Organic & Biomolecular Chemistry · 2010 · 15 citations · 25 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryCombinatorial Peptide SynthesisDiversity-oriented SynthesisOrganic SynthesisPeptide ChemistryPeptidomimetic DesignRetrosynthetic AnalysisComplex Molecule SynthesisFormation Of Complex Organic MoleculesMild Reaction ConditionsPeptide-templated SynthesisPeptidomimetic Library SynthesisReaction-based Molecular DesignReagent-based Library SynthesisSmall-molecule Library Construction
We describe the development of a novel synthesis strategy that uses common reaction conditions to transform a collection of simple building blocks into complex molecules bearing a terminal difluoromethyl group. The core of this approach is the conscious design and synthesis of new difluorinated building blocks which contain inactive and reactive groups on each side of the CF(2) group. The strategy is illustrated by application to the synthesis of CF(2)H-bearing pseudopeptides via Ugi reaction.
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George A. Olah, Masatomo Nojima, I. KEREKES · Journal of the American Chemical Society · 1974 · 113 citations