ArticleGreen chemistry : an international journal and green chemistry resource : GC2026
Deprotection of benzyl ethers
Article in Green chemistry : an international journal and green chemistry resource : GC, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Benzyl ethers are among the most robust and indispensable protecting groups in the synthesis of complex natural products and pharmaceuticals, providing effective neutralization of the reactive hydroxy group in phenols and alcohols. However, their cleavage necessitates the use of expensive catalysts, hazardous conditions, or excessive organic additives. Herein, we report a catalyst-free, photoinduced debenzylation protocol of phenolic and aliphatic ethers. By leveraging
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