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. Author manuscript; available in PMC: 2019 Apr 11.
Published in final edited form as: J Am Chem Soc. 2018 Mar 29;140(14):4797–4802. doi: 10.1021/jacs.8b02143

Figure 4.

Figure 4

Extension of the fluoroamination reaction protocol. a, Formation of 1,3-difluoro-2-amines bearing three contiguous ste-reocenters from enantioenriched allylic sulfonamides. b, Fluoroam-ination of bis-homoallylic sulfonamide 7 results in formation of the corresponding anti-β-fluoropyrrolidine. Isolated yields are indicated below all products; the yield in parentheses corresponds to re-crystallized product. Full experimental details are provided in the Supplementary Information.