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. 2024 Nov 20. Online ahead of print. doi: 10.1039/d4sc06458e

Scheme 2. Substrate scope of propargylic esters and alkenes. Reaction conditions: 1 (0.2 mmol), 2 (0.4 mmol), Rh2(OPiv)4 (1 mol%), 1,2-dichloroethane (2 mL), 80 °C, 48 h. a NMR yield with 4-nitrotoluene as the internal standard. Note: 3es was unstable during purification with silica gel.

Scheme 2