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Volumn 40, Issue 24, 2010, Pages 3654-3659

A facile and efficient synthesis of 3-aryloxazolidin-2-ones from isocyanates and epoxides promoted by MgI2 etherate

Author keywords

Epoxide; isocyanate; MgI2 etherate; oxazolidinone

Indexed keywords

EPOXIDE; ETHER DERIVATIVE; ISOCYANIC ACID DERIVATIVE; MAGNESIUM DERIVATIVE; OXAZOLIDINONE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 78149430863     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903470525     Document Type: Article
Times cited : (20)

References (18)
  • 2
    • 0030027833 scopus 로고    scopus 로고
    • 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
    • (b) Brickner, S. J.; Hutchinson, D. K.; Barbachyn, M. R.; Manninen, P. R.; Ulanowicz, D. A.; Garmon, S. A.; Grega, K. C.; Hendges, S. K.; Toops, D. S.; Ford, C. W.; Zurenko, G. E. 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. Med. Chem. 1996, 39, 673;
    • (1996) J. Med. Chem. , vol.39 , pp. 673
    • Brickner, S.J.1    Hutchinson, D.K.2    Barbachyn, M.R.3    Manninen, P.R.4    Ulanowicz, D.A.5    Garmon, S.A.6    Grega, K.C.7    Hendges, S.K.8    Toops, D.S.9    Ford, C.W.10    Zurenko, G.E.11
  • 4
    • 0038587681 scopus 로고    scopus 로고
    • Oxazolidinone structure-activity relationships leading to linezolid
    • (d) Barbachyn, M. R.; Ford, C. W. Oxazolidinone structure-activity relationships leading to linezolid. Angew. Chem., Int. Ed. 2003, 42, 2010.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2010
    • Barbachyn, M.R.1    Ford, C.W.2
  • 5
    • 0000634701 scopus 로고
    • Preparation of substituted 2-oxazolidones from 1,2-epoxides and isocyanates
    • Speranza, G. P.; Peppel, W. J. Preparation of substituted 2-oxazolidones from 1,2-epoxides and isocyanates. J. Org. Chem. 1958, 23, 1922.
    • (1958) J. Org. Chem. , vol.23 , pp. 1922
    • Speranza, G.P.1    Peppel, W.J.2
  • 6
    • 49649150803 scopus 로고
    • 2-Oxazolidones via the lithium bromide catalyzed reaction of isocyanates with epoxides in hydrocarbon solvents
    • Herweh, J. E.; Kauffman, W. J. 2-Oxazolidones via the lithium bromide catalyzed reaction of isocyanates with epoxides in hydrocarbon solvents. Tetrahedron Lett. 1971, 12, 809.
    • (1971) Tetrahedron Lett. , vol.12 , pp. 809
    • Herweh, J.E.1    Kauffman, W.J.2
  • 7
    • 0000084862 scopus 로고
    • Synthesis and nuclear magnetic resonance spectra of 2-oxazolidones
    • Herweh, J. E.; Foglia, T. A.; Swern, D. Synthesis and nuclear magnetic resonance spectra of 2-oxazolidones. J. Org. Chem. 1968, 33, 4029.
    • (1968) J. Org. Chem. , vol.33 , pp. 4029
    • Herweh, J.E.1    Foglia, T.A.2    Swern, D.3
  • 8
    • 0010104952 scopus 로고
    • Cycloaddition reaction of heterocumu-lenes with oxiranes catalyzed by organotin iodide-Lewis base complex
    • Shibata, I.; Baba, A.; Iwasaki, H.; Matsuda, H. Cycloaddition reaction of heterocumu-lenes with oxiranes catalyzed by organotin iodide-Lewis base complex. J. Org. Chem. 1986, 51, 2177.
    • (1986) J. Org. Chem. , vol.51 , pp. 2177
    • Shibata, I.1    Baba, A.2    Iwasaki, H.3    Matsuda, H.4
  • 10
    • 85050510929 scopus 로고
    • A facile synthesis of oxazolidinones via lanthanide - Catalyzed cycloaddition of epoxides with isocyanates
    • Qian, C.-T.; Zhu, D.-M. A facile synthesis of oxazolidinones via lanthanide - catalyzed cycloaddition of epoxides with isocyanates. Synlett. 1994, 129.
    • (1994) Synlett. , vol.129
    • Qian, C.-T.1    Zhu, D.-M.2
  • 11
    • 0347655368 scopus 로고    scopus 로고
    • The synthetic applications of Lewis acidic Mg(II)
    • Zhang, X.-X.; Li, W.-D. The synthetic applications of Lewis acidic Mg(II). Chinese J. Org. Chem. 2003, 23, 1185.
    • (2003) Chinese J. Org. Chem. , vol.23 , pp. 1185
    • Zhang, X.-X.1    Li, W.-D.2
  • 12
    • 38549159912 scopus 로고    scopus 로고
    • 2 etherate
    • 2 etherate. Synlett. 2008, 1, 65-68;
    • (2008) Synlett. , vol.1 , pp. 65-68
    • Zhang, X.-X.1
  • 14
    • 0033935920 scopus 로고    scopus 로고
    • Asymmetric catalysis of aldol reactions with chiral Lewis bases
    • (a) Denmark, S. E.; Stavenger, R. A. Asymmetric catalysis of aldol reactions with chiral Lewis bases. Acc. Chem. Res. 2000, 33, 432;
    • (2000) Acc. Chem. Res. , vol.33 , pp. 432
    • Denmark, S.E.1    Stavenger, R.A.2
  • 15
    • 0034832840 scopus 로고    scopus 로고
    • Lewis base activation of Lewis acids: Catalytic enantioselective allylation and propargylation of aldehydes
    • (b) Denmark, S. E.; Wynn, T. Lewis base activation of Lewis acids: Catalytic enantioselective allylation and propargylation of aldehydes. J. Am. Chem. Soc. 2001, 123, 6199.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 6199
    • Denmark, S.E.1    Wynn, T.2
  • 16
    • 0041857761 scopus 로고    scopus 로고
    • Samarium triiodide catalyzed cycloaddition of epoxides with isocyanates: A facile synthesis of oxazolidinones
    • Wu, H.-Y.; Ding, J.-C.; Liu, Y.-K. Samarium triiodide catalyzed cycloaddition of epoxides with isocyanates: A facile synthesis of oxazolidinones. J. Indian Chem. Soc. 2003, 80(1), 36.
    • (2003) J. Indian Chem. Soc. , vol.80 , Issue.1 , pp. 36
    • Wu, H.-Y.1    Ding, J.-C.2    Liu, Y.-K.3
  • 17
    • 84875964043 scopus 로고
    • Novel methods of preparation of 2-oxazolidones
    • Zofia, L.-Z.; Tadeusz, U. Novel methods of preparation of 2-oxazolidones. Org. Prep. Proc. Inter. 1971, 3(1), 1-4.
    • (1971) Org. Prep. Proc. Inter. , vol.3 , Issue.1 , pp. 1-4
    • Zofia, L.-Z.1    Tadeusz, U.2
  • 18
    • 37049055593 scopus 로고
    • The reaction of carbonyl chloride with 1,2-epoxides
    • Idris, J. J. The reaction of carbonyl chloride with 1,2-epoxides. J. Chem. Soc. 1957, 2735.
    • (1957) J. Chem. Soc. , vol.2735
    • Idris, J.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.