Development of metallocomplex amino acids synthons for the asymmetric preparation of α-amino acids by stereoselective introduction of a side chain. Evaluation of the model asymmetric preparation of alanine and β-13C monolabelled a-aminoisobutyric acid

Journal of Radioanalytical and Nuclear Chemistry

Volumn 285, Issue 3, 2010, Pages 621-626

  Popkov, Alexander ^d   Hanusek, Jiří ^a   Cermak, Jiří ^b   Langer, Vratislav ^c   Jirásko, Robert ^a   Holčapek, Michal ^a   Nádvorník, Milan ^a  

^a UNIVERSITY OF PARDUBICE   (Czech Republic)

^b Vyzkumny ustav organickych syntez as   (Czech Republic)

^c CHALMERS UNIVERSITY OF TECHNOLOGY   (Sweden)

^d NONE

Author keywords

6 18F FDOPA; Amino acids; Nickel; PET; Schiff bases; Stereoselectivity

Indexed keywords

2 AMINO 2 METHYLPROPIONIC ACID; 2 METIROSINE F 18; 6 ALPHA METHYLDOPAMINE F 18; 6 FLUORODOPAMINE F 18; ALANINE; ALPHA AMINO ACID; FLUORINE 18; GLYCINE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CONTROLLED STUDY; EPIMERIZATION; METHYLATION; POSITRON EMISSION TOMOGRAPHY; RADIOCHEMISTRY; STEREOCHEMISTRY; THERMODYNAMICS;

EID: 77957868086     PISSN: 02365731     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10967-010-0578-5     Document Type: Article

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