1Gregory W A. P-oxooxazolidinyl benzene compounds as antibacyerial agents: US 4461773[P]. 1984-07-24
2Gregory W A, Brittelli D R, Wang C L, et al. Antibacterial. synthesis and structure-activity studies of 3-aryl-2-oxazolidinones. 1. the "B"group[J]. J Med Chem, 1989, 32(8): 1673
3Barbachyn M R, Brickner S J, Hutchinson D K, et al. Substituted oxazine and thiazine oxazolidinone antimicrobials: US 5688792[P]. 1997-11-18
4Brickner S J, Hutchinson D K, Barbachyn M R, et al. Synthesis and antibacterial aciticity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant gram-positive bacterial infections[J]. J Med Chem, 1996, 39(3): 673
5Stevens D L, Dotter B, Madaras-Kelly K. A review of linezolid: the first oxazolidinone Antibiotic[J]. Expert Rev Anti Infect Ther, 2004, 2(1): 51
6Herweh J E, Kauffmann W J. 2-oxazolidones via The lithium bromide catalyzed reaction of isocyanates with epoxides in hydrocarbon solvents[J]. Tetra Lett, 1971, 12:809
7Barbachyn M R, Brickner S J. Substituted aryl and heteroary-phenyl-oxazolidinones: US 5565571[P]. 1996- 10-15
8Gregory W A, Brittelli D R, Wang C L, et al. Antibacterial synthesis and structure -activity studies of 3-aryl-2- oxazolidinones. 2. the "A"group[J]. J Med Chem, 1990, 33(9): 2569
9Yu D, Huiyuan G. Synthesis and antibacterial activity of linezolid analogues[J]. Bioorg Med Chem Lett, 2002, 12(6): 857
10Hester J J B, Nidy E G, Perricone S C. Oxazolidinone antibacterial agents having a thiocarbonyl func-tionality: US 6362189[P]. 2002-03-26