Fig. 7: Synthetic extensions of catalytic reductive deoxygenation and catalyst orthogonality. | Nature Communications

Fig. 7: Synthetic extensions of catalytic reductive deoxygenation and catalyst orthogonality.

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

Fig. 7: Synthetic extensions of catalytic reductive deoxygenation and catalyst orthogonality.The alternative text for this image may have been generated using AI.

a Reductive deoxygenation of 1-adamantol and two-step ethylation of 1,3,5-trimethoxybenzene at room temperature. b Comparison of catalysts 2 and 3 in model phosphorylation and deoxygenation reactions.

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