jacs.9b08894

Table 3.

Ligand Effect on Co(II)-Catalyzed Asymmetric 1,5-C–H Amination of Alkylsulfonyl Azides 3aa

graphic file with name nihms-1057584-t0005.jpg
entry catalyst solvent yield (%) ee (%)
1 [Co(P4)] benzene 10 90
2 [Co(P1)] benzene 97 48
3 [Co(P5)] benzene 99 69
4 [Co(P6)] benzene 92 94
5 [Co(P6)] chlorobenzene 95 91
6 [Co(P6)] chloroform 95 84
graphic file with name nihms-1057584-t0006.jpg
a

Reactions were carried out at 40 °C for 18 h on 0.25 mmol scale under N2; [3a] = 0.10 M; isolated yields enantiomeric excess determined by chiral HPLC.