Self-disproportionation of enantiomers of chiral, non-racemic fluoroorganic compounds: Role of fluorine as enabling element

Synthesis (Germany)

Volumn 45, Issue 2, 2013, Pages 141-152

  Sorochinsky, Alexandere E ^a,b,c   Aceña, Joséluis ^a   Soloshonok, Vadim A ^a,b  

^a UNIVERSITY OF THE BASQUE COUNTRY UPV EHU   (Spain)

^b BASQUE FOUNDATION FOR SCIENCE   (Spain)

^c INSTITUTE OF BIOORGANIC CHEMISTRY AND PETROCHEMISTRY   (Ukraine)

Author keywords

amines; amino acids; chiral recognition; chromatography; fluorine; fluorine compounds; hydroxy acids; optical purification; physicochemical phase transitions

Indexed keywords

CHIRAL RECOGNITION; DISPROPORTIONATIONS; FLUORO-ORGANIC COMPOUNDS; GENERAL ASPECTS; HYDROXY ACIDS; NON-CONVENTIONAL METHODS;

AMINES; AMINO ACIDS; CARBOXYLIC ACIDS; CHROMATOGRAPHY; DISTILLATION; ENANTIOMERS; FLUORINE; FLUORINE COMPOUNDS; PHASE TRANSITIONS; PURIFICATION; SUBLIMATION;

CHIRALITY;

ALKYL GROUP; FLUORINE; FLUOROORGANIC COMPOUND; ORGANIC COMPOUND; UNCLASSIFIED DRUG;

ACHIRAL CHROMATOGRAPHY; CHEMICAL COMPOSITION; CHEMICAL INTERACTION; CHEMICAL PHENOMENA; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRAL CHROMATOGRAPHY; CHIRALITY; CRYSTAL; CRYSTALLOGRAPHY; DEFENSE MECHANISM; DERIVATIZATION; DISTILLATION; ENANTIOMER; HYDROGEN BOND; MOLECULAR INTERACTION; PHYSICAL CHEMISTRY; PURIFICATION; RACEMIC MIXTURE; RACEMIZATION; REVIEW; SELF DISPROPORTIONATION ENANTIOMER; STATIC ELECTRICITY; SYNTHESIS;

EID: 84872189387     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1316812     Document Type: Review

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