A facile and regiospecific tritiation of sphingosine: Synthesis of (2S,3R,4E)‐2‐amino‐4‐octadecene‐1,3‐diol‐1‐3H

Journal of Labelled Compounds and Radiopharmaceuticals

Volumn 29, Issue 5, 1991, Pages 567-574

  Toyokuni, Tatsushi ^a   Nisar, Mohammad ^a   Dean, Barbara ^a   Hakomori, Sen‐Itiroh ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

deuterium; N,N,N trimethylsphingosine; N,N dimethylsphingosine; sphingosine; tritium

Indexed keywords

ENZYME INHIBITOR; N,N DIMETHYLSPHINGOSINE; SPHINGOSINE; TRITIUM;

ARTICLE; ISOTOPE LABELING; NUCLEAR MAGNETIC RESONANCE;

TRITIUM;

EID: 0025771961     PISSN: 03624803     EISSN: 10991344     Source Type: Journal    
DOI: 10.1002/jlcr.2580290508     Document Type: Article

References (31)

1. Synthesis of dl-erythro and threo-sphingosine-4,5-3H
2. The Oxidation of Primary Trimethylsilyl Ethers to Aldehydes - a selective conversion of a primary hydroxy group into an aldehyde group in the presence of a secondary hydroxy group
3. Introduction of A new Selective Oxidation Procedure Into Carbohydrate Chemistry - An Efficient Conversion of D-Galactose Into L-Fucose