Publication | Closed Access
Straightforward Synthesis of Novel Enantiopure α-Trifluoromethylated Azetidine 2-Carboxylic Acid and Homoserines
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Citations
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References
2015
Year
Key StepAsymmetric CatalysisEngineeringNatural SciencesDiversity-oriented SynthesisOrganic ChemistryStraightforward SynthesisStrecker-type ReactionStereoselective SynthesisChemistryPharmacologyCondensation ReactionSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The straightforward syntheses of enantiopure (2R)-2-trifluoromethyl-2-carboxyazetidine and (R)- and (S)-trifluoromethylhomoserines are reported. The key step is a Strecker-type reaction on a common chiral CF3-containing bicyclic oxazolidine intermediate obtained by a condensation reaction of (R)-phenylglycinol and ethyl-4,4,4-trifluoroacetoacetate (ETFAA).
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