Cinchona alkaloids as privileged chiral solvating agents for the enantiodiscrimination of N-protected aminoalkanephosphonates-a comparative NMR study

Tetrahedron Asymmetry

Volumn 20, Issue 23, 2009, Pages 2709-2714

  Rudzińska, Ewa ^a   Berlicki, Łukasz ^a   Kafarski, Paweł ^a   Lämmerhofer, Michael ^b   Mucha, Artur ^a  

^a WROCLAW UNIVERSITY OF TECHNOLOGY   (Poland)

^b UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

1 (1 NAPHTHYL)ETHYLAMINE; 9 O TERT BUTYLCARBAMOYLQUINIDINE; 9 O TERT BUTYLCARBAMOYLQUININE; AMINOALKANEPHOSPHONATE DERIVATIVE; CINCHONA ALKALOID; CYCLODEXTRIN DERIVATIVE; EPHEDRINE; PHOSPHONIC ACID DERIVATIVE; QUINIDINE; QUININE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOMER; ENANTIOSELECTIVITY; HYDROGEN BOND; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 76449121235     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.11.003     Document Type: Article

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