Publication | Closed Access
Asymmetric Synthesis of 2-Amino Alcohol Derivatives from (<i>S</i>)-α-Amino Aldehydes via Chiral Acetal Templates
25
Citations
13
References
1987
Year
Opposite Stereochemistry SeriesChiral AcetalsEngineering2-Amino Alcohol DerivativesChiral Acetal TemplatesNatural SciencesDiversity-oriented SynthesisAsymmetric SynthesisAbstract TitaniumOrganic ChemistryStereoselective SynthesisChemistryPharmacologyAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract Titanium tetrachloride mediated addition of allyltrimethylsilane to chiral acetals derived from (S)-α-amino aldehydes and (+)-(2S,4S)-pentane-2,4-diol gave the anti-2-amino alcohol derivatives with considerably high diastereoselectivity. On the other hand, the same reaction by the use of acetals obtained from (−)-(2R,4R)-pentane-2,4-diol gave the products of opposite stereochemistry series as major products.
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