Synthetic Communications · 1998 · 38 citations · 20 references
EngineeringBiochemistryVersatile MethodNatural SciencesMild MethodOrganic ChemistryTheir DetetrahydropyranylationDifferent PhChemistryStereoselective SynthesisUseful Alternative TetrahydropyranylationNatural Product SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract An efficient and mild method for tetrahydropyranylation of alcohols and their detetrahydropranylation using NH4Cl is described. This protocol provides a useful alternative tetrahydropyranylation of alcohols and their deprotection at different pH.
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Protective groups in organic synthesis
Philip Hodge · Polymer · 1992 · 2.2K citations
Karel F. Bernady, M. Brawner Floyd, John F. Poletto et al. · The Journal of Organic Chemistry · 1979 · 169 citations
Novel Reagent, Lithium Trans-1-alkenyltrialkylalanate Reagents, Altmetric Attention Score +9