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Volumn 24, Issue 5, 2013, Pages 376-378

Multicomponent reactions for the synthesis of functionalized 1,4-oxathiane-3-thiones under microwave irradiation in water

Author keywords

1,4 Oxathiane; Carbon disulfide; Nitromethane; Oxirane; Three component reaction

Indexed keywords


EID: 84877712291     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2013.03.003     Document Type: Article
Times cited : (22)

References (16)
  • 2
    • 27844539632 scopus 로고
    • New organophosphorus derivatives of p-thioxane and 2,6-dimethyl-p- thioxane with insecticidal and acaricidal activity
    • A.H. Haubein New organophosphorus derivatives of p-thioxane and 2,6-dimethyl-p-thioxane with insecticidal and acaricidal activity J. Am. Chem. Soc. 81 1959 144 148
    • (1959) J. Am. Chem. Soc. , vol.81 , pp. 144-148
    • Haubein, A.H.1
  • 3
    • 0030997133 scopus 로고    scopus 로고
    • Chemical barriers to human immunodeficiency virus type 1 (HIV-1) infection: Retrovirucidal activity of UC781, a thiocarboxanilide nonnucleoside inhibitor of HIV-1 reverse transcriptase
    • G. Borkow, J. Barnard, and T.M. Nguyen Chemical barriers to human immunodeficiency virus type 1 (HIV-1) infection: retrovirucidal activity of UC781, a thiocarboxanilide nonnucleoside inhibitor of HIV-1 reverse transcriptase J. Virol. 71 1997 3023 3030
    • (1997) J. Virol. , vol.71 , pp. 3023-3030
    • Borkow, G.1    Barnard, J.2    Nguyen, T.M.3
  • 4
    • 0030598196 scopus 로고    scopus 로고
    • Synthesis and antifungal activity of new azole derivatives containing an oxathiane ring
    • H. Miyauchi, T. Tanio, and N. Ohashi Synthesis and antifungal activity of new azole derivatives containing an oxathiane ring Bioorg. Med. Chem. Lett. 6 1996 2377 2387
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 2377-2387
    • Miyauchi, H.1    Tanio, T.2    Ohashi, N.3
  • 5
    • 33845325214 scopus 로고    scopus 로고
    • Dioxane and oxathiane nuclei: Suitable substructures for muscarinic agonists
    • A. Piergentili, W. Quaglia, and M. Giannella Dioxane and oxathiane nuclei: suitable substructures for muscarinic agonists Bioorg. Med. Chem. 15 2007 886 896
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 886-896
    • Piergentili, A.1    Quaglia, W.2    Giannella, M.3
  • 6
    • 33947470048 scopus 로고
    • Mechanisms of epoxide reactions
    • R.E. Parker, and N.S. Isaacs Mechanisms of epoxide reactions Chem. Rev. 59 1959 737 799
    • (1959) Chem. Rev. , vol.59 , pp. 737-799
    • Parker, R.E.1    Isaacs, N.S.2
  • 8
    • 0000473902 scopus 로고
    • Recent advances in the preparation and synthetic applications of oxiranes
    • A.S. Rao, S.K. Paknikar, and J.G. Kirtane Recent advances in the preparation and synthetic applications of oxiranes Tetrahedron 39 1983 2323 2367
    • (1983) Tetrahedron , vol.39 , pp. 2323-2367
    • Rao, A.S.1    Paknikar, S.K.2    Kirtane, J.G.3
  • 9
    • 85037455306 scopus 로고
    • Synthetically useful reactions of epoxides
    • J.G. Smith Synthetically useful reactions of epoxides Synthesis 1984 1984 629 656
    • (1984) Synthesis , vol.1984 , pp. 629-656
    • Smith, J.G.1
  • 10
    • 0013424516 scopus 로고
    • The discovery of the asymmetric epoxidation
    • K.B. Sharpless The discovery of the asymmetric epoxidation Chem. Br. 22 1986 38 44
    • (1986) Chem. Br. , vol.22 , pp. 38-44
    • Sharpless, K.B.1
  • 11
    • 85082943077 scopus 로고
    • Asymmetric epoxidation of allylic alcohols: The sharpless epoxidation
    • A. Pfenninger Asymmetric epoxidation of allylic alcohols: the sharpless epoxidation Synthesis 1986 1986 89 116
    • (1986) Synthesis , vol.1986 , pp. 89-116
    • Pfenninger, A.1
  • 12
    • 0000830825 scopus 로고
    • The synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcohols
    • R.M. Hanson The synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcohols Chem. Rev. 91 1991 437 475
    • (1991) Chem. Rev. , vol.91 , pp. 437-475
    • Hanson, R.M.1
  • 13
    • 77954854111 scopus 로고    scopus 로고
    • Epoxides to α-mercapto-γ-lactones via ionic liquid promoted mercaptoacetylative ring-opening-ring-closing cascade
    • R. Patel, V.P. Srivastava, and L.D.S. Yadav Epoxides to α-mercapto-γ-lactones via ionic liquid promoted mercaptoacetylative ring-opening-ring-closing cascade Synlett 2010 2010 1797 1802
    • (2010) Synlett , vol.2010 , pp. 1797-1802
    • Patel, R.1    Srivastava, V.P.2    Yadav, L.D.S.3
  • 14
    • 38949177363 scopus 로고    scopus 로고
    • A novel synthesis of γ-lactones by tandem epoxide opening-cyclization reaction mediated by samarium(II) diiodide
    • H.S. Park, D.W. Kwon, K. Lee, and Y.H. Kim A novel synthesis of γ-lactones by tandem epoxide opening-cyclization reaction mediated by samarium(II) diiodide Tetrahedron Lett. 49 2008 1616 1618
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1616-1618
    • Park, H.S.1    Kwon, D.W.2    Lee, K.3    Kim, Y.H.4
  • 15
    • 63749132620 scopus 로고    scopus 로고
    • Tin(IV) triflimidate-catalyzed cyclization of epoxy esters to functionalized d-hydroxy-c-lactones
    • S. Antoniotti, and E. Dunach Tin(IV) triflimidate-catalyzed cyclization of epoxy esters to functionalized d-hydroxy-c-lactones Tetrahedron Lett. 50 2009 2536 2539
    • (2009) Tetrahedron Lett. , vol.50 , pp. 2536-2539
    • Antoniotti, S.1    Dunach, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.