Štambaský, Jan <br/><br/>
A modular approach to aryl-C-ribonucleosides via the allylic substitution and ring-closing metathesis sequence. a stereocontrolled synthesis of all four α-/β- and D-/L-C-nucleoside stereoisomers.  [electronic resource] 

 -  The Journal of organic chemistry  Oct 2011 
 - 7781-803 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1520-6904 
<br/><br/><label>Standard No.: </label>10.1021/jo201110z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alkenes--chemistry<br/>Carbonates--chemistry<br/>Catalysis<br/>Chemistry Techniques, Synthetic--methods<br/>Hydroxylation<br/>Iridium--chemistry<br/>Oxygen--chemistry<br/>Rhodium--chemistry<br/>Ribonucleosides--chemical synthesis<br/>Stereoisomerism<br/>Substrate Specificity