Skip to main content
. 2022 Sep 14;87(19):13204–13223. doi: 10.1021/acs.joc.2c01684

Table 3. Exocyclic Olefin Scopea.

graphic file with name jo2c01684_0007.jpg

graphic file with name jo2c01684_0008.jpg

a

Reaction conditions: 0.2 mmol, 1.0 equiv of N-allyltoluenesulfonamide, 1.5 equiv of 1,3-dihalo-5,5′-dimethylhydantoin, 3.0 equiv of olefin, 0.5 mol % (Ir[dF(CF3)ppy]2(dtbpy))PF6, 4 mL total (step 2) of DCM. aDiastereomeric ratios not able to be determined due to inseparability and substantial overlapping of peaks in the 1H NMR spectra of the isolated diastereomers.

b

2 equiv of olefin component used.

c

0.5 mol % 4CzIPN used as photocatalyst instead.