Organic Letters · 2001 · 47 citations · 19 references
Natural SciencesChemistryOrganic ChemistryOrganometallic ChemistryReaction EngineeringOrganic SynthesisOrganometallic ReactivityCleavageEther CleavageHydroxyl DeprotectionHydroxyl FunctionalizationHydroxyl Protecting GroupsMild Reaction ConditionsSelective Bond CleavageSilyl Ether Deprotection
[structure: see text]. A highly selective cleavage of MEM ethers has been achieved in high yields using CeCl3.7H2O in refluxing acetonitrile under mild and neutral reaction conditions. The method is very rapid and compatible with other hydroxyl protecting groups such as Bn, TBDPS, Ac, Me, Tr, PMB, benzylidene, THP, MOM, BOM, and NHAc present in the substrate.
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Lanthanides in organic synthesis
Michael F. Läppert · Journal of Organometallic Chemistry · 1995 · 219 citations
Organocerium compounds in synthesis
Hsing‐Jang Liu, Kak‐Shan Shia, Xiao Shang et al. · Tetrahedron · 1999 · 134 citations