REFERENCES
- (a) Sakakura , T. ; Choi , J. C. ; Yasuda , H. Transformation of carbon dioxide . Chem. Rev. 2007 , 107 , 2365 – 2387 ; (b) Darensbourg , D. J. Making plastics from carbon dioxide: Salen metal complexes as catalysts for the production of polycarbonates from epoxides and CO2 . Chem. Rev. 2007 , 107 , 2388 – 2410 .
- (a) Ager , D. J. ; Prakash , I. ; Schaad , D. R. 1,2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis . Chem. Rev . 1996 , 96 , 835 – 875 ; (b) Dyen , M. E. ; Swern , D. 2-Oxazolidones . Chem. Rev . 1967 , 67 , 197 – 246 .
- (a) Matsunaga , H. ; Ishizuka , T. ; Kunieda , T. Synthetic utility of five-membered heterocycles—Chiral functionalization and applications . Tetrahedron 2005 , 61 , 8073 – 8094 ; (b) Vicario , J. L. ; Badia , D. ; Carrillo , L. ; Reyes , E. ; Etxebarria , J. α-Amino acids, β-amino alcohols, and related compounds as chiral auxiliaries, ligands and catalysts in the asymmetric aldol reaction . Curr. Org. Chem . 2005 , 9 , 219 – 235 .
- (a) Mukhtar , T. A. ; Wright , G. D. Streptogramins, oxazolidinones, and other inhibitors of bacterial protein synthesis . Chem. Rev. 2005 , 105 , 529 – 542 ; (b) Renslo , A. R. ; Luehr , G. W. ; Gordeev , M. F. Recent developments in the identification of novel oxazolidinone antibacterial agents . Bioorg. Med. Chem. 2006 , 14 , 4227 – 4240 ; (c) Osa , Y. ; Hikima , Y. ; Sato , Y. ; Takino , K. ; Ida , Y. ; Hirono , S. ; Nagase , H. Convenient synthesis of oxazolidinones by the use of halomethyloxirane, primary amine, and carbonate salt . J. Org. Chem . 2005 , 70 , 5737 – 5740 , and references therein .
- (a) Miller , A. W. ; Nguyen , S. T. (Salen)chromium(III)/DMAP: An efficient catalyst system for the selective synthesis of 5-substituted oxazolidinones from carbon dioxide and aziridines. Org. Lett . 2004, 6, 2301–2304; (b) Bhanage , B. M. ; Fujita , S. ; Ikushima , Y. ; Arai , M. Synthesis of cyclic ureas and urethanes from alkylene diamines and amino alcohols with pressurized carbon dioxide in the absence of catalysts. Green Chem. 2003, 5, 340–342; (c) Shi , M. ; Shen , Y. M. Transition-metal-catalyzed reactions of propargylamine with carbon dioxide and carbon disulfide. J. Org. Chem. 2002, 67, 16–21; (d) Bhalchandra , M. B. ; Shin-ichiro , F. ; Yutaka , I. ; Masahiko , A. Non-catalytic clean synthesis route using urea to cyclic urea and cyclic urethane compounds. Green Chem. 2004, 6, 78–80; (e) Fu , Y. ; Baba , T. ; Ono , Y. Carbonylation of o-phenylenediamine and o-aminophenol with dimethyl carbonate using lead compounds as catalysts. J. Catal. 2001, 197, 91–97; (f) Liu , J. M. ; Peng , X. G. ; Liu , J. H. ; Zheng , S. Z. ; Sun , W. ; Xia , C. G. Synthesis of 2-oxazolidinones by salen-Co-complexes catalyzed oxidative carbonylation of b-amino alcohols. Tetrahedron Lett. 2007, 48, 929–932; (g) Robles-Machin , R. ; Javier , A. ; Carretero , J. C. Gold-catalyzed synthesis of alkylidene 2-oxazolidinones and 1,3-oxazin-2-ones. J. Org. Chem. 2006, 71, 5023–5026.
- (a) Fournier , J. ; Bruneau , C. ; Dixneuf , P. H. A simple synthesis of oxazolidinones in one step from carbon dioxide . Tetrahedron Lett . 1990 , 31 , 1721 – 1722 ; (b) Gu , Y. L. ; Zhang , Q. H. ; Duan , Z. Y. ; Zhang , J. ; Zhang , S. G. ; Deng , Y. Q. Ionic liquid as an efficient promoting medium for fixation of carbon dioxide: A clean method for the synthesis of 5-methylene-1,3-oxazolidin-2-ones from propargylic alcohols, amines, and carbon dioxide catalyzed by cu(I) under mild conditions . J. Org. Chem. 2005 , 70 , 7376 – 7380 ; (c) Zhang , Q. H. ; Shi , F. ; Gu , Y. L. ; Yang , J. ; Deng , Y. Q. Efficient and eco-friendly process for the synthesis of n-substituted 4-methylene-2-oxazolidinones in ionic liquids . Tetrahedron Lett. 2005 , 46 , 5907 – 5911 ; (d) Jiang , H. F. ; Zhao , J. W. ; Wang , A. Z. ; An efficient and eco-friendly process for the conversion of carbon dioxide into oxazolones and oxazolidinones under supercritical conditions . Synthesis 2008 , 5 , 763 – 769 .