Crossref
journal-article
Elsevier BV
Tetrahedron (78)
References
71
Referenced
83
- As representative examples see:
10.1002/anie.200200528
/ Angew. Chem., Int. Ed. by Barbachyn (2003)10.1074/jbc.M302109200
/ J. Biol. Chem. by Colca (2003)10.1128/AAC.47.3.1148-1150.2003
/ Antimicrob. Agents Chemother. by Hoellman (2003)10.1128/AAC.47.6.1824-1831.2003
/ Antimicrob. Agents Chemother. by Rubinstein (2003)10.1093/jac/dkf109
/ J. Antimicrob. Chemother. by Fluit (2002)- As representative examples using oxazolidinones as chiral auxiliaries, see:
10.1016/S0957-4166(99)00384-5
/ Tetrahedron: Asymmetry by Prashad (1999)10.1016/S0957-4166(02)00043-5
/ Tetrahedron: Asymmetry by Gawley (2002)10.1016/S0040-4039(98)00230-5
/ Tetrahedron Lett. by Phoon (1998)- As representative examples using oxazolidinones as intermediates, see:
10.1021/cr030110z
/ Chem. Rev. by Makhtar (2005)10.1021/cr030024z
/ Chem. Rev. by Aurelio (2004)10.1081/SCC-200034770
/ Synth. Commun. by Shi (2004)10.1021/ol051200o
/ Org. Lett. by Andreou (2005)10.1016/S0040-4039(01)02151-7
/ Tetrahedron Lett. by Watson (2002)10.1021/ja01600a042
/ J. Am. Chem. Soc. by Ben-Ishai (1956)10.1021/op034033l
/ Org. Process Res. Dev. by Vo (2003)10.1021/ja01145a035
/ J. Am. Chem. Soc. by Close (1951)- Lynn, J. W. U.S. Patent 2,975,187, 1961;
-
Steele, A. B. U.S. Patent 2,868,801, 1959;
(
10.1136/bmj.2.5156.868
) 10.1080/03086648808079708
/ Phosphorus Sulfur Silicon Relat. Elem. by Yoshida (1988)10.1039/cc9960001699
/ Chem. Commun. by Costa (1996)10.1021/jo0014966
/ J. Org. Chem. by Shi (2002)10.1021/jo0511804
/ J. Org. Chem. by Feroci (2005)10.1021/jo050802i
/ J. Org. Chem. by Gu (2005)- The cycloaddition of CO2 and aziridines to give oxazolidinones, see:
10.1021/ol049689t
/ Org. Lett. by Miller (2004)10.1002/ejoc.200400083
/ Eur. J. Org. Chem. by Shen (2004)10.1016/S0040-4039(03)01325-X
/ Tetrahedron Lett. by Hancock (2003)10.1016/j.tetlet.2003.12.052
/ Tetrahedron Lett. by Sudo (2004)10.1016/j.tetlet.2003.09.011
/ Tetrahedron Lett. by Sudo (2003)10.1016/S0040-4039(02)00676-7
/ Tetrahedron Lett. by Kawanami (2002)10.1246/cl.2005.60
/ Chem. Lett. by Kawanami (2005)10.1039/a910285j
/ Chem. Commun. by Tascedda (2000)10.1002/anie.200352215
/ Angew. Chem., Int. Ed. by Ihata (2004)10.1021/ma050549o
/ Macromolecules by Ihata (2005)10.1021/jo800269v
/ J. Org. Chem. by Du (2008)10.1021/jo020191j
/ J. Org. Chem. by Shen (2003)10.2174/1385272033486693
/ Curr. Org. Chem. by Shi (2003){'key': '10.1016/j.tet.2009.05.034_bib8', 'series-title': 'Speciality Inorganic Chemicals', 'author': 'Farnworth', 'year': '1980'}
/ Speciality Inorganic Chemicals by Farnworth (1980)10.1081/SCC-200058005
/ Synth. Commun. by Shirini (2005)10.1002/ejoc.200400921
/ Eur. J. Org. Chem. by Shi (2005)10.1016/j.tetlet.2004.10.164
/ Tetrahedron Lett. by Ghosh (2005)10.1039/b504369g
/ Green Chem. by Mantri (2005)10.1002/adsc.200404149
/ Adv. Synth. Catal. by Nakayama (2004)10.3390/11040263
/ Molecules by Sun (2006)10.1016/j.molcata.2005.11.025
/ Mol. Catal. A: Chem. by Firouzabadi (2006)10.1016/j.tetlet.2007.06.104
/ Tetrahedron Lett. by Rodriguez-Dominguez (2007)10.1002/ejoc.200600493
/ Eur. J. Org. Chem. by Eftekhari-Sis (2006)10.1002/hc.20191
/ Heteroat. Chem. by Moghaddam (2006)10.1016/j.catcom.2006.06.003
/ Catal. Commun. by Mohammad poor-Baltork (2007)10.1016/j.catcom.2007.02.020
/ Catal. Commun. by Mohammadpoor-Baltork (2007)10.1016/j.catcom.2006.10.022
/ Catal. Commun. by Zhang (2007)10.1016/j.tet.2006.02.037
/ Tetrahedron by Ghosh (2006)10.1016/j.catcom.2007.01.015
/ Catal. Commun. by Zhang (2007)10.1021/jo8009006
/ J. Org. Chem. by Bhagat (2008)10.1016/j.tetlet.2008.04.084
/ Tetrahedron Lett. by Shen (2008)10.1002/anie.200701467
/ Angew. Chem. Int. Ed. by Xie (2007)10.1016/j.micromeso.2007.07.006
/ Micropor. Mesopor. Mat. by Benaliouche (2008)10.1016/j.molcata.2008.06.012
/ Mol. Catal. A: Chem. by Oliveira (2008)10.1021/ja00185a023
/ J. Am. Chem. Soc. by Calet (1989)10.1107/S0365110X56001558
/ Acta Crystallogr. by Clearfield (1956)10.1021/ol051412l
/ Org. Lett. by Capriati (2005)10.1002/ejoc.200400253
/ Eur. J. Org. Chem. by Chakraborti (2004)10.1021/jo00295a053
/ J. Org. Chem. by Chamchaang (1990)10.1021/ja00185a023
/ J. Am. Chem. Soc. by Calet (1989)10.1021/jm00312a004
/ J. Med. Chem. by Bergmann (1968)10.1021/jo01275a007
/ J. Org. Chem. by Herweh (1968)10.1080/00397918808060874
/ Synth. Commun. by Das (1988)10.1021/jo060612n
/ J. Org. Chem. by Orito (2006)
@article{Wu_2009, title={Zirconyl chloride: an efficient recyclable catalyst for synthesis of 5-aryl-2-oxazolidinones from aziridines and CO2 under solvent-free conditions}, volume={65}, ISSN={0040-4020}, url={http://dx.doi.org/10.1016/j.tet.2009.05.034}, DOI={10.1016/j.tet.2009.05.034}, number={31}, journal={Tetrahedron}, publisher={Elsevier BV}, author={Wu, Ying and He, Liang-Nian and Du, Ya and Wang, Jin-Quan and Miao, Cheng-Xia and Li, Wei}, year={2009}, month=aug, pages={6204–6210} }