Regioselective synthesis of deuterated analogs of the neurotoxin MPTP

Journal of Labelled Compounds and Radiopharmaceuticals

Volumn 38, Issue 3, 1996, Pages 255-262

  Mabic, Stéphane ^a   Castagnoli, Neal ^a  

^a VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY   (United States)

Author keywords

Deuteration; MPTP; Oxidation; Pyridone; Reduction

Indexed keywords

LITHIUM COMPOUNDS; REGIOSELECTIVITY;

% REDUCTIONS; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE; 2-PYRIDONES; ALKALINES; DEUTERATED ANALOGUE; DEUTERATIONS; EFFICIENT SYNTHESIS; PYRIDONES; REGIOSELECTIVE SYNTHESIS; TETRAHYDROPYRIDINES;

DEUTERIUM;

1,2,3,6 TETRAHYDRO 1 METHYL 4 PHENYLPYRIDINE; DEUTERIUM; NEUROTOXIN;

ARTICLE; CONTROLLED STUDY; DRUG SYNTHESIS; ISOTOPE LABELING;

EID: 0029921580     PISSN: 03624803     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1344(199603)38:3<255::AID-JLCR835>3.0.CO;2-0     Document Type: Article

References (12)

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