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. Author manuscript; available in PMC: 2019 Jan 26.
Published in final edited form as: Angew Chem Int Ed Engl. 2018 Jan 4;57(5):1390–1393. doi: 10.1002/anie.201712015

Table 3.

Enantioselective iridium catalyzed internal redox allylation of phthalaldehyde 1a using substituted allylic acetates 2b–2j to form phthalides 3g–3o.a

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a

Yields are of material isolated by silica gel chromatography. Enantioselectivities were determined by chiral stationary phase HPLC analysis. See Supporting Information for further experimental details.

b

2d (300 mol%).

c

THF (1 M).