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. 2015 Jul 22;137(30):9559–9562. doi: 10.1021/jacs.5b06068

Table 1. Optimization Studies for Palladium(II)-Catalyzed Oxidative Carbocyclizationsa.

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a

Reaction conditions: 1a (0.1 mmol), Pd-cat (5–10 mol %), additive (0.2 equiv), AcOH (1 mL), 60 °C.

b

Yield was determined by 1H NMR spectroscopy using mesitylene as internal standard. Parentheses represent the isolated yield. Product ratio was determined by 1H NMR spectroscopy using mesitylene as internal standard.

c

White catalyst.

d

Reaction at 25 °C.

e

Reaction at 40 °C.

f

Reaction at 80 °C. L = triphenylphosphine, L1 = acridine. BPA = BINOL−racemic phosphoric acid.