Cycloalkane-1,2-diamine derivatives as chiral solvating agents. Study of the structural variables controlling the NMR enantiodiscrimination of chiral carboxylic acids

Tetrahedron

Volumn 64, Issue 33, 2008, Pages 7709-7717

  Peña, Carmen ^a   González Sabín, Javier ^b   Alfonso, Ignacio ^c   Rebolledo, Francisca ^a   Gotor, Vicente ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

^b Entrechem SL ^*  (Spain)

^c DEPARTMENT OF ENVIRONMENTAL CHEMISTRY   (Spain)

Author keywords

Anion recognition; Chiral solvating agent (CSA); Enantiodiscrimination; NMR; Pincer

Indexed keywords

ARYLPROPIONIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CYCLOALKANE DERIVATIVE; CYCLOHEXANE 1,2 DIAMINE; CYCLOPENTANE DERIVATIVE; DIAMINE DERIVATIVE; PYRIDINE 2,6 BISCARBOXAMIDE; PYRIDINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOSELECTIVITY; HYDROGEN BOND; MOLECULAR MODEL; MOLECULAR RECOGNITION; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 46349084909     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.06.031     Document Type: Article

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