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. Author manuscript; available in PMC: 2023 Aug 1.
Published in final edited form as: Angew Chem Int Ed Engl. 2022 Jun 10;61(31):e202200334. doi: 10.1002/anie.202200334

Table 2.

Reactions with trimethylsilyldiazomethane.

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Catalyst (1 mol%), entries 1 and 3: CH2Cl2 (6.5 mL), substrate (2.5 mmol, 5.0 equiv), add Me3SiCHN2 (0.5 mmol, 1.0 equiv, in hexanes + 6.5 mL CH2Cl2) in 6 hours at RT. Rest of entries: substrate used as solvent (10 mL, 128–246 equiv). Yields are isolated yields. [a] Isolated as a mixture of isomers. [b] Yield determined by 1H NMR spectroscopy with an internal standard.