Fig. 3: Substrate scope of asymmetric cycloaddition of BCBs and benzosulfonimides. | Nature Communications

Fig. 3: Substrate scope of asymmetric cycloaddition of BCBs and benzosulfonimides.

From: Aza-[4 + 2]-cycloaddition of benzocyclobutenones into isoquinolinone derivatives enabled by photoinduced regio-specific C–C bond cleavage

Fig. 3

Conditions: A (2.0 equiv), D (0.1 mmol), Ni(NTf2)2/L3-PisEPh (1.2:1, 10 mol%) and 3 Å MS (25 mg) in CH2Cl2 (3.0 mL) at 10 °C under N2 atmosphere and irradiation (20 W LED, Ī»max = 365 nm). Yield of isolated product. Ee was determined by UPC2.

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