Preparation of 25,26,26,26,27,27,27-heptafluoro-15-ketosterols labeled at C-23 with deuterium or tritium

Journal of Labelled Compounds and Radiopharmaceuticals

Volumn 41, Issue 1, 1998, Pages 63-74

  Su, Xiangdong ^a   Siddiqui, Abdul ^a   Swaminathan, Shankar ^a   Wilson, William K ^a   Schroepfer, George J ^a  

^a RICE UNIVERSITY   (United States)

Author keywords

15 oxygenated sterols; Deiodination; Mechanism; Stereoselectivity

Indexed keywords

ALCOHOLS; CHAINS; LIPIDS; SPECTRUM ANALYSIS; TRITIUM;

% REDUCTIONS; 15-OXYGENATED STEROL; DEIODINATION; MASS-SPECTRAL ANALYSIS; RADIOCHEMICAL PURITY; SIDE-CHAINS; SPECIFIC ACTIVITY; TRIBUTYL TIN; TRITIDES; TRITIUM ATOMS;

DEUTERIUM;

15,26,26,26,27,27,27 HEPTAFLUORO 5ALPHA CHOLEST 8(14) EN 15 ONE DERIVATIVE; 3BETA HYDROXY 15,26,26,26,27,27,27 HEPTAFLUORO 5ALPHA CHOLEST 8(14) EN 15 ONE; STEROL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DEIODINATION; DEUTERON NUCLEAR MAGNETIC RESONANCE; DRUG PURITY; ISOTOPE LABELING; MASS SPECTROMETRY; STEREOCHEMISTRY; STEROL SYNTHESIS;

TRITIUM;

EID: 0031964031     PISSN: 03624803     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1344(199801)41:1<63::AID-JLCR54>3.0.CO;2-G     Document Type: Article

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12. 3H]-4.
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21. 3H of the sodium borotritide used in these studies were those provided by the commercial supplier.