Fig. 2: Substrate scope of cycloaddition of BCBs with 3,4-dihydroisoquinolines. | Nature Communications

Fig. 2: Substrate scope of cycloaddition of BCBs with 3,4-dihydroisoquinolines.

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

Fig. 2

Conditions: A (0.1 mmol), B (0.1 mmol) in Et2O (1.0 mL) under N2 atmosphere and 5 W LED (Ī»max = 365 nm) irradiation at 10 °C, yield of isolated product. a10 W instead of 5 W. bAfter 12 h, another portion A (0.1 mmol) was added and reacted for further 12 h; c10 W LED in THF was used.

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