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Correction: Metal-free visible-light-induced phosphorylation of unactivated alkyl iodides with white phosphorus as the P-atom source
Correction: Metal-free visible-light-induced phosphorylation of unactivated alkyl iodides with white phosphorus as the P-atom source Correction for ‘Metal-free visible-light-induced phosphorylation of unactivated alkyl iodides with white phosphorus as the P-atom source’ by Fushan Chen et al., Green Chem., 2023, 25, 6629–6634, https://doi.org/10.1039/D3GC01579C. This article is Open Access This article has not yet been cited.
Three-component coupling reaction of white phosphorus, alcohols and diaryl disulfides: a chlorine-free avenue for accessing phosphorothioates
Three-component coupling reaction of white phosphorus, alcohols and diaryl disulfides: a chlorine-free avenue for accessing phosphorothioates† Synthesis of valuable compounds directly from small and simple molecules is an area of great interest in chemical research. However, the preparation of most organophosphorus compounds from white phosphorus currently relies on inefficient, stepwise procedures that result in significant environmental pollution and poor atom economy.
Three-component coupling reaction of white phosphorus, alcohols and diaryl disulfides: A chlorine-free avenue for accessing phosphorothioates
Three-component coupling reaction of white phosphorus, alcohols and diaryl disulfides: A chlorine-free avenue for accessing phosphorothioates ynthesis of valuable compounds directly from small and simple molecules is an area of great interest in chemical research. However, the preparation of most organophosphorus compounds from white phosphorus currently relies on inefficient, stepwise procedures that result in significant environmental pollution and poor atom economy.
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