[6] DixitP.P.,Nair P.S.,Patilv.J.,da1.,Synthesis and antibacterial&Medicinal Chemistry Letters[J],2005,15(12):3002-3005
[7] SelvakumarN., Reddy B. Y ., KumarGS., et a1.,Synthesis of novel tricyclic Oxazolidinones by a tandem SN2 and SNAr reaction:SAR studies on conformationlly constrained analogues of linezolid.Bioorganic&Medicinal Chemistry Letters[J], 2006,16(16): 4416—4419
[8] BorboneS., Lupo A., mezzatestaM.L., eta1., Evaluation of the invitro activity of tigecycline against multiresistant Gram-positive cocci containing tetracycline resistance determinants, International Journal of Antimicrobial Agents[J], 2008.3l(3): 209—215
[9]卢诗超. 新型抗菌药利奈唑酮的汇聚式合成. 天津大学硕士学位论文[J], 2009.
[10]朱峰, 于清新. 去甲万古霉素治疗耐药葡萄球菌严重感染的[J]. 中华医学杂志, 1992年.
[11]许巧巧, 吕伟行. 利奈唑胺导致血小板减少的危险因素分析[J]. 海峡药学, 2012年.
[12]王玉颖, 王镇山. MRSA对万古霉素、 替考拉宁和利奈唑胺体外诱导耐药性比较. 大连医科大学学报[J], 2012年.
[13] Bozdogan B. , Peter C. A. , Oxazolidinones: activity,mode of action, and mechanism of resistance, International Journal of Antimicrobial Agents[J], 2004, 23(2): 113-119
[14] D’Andrea S. , Zheng Z.B., DenBleyker K., et a1.,Synthesis and antibacterial activity of dihydro-1,2-oxazine and2-pyrazoline oxazolidinones:novel analogs of linezolid.Biooraganic& Medicinal Chemistry Letters[J], 2005, 15(211): 2834• 2839
[15] Patel Robin, Piper, Kerryl E., Rouse, Mark S., Steckelberg, James M. Linezolid therapy of Staphylococcus aureus experimental osteomyelitis. Antimicrob. Agents Chemother[J]. 2000, 44(12): 3438-3440.
[16] Stevens, Dennis L., Smith, Leon G., Bruss, Jon B., McConnell-Martin, Maureen A., Duvall, Sue E., Todd, Wesley Mark, Hafkin, Barry. Agents Chemother[J]. 2000, 44(12): 3408-3413.
[16]逄晓云, 沈金芳. 对乙酰氨基酚过量致急性肝衰竭1例[J]. 药物流行病学杂志, 2009年.
[17]杨燕, 尤启冬. 噁唑烷酮类抗菌剂构效关系及结构改造研究进展[J]. 药学进展, 2010年.
[18]丁淑芬, 王建忠. 抗菌药的分类. 中国医刊[J], 2007年.
[19]余德胜, 王志谦, 熊莺, 赵燕芳. 利奈唑酮合成新工艺[J]. 中国药物化学杂志, 2005年
[20]Brickner SJ, Hutchinson DK, Barbachyn MR. .Synthesis and antibacterial activity 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): 673-679;
[21]LOHRAY B B, BASKARAN B . A short synthesis of oxazolidinone derivatives linezolid and eperezolid: a new class of antibacteriais[ J]. Tetrahedron Lett., 1999, 40( 26): 4855- 4856.
[22] Moran RR, Liz R, Gotor V. Regioselective and stereospecific synthesis of enantiopure 1,3-oxazolidin-2-ones by intramolecular ring opening of 2-(Bocaminomethyl)aziridines.preparation of the antibiotic linezolid [J]. Org Lett. 2008, 10(10): 1935-1938;
[23] Immordino RJ, Perrault WR, Reeder MR. Process for preparing linezolid: WO,2007116284 [P]. 2007-10-18. (CA2007,147: 469356);
[24] 杨燕, 尤启东. 噁唑烷酮类抗菌剂构效关系及结构改造研究进展 [J]. 药学进展,2010, 34(11): 481-490. [25] Bhardwaj, V., Gumber D., Abbot, V., Dhiman, S., Sharma P., Pyrrole: a resourceful small molecule in key medicinal hetero-aromatics [J]. RSC Adv., 2015, 5: 15233-15266. 利奈唑胺的合成文献综述和参考文献(2):http://www.751com.cn/wenxian/lunwen_32892.html