Photoinduced deprotection shows high selectivity and efficiency in tetrahydropyranyl ethers under mild conditions, suggesting a versatile method for natural products.
A photoinduced deprotection of tetrahydropyranyl (THP) ethers under mild and metal‐free conditions is reported. The transformation proceeded well in good to excellent yields (up to 98%) in the presence of 0.1 mol% of BrCCl 3 . THP ethers of both aliphatic alcohols and phenols were deprotected efficiently with high selectivity. Other acid‐sensitive protecting groups (AcO, NHBoc, and ketal) were well tolerated. This convenient methodology has also been successfully extended to typical natural product scaffolds, including amino acid derivative, sugar, and cholesterol derivatives.
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Yang et al. (2025) studied this question.
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