97899-38-2Relevant articles and documents
Synthesis of Oxazolidinones by a Hypervalent Iodine Mediated Cyclization of N-Allylcarbamates
Das, Mirdyul,Rodríguez, Arantxa,Lo, Pui Kin Tony,Moran, Wesley J.
, p. 1646 - 1650 (2021/02/11)
The preparation of oxazolidinones by the hypervalent iodine mediated cyclization of allylcarbamates is described. A versatile range of substrates can be converted into substituted oxazolidinones primed for further transformations. Derivatization of the products at both ends is demonstrated. A preliminary attempt at the enantioselective formation of an oxazolidinone using a chiral iodane is also presented. (Figure presented.).
Synthesis and Antimicrobial Activity of Oxazolidin-2-ones and Related Heterocycles
Seneci, Pierfausto,Caspani, Marco,Ripamonti, Franca,Ciabatti, Romeo
, p. 2345 - 2352 (2007/10/02)
A series of 5-membered heterocycles, structurally related to the known antibacterial oxazolidin-2-ones 1, have been prepared by modifying the model compound 1a at the 1-, 2-, 2'- and 3-positions.The antibacterial activity of compound 1a was strongly affec