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. Author manuscript; available in PMC: 2024 Jan 16.
Published in final edited form as: Angew Chem Int Ed Engl. 2022 Dec 8;62(3):e202213055. doi: 10.1002/anie.202213055

Table 2:

Scope of Iron-catalyzed decarboxylative protonation[a]

graphic file with name nihms-1850003-t0009.jpg
[a]

All reactions were conducted on a 0.4 mmol scale.

[b]

2.5 mol% Fe(NO3)3ยท9H2O and 2.5 mol% di(2-picolyl)amine were used.

[c]

The yields were determined by 1H NMR spectroscopy using trimethoxybenzene as an internal standard due to the volatile properties or poor traceability on thin layer chromatography.

[d]

Reaction concentration = 0.05 M; 30 mol% TRIP disulfide were used.

[e]

15 mol% TRIP disulfide were used.