Karwowski, Boleslaw <br/><br/>
Nuclear magnetic resonance studies of the 4R and 4S diastereomers of spiroiminodihydantoin 2'-deoxyribonucleosides: absolute configuration and conformational features.  [electronic resource] 

 -  Chemical research in toxicology  Oct 2006 
 - 1357-65 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0893-228X 
<br/><br/><label>Standard No.: </label>10.1021/tx060088f  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carbon--chemistry<br/>Deoxyribonucleosides--chemistry<br/>Guanosine--analogs & derivatives<br/>Magnetic Resonance Spectroscopy<br/>Molecular Conformation<br/>Spiro Compounds--chemistry<br/>Stereoisomerism