More research is needed about (S)-[1,1′-Binaphthalene]-2,2′-diol

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LiI/TBHP Mediated Oxidative Cross-Coupling of P(O)?H Compounds with Phenols and Various Nucleophiles: Direct Access to the Synthesis of Organophosphates

An efficient and mild method for the direct phosphorylation of phenols, alcohols, and amines with P(O)?H has been reported by LiI/TBHP mediated oxidative cross-coupling reaction. Moreover, this protocol extended to beta-keto esters for the synthesis of enol phosphates using H-phosphonates. Notably, this developed method applied for the synthesis of organopesticides such as paraoxon, cyanophos, and methyl parathion. The key features of this protocol are mild conditions, short reaction time, good functional group tolerance, and broad substrate scope.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 18531-99-2, help many people in the next few years.name: (S)-[1,1′-Binaphthalene]-2,2′-diol

Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI