Resolution of 2-azol-1-ylsuccinic esters by enantioselective inclusion methodology

Tetrahedron: Asymmetry

Volumn 6, Issue 2, 1995, Pages 381-384

  Zaderenko, Paula ^a   López, Pilar ^a   Ballesteros, Paloma ^a   Takumi, Hideaki ^b   Toda, Fumio ^b  

^a UNIVERSIDAD NACIONAL DE EDUCACIÓN A DISTANCIA   (Spain)

^b EHIME UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

PYRAZOLE DERIVATIVE; SUCCINIC ACID DERIVATIVE;

ARTICLE; DRUG PURIFICATION; ENANTIOMER; METHODOLOGY; PRIORITY JOURNAL;

EID: 0028948019     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00019-L     Document Type: Article

References (11)

1. Synthesis and Regioselective Hydrolysis of 2-(Imidazol-1-yl)succinic Esters
2. Additionen des Pyrazols an aktivierte Mehrfachbindungen, I
3. Optical resolution of amino acid and hydroxycarboxylic acid esters by complexation with optically active host compounds: a crystallographic result
4. Structure and inclusion characteristics of (R,R)-(?)-2,3-dimethoxy-1,1,4,4-tetraphenylbutane-1,4-diol
5. Enantioselective reduction of ketones in optically active host compounds with a BH3?ethylenediamine complex in the solid state
6. Optical resolution of pantolactone by inclusion crystallization with (R, R)-(-)-trans-2,3-bis(diphenylhydroxymethyl)-1,4-dioxaspiro[4.5]decane, and crystal structure of the resulting 1:1 complex.