One catalyst for both enantiomers: Uncovering the inversion of enantioselectivity in cinchona-mediated desymmetrization of glutaric meso-anhydrides

Tetrahedron

Volumn 68, Issue 39, 2012, Pages 8311-8317

  Ivšić, Trpimir ^a   Novak, Jurica ^a   Došlić, Nada ^a   Hameršak, Zdenko ^a  

^a RUDER BO KOVI INSTITUTE   (Croatia)

Author keywords

Asymmetric synthesis; Density functional calculations; Desymmetrization; Enantioselectivity; Hydrogen bonding

Indexed keywords

3 (4 CHLORO PHENYL) PENTANEDIOIC ACID MONOBENZYL ESTER; 3 ISOBUTYL PENTANEDIOIC ACID MONOBENZYL ESTER; ACETIC ACID; ACID ANHYDRIDE; ALCOHOL; ALKALOID; BACLOFEN; CARBOXYLIC ACID; ESTER DERIVATIVE; METHANOL; PREGABALIN; QUININE; UNCLASSIFIED DRUG; XANTHENE DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL REACTION; CINCHONA; COMPLEX FORMATION; CONTROLLED STUDY; ENANTIOMER; ENANTIOSELECTIVITY; HYDROGEN BOND; METHODOLOGY; PRIORITY JOURNAL; ROOM TEMPERATURE;

CINCHONA;

EID: 84865093820     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.07.035     Document Type: Article

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