A chiral ketone for enantioselective recognition of 1,2-amino alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
1. Chiral Recognition of Cinchona Alkaloids at the Minor and Major Grooves of 1,1'-Binaphthyl Receptors
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3. Enantioselective Recognition by a New Chiral Stationary Phase at the Receptor Level
4. Bioinspired Chemical Inversion of l-Amino Acids to d-Amino Acids
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1. Naphthalimide-Based Chiral Fluorescence Sensor Employing (S)-BINOL Unit for Highly Enantioselective Recognition of α-Amino Alcohols with Opposite Chiral Selectivity;ChemistrySelect;2018-03-22
2. Resonance-Assisted Hydrogen Bonding as a Driving Force in Synthesis and a Synthon in the Design of Materials;Chemistry - A European Journal;2016-08-05
3. A Novel Dimeric BINOL for Enantioselective Recognition of 1,2-Amino Alcohols;Chinese Journal of Chemistry;2014-09-15
4. Highly Enantioselective Extraction of Underivatized Amino Acids by the Uryl-Pendant Hydroxyphenyl-Binol Ketone;Chemistry - A European Journal;2014-02-02
5. Enantiomeric differentiation of β-amino alcohols under electrospray ionization mass spectrometric conditions;Journal of Mass Spectrometry;2014-01
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