Fig. 5: Substrate scope for the reductive deoxygenation of alcohols. | Nature Communications

Fig. 5: Substrate scope for the reductive deoxygenation of alcohols.

From: Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold

Fig. 5: Substrate scope for the reductive deoxygenation of alcohols.The alternative text for this image may have been generated using AI.

Scope of di- and triarylalkane products obtained via reductive deoxygenation. Reaction conditions: 6 (1.0 equiv), 3 (0.1–5 mol%), HSiEt3 (1.1 equiv), HFIP/MeNO2 (4:1, 2.0 M in 6), room temperature, 1.5–18 h.

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