Soloshonok, Vadim A <br/><br/>
Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity.  [electronic resource] 

 -  Journal of the American Chemical Society  Nov 2005 
 - 15296-303 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-7863 
<br/><br/><label>Standard No.: </label>10.1021/ja0535561  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Catalysis<br/>Glycine--chemistry<br/>Kinetics<br/>Models, Chemical<br/>Molecular Structure<br/>Nickel--chemistry<br/>Oxazolidinones--chemistry<br/>Pyrrolidonecarboxylic Acid--chemistry<br/>Schiff Bases--chemistry<br/>Spectrometry, Mass, Fast Atom Bombardment<br/>Stereoisomerism