55476-04-5Relevant articles and documents
Comparison between Conventional and Nonconventional Methods for the Synthesis of Some 2-Oxazolidinone Derivatives and Preliminary Investigation of Their Inhibitory Activity Against Certain Protein Kinases
Ziane,Mazari,Safer,Sad El Hachemi Amar,Ruchaud,Baratte,Bach
, p. 1061 - 1069 (2019/09/06)
A series of propargyl and allyl carbamates were prepared directly from propargyl and allyl alcohols and phenyl or cyclohexyl isocyanate or indirectly by generating the isocyanates in situ from the corresponding Cbz-protected amines. The obtained carbamate
Versatile synthesis of quaternary 1,3-oxazolidine-2,4-diones and their use in the preparation of α-hydroxyamides
Merino, Omar,Santoyo, Blanca M.,Montiel, Luisa E.,Jiménez-Vázquez, Hugo A.,Zepeda, L. Gerardo,Tamariz, Joaquín
experimental part, p. 3738 - 3742 (2010/08/19)
A new approach to the synthesis of 1,3-oxazolidine-2,4-diones, via a two-step reaction sequence, starting from the readily available α-ketols and isocyanates, is reported. The condensation of the latter led to the key precursors 4-methylene-2-oxazolidinon
Regioselective 1,3-dipolar cycloaddition reactions of 4-methylene-2- oxazolidinones with benzonitrile oxide
Newton, Rebecca,Savage, G. Paul
, p. 432 - 437 (2008/09/21)
Substituted 4-methylene-2-oxazolidinones were prepared in two steps by cyclizing O-propargyl carbamates, which in turn were prepared from propargyl alcohols and phenyl isocyanate. The 4-methylene-2-oxazolidinones underwent a 1,3-dipolar cycloaddition reac