Skip to main content
. Author manuscript; available in PMC: 2018 Apr 12.
Published in final edited form as: J Am Chem Soc. 2018 Feb 21;140(9):3394–3402. doi: 10.1021/jacs.7b13616

Table 3.

Scope of mesolytic bond cleavage induced nucleophilic substitution.a

graphic file with name nihms956192f7.jpg
a

Reactions run on a 0.25 mmol scale. Reported yields are for isolated and purified materials. The optical purity of all products was confirmed by HPLC analysis.

b

Unprotected pyrroloindoline 2 as the substrate.

c

Conducted with 6 equiv. of sulfamide.