Intramolecular amidoalkylation of chiral imines and iminium ions: Stereoselective synthesis of anti-1,2- and -1,3-aminoalcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Enantiodivergent 1,2- and 1,3-asymmetric induction in α- and β-alkoxyimines via metal tuning and stereodifferentiation
2. The Lewis acid mediated reaction of carbamates with γ-oxygenated allyltin and its application to (±)-statine synthesis
3. Asymmetric glycine enolate aldol reactions: synthesis of cyclosporin's unusual amino acid, MeBmt
4. Asymmetric synthesis of anti-β-hydroxy-α-amino acids
5. Stereoselective Synthesis of γ-hydroxy-α-amino acids via intramolecular amidomercuration
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4. ChemInform Abstract: Intramolecular Amidoalkylation of Chiral Imines and Iminium Ions: Stereoselective Synthesis of anti-1,2- and -1,3-Amino Alcohols.;ChemInform;2010-08-17
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