Fig. 2: Substrate scope. | Nature Communications

Fig. 2: Substrate scope.

From: Constructing chiral bicyclo[3.2.1]octanes via palladium-catalyzed asymmetric tandem Heck/carbonylation desymmetrization of cyclopentenes

Fig. 2: Substrate scope.

a Substrate scope of primary alcohols. b Substrate scope of secondary alcohols. c Substrate scope of the benzoylcyclopentenes. Reaction conditions: X = I, 1 (0.1 mmol), 2 (1 mmol), Pd2dba3•CHCl3 (5 mol%), L1 (20 mol%), K2CO3 (0.2 mmol) in 1 mL solvent, 100 °C, 36 h, under CO (1 atm). Yields of isolated products are given. The dr values were determined by 1H NMR analysis. The ee values were determined by HPLC analysis on a chiral stationary phase. aX = Br. b48 h.

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