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. Author manuscript; available in PMC: 2020 Nov 4.
Published in final edited form as: ChemSusChem. 2019 Jun 5;12(13):3003–3007. doi: 10.1002/cssc.201900727

Figure 5.

Figure 5.

Substrate scope. NMR % yield relative to 1,3,5-trimethoxybenzene (isolated % yield in parentheses). Average of two reactions. [a] Isolated yield on 1 g scale: 80% [b] Yields obtained using t-butylbenzoquinone due to co-elution with 2,6-dimethylbenzoquinone during column chromatography purification.