Organic & Biomolecular Chemistry · 2016 · 26 citations · 10 references
Natural SciencesChemistryGreen ChemistryOrganic ChemistrySafer Chemical SynthesisAmino Acid Protection ChemistryAmino Protecting GroupsBasic DeprotectionDeprotection Method OptimizationDeprotection StrategyProtecting Group ChemistrySelective DeprotectionSilyl Protecting Groups
A new reagent system consisting of a Lewis acid such as BF3·Et2O or Cu(OTf)2, the mild protic acid hexafluoroisopropanol and the reducing quenching agent triethylsilane was elaborated for O-, N- and S-detritylation of nucleoside, carbohydrate and amino acid derivatives. The method is compatible with acetyl, silyl, acetal and Fmoc groups.
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On the Selective Deprotection of Trityl Ethers
Graham B. Jones, George W. Hynd, Justin M. Wright et al. · The Journal of Organic Chemistry · 1999 · 48 citations
Detritylation with ytterbium triflate
Rong Jian Lu, Daipei Liu, Roger W. Giese · Tetrahedron Letters · 2000 · 35 citations