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. Author manuscript; available in PMC: 2021 Feb 10.
Published in final edited form as: Angew Chem Int Ed Engl. 2020 Jan 8;59(7):2674–2678. doi: 10.1002/anie.201913730

Table 2:

The scope of the oxygen nucleophile in the Pd-based cyclization.[a,b]

graphic file with name nihms-1561410-t0005.jpg
[a]

Reaction conditions unless otherwise noted: 17 (0.1 mmol), Pd-(OAc)2 (0.01 mmol), t-BuMephos (0.015 mol), acetate source (0.3 mmol), toluene (1 mL), 90°C, 5 h.

[b]

Yields shown are of isolated products.

[c]

Reaction temperature was 130°C.