55740-07-3Relevant articles and documents
A novel synthesis of N-but-3-enyl-α- and β-amino acids
Van Nguyen,Brownlee, Robert T. C.,Hughes, Andrew B.
experimental part, p. 1991 - 1998 (2010/03/24)
N-But-3-enyl-α- and β-amino acids can be prepared by cleaving 1,3-oxazolidin-5-ones and 1,3-oxazinan-6-ones in the presence of allylsilanes and boron trifluoride etherate at room temperature in good to excellent yields. Georg Thieme Verlag Stuttgart.
Mild regeneration of the carboxylic group of amino acid alkyl esters by aqueous methanolic sodium hydrogen carbonate via 5-oxazolidinones
Allevi, Pietro,Anastasia, Mario
, p. 7663 - 7665 (2007/10/03)
A simple racemization-free procedure allows the regeneration of the carboxylic acid group of amino acid alkyl esters by way of an intermediate 5-oxazolidinone which is hydrolyzed by treatment with sodium hydrogen carbonate in aqueous methanol.
Selective reductions of oxazolidinones: New protocol for diastereoselective synthesis of vicinal amino alcohols
Reddy, G. Vidyasagar,Rao, G. Venkat,Iyengar
, p. 2653 - 2656 (2007/10/03)
Selective reductions of oxazolidinones using sodium borohydride and their application to the diastereoselective synthesis of vicinal amino alcohols are described.