메뉴 건너뛰기




Volumn 62, Issue , 2013, Pages 534-544

Efficient synthesis of 3H,3′H-spiro[benzofuran-2,1′- isobenzofuran]-3,3′-dione as novel skeletons specifically for influenza virus type B inhibition

Author keywords

Anti influenza virus type B; Antiviral activity; Iodine; Microwave; Spiro

Indexed keywords

3H,3'H SPIROL[BEZOFURAN 2,1' ISOBENZOFURAN] 3,3' DIONE DERIVATIVE; ADAMANTANE DERIVATIVE; ANTIVIRUS AGENT; LACTONE DERIVATIVE; PROTEIN M2; SPIRO COMPOUND; UNCLASSIFIED DRUG;

EID: 84873701204     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.01.015     Document Type: Article
Times cited : (57)

References (36)
  • 1
    • 33751517736 scopus 로고    scopus 로고
    • Antiviral agents active against influenza A viruses
    • E. De Clercq Antiviral agents active against influenza A viruses Nat. Rev. Drug Discov. 5 2006 1015 1025
    • (2006) Nat. Rev. Drug Discov. , vol.5 , pp. 1015-1025
    • De Clercq, E.1
  • 2
    • 0034796387 scopus 로고    scopus 로고
    • A history of influenza
    • C.W. Potter A history of influenza J. Appl. Microbiol. 91 2001 572 579
    • (2001) J. Appl. Microbiol. , vol.91 , pp. 572-579
    • Potter, C.W.1
  • 5
    • 11144334667 scopus 로고    scopus 로고
    • Transmissibility of 1918 pandemic influenza
    • C.E. Mills, J.M. Robins, and M. Lipsitch Transmissibility of 1918 pandemic influenza Nature 432 2004 904 906
    • (2004) Nature , vol.432 , pp. 904-906
    • Mills, C.E.1    Robins, J.M.2    Lipsitch, M.3
  • 6
    • 10944240992 scopus 로고    scopus 로고
    • Influenza: Old and new threats
    • P. Palese Influenza: old and new threats Nat. Med. 10 2004 S82 S87
    • (2004) Nat. Med. , vol.10
    • Palese, P.1
  • 9
    • 82955235541 scopus 로고    scopus 로고
    • Antivirals and resistance: Influenza virus
    • M.G. Ison Antivirals and resistance: influenza virus Curr. Opin. Virol. 1 2011 563 573
    • (2011) Curr. Opin. Virol. , vol.1 , pp. 563-573
    • Ison, M.G.1
  • 13
    • 0015341695 scopus 로고
    • Psychosedative agents. 2. 8-(4-Substituted 1-peperazinylalkyl)-8-azaspiro [4.5]decane-7,9-diones
    • Y.H. Wu, J.W. Rayburn, L.E. Allen, H.C. Ferguson, and J.W. Kissel Psychosedative agents. 2. 8-(4-Substituted 1-peperazinylalkyl)-8-azaspiro [4.5]decane-7,9-diones J. Med. Chem. 15 1972 477 479
    • (1972) J. Med. Chem. , vol.15 , pp. 477-479
    • Wu, Y.H.1    Rayburn, J.W.2    Allen, L.E.3    Ferguson, H.C.4    Kissel, J.W.5
  • 14
    • 55849101803 scopus 로고    scopus 로고
    • The antipsychotic spiperone attenuates inflammatory response in cultured microglia via the reduction of proinflammatory cytokine expression and nitric oxide production
    • L.T. Zheng, J. Hwang, J. Ock, M.G. Lee, W.H. Lee, and K. Suk The antipsychotic spiperone attenuates inflammatory response in cultured microglia via the reduction of proinflammatory cytokine expression and nitric oxide production J. Neurochem. 107 5 2008 1225 1235
    • (2008) J. Neurochem. , vol.107 , Issue.5 , pp. 1225-1235
    • Zheng, L.T.1    Hwang, J.2    Ock, J.3    Lee, M.G.4    Lee, W.H.5    Suk, K.6
  • 15
    • 0031060189 scopus 로고    scopus 로고
    • Novel mammalian cell cycle inhibitors, cyclotroprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase
    • C.B. Cui, H. Kakeya, and H. Osada Novel mammalian cell cycle inhibitors, cyclotroprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase Tetrahedron 53 1997 59 72
    • (1997) Tetrahedron , vol.53 , pp. 59-72
    • Cui, C.B.1    Kakeya, H.2    Osada, H.3
  • 16
    • 0034671538 scopus 로고    scopus 로고
    • Total synthesis of (-)-spirotryprostatin B and three stereoisomers
    • L.E. Overman, and M.D. Rosen Total synthesis of (-)-spirotryprostatin B and three stereoisomers Angew. Chem. Int. Ed. Engl. 39 2000 4596 4599
    • (2000) Angew. Chem. Int. Ed. Engl. , vol.39 , pp. 4596-4599
    • Overman, L.E.1    Rosen, M.D.2
  • 19
    • 0034224397 scopus 로고    scopus 로고
    • Characterization of hole transport in a new class of spiro-linked oligotriphenylamine compounds
    • U. Bach, K.De. Cloedt, H. Spretizer, and M. Gratzel Characterization of hole transport in a new class of spiro-linked oligotriphenylamine compounds Adv. Mater. 12 2000 1060 1063
    • (2000) Adv. Mater. , vol.12 , pp. 1060-1063
    • Bach, U.1    Cloedt, K.De.2    Spretizer, H.3    Gratzel, M.4
  • 20
    • 0033597970 scopus 로고    scopus 로고
    • Stereocontrolled synthesis of spirocyclics
    • M. Sannigrahi Stereocontrolled synthesis of spirocyclics Tetrahedron 55 1999 9007 9071
    • (1999) Tetrahedron , vol.55 , pp. 9007-9071
    • Sannigrahi, M.1
  • 23
    • 37049082847 scopus 로고
    • First synthesis of spiro[benzofuran-2,1′-isobenzofuran]-3,3′- dione and its x-ray crystal structure
    • R.M. Letcher, N.C. Kwok, and K.K. Cheung First synthesis of spiro[benzofuran-2,1′-isobenzofuran]-3,3′-dione and its x-ray crystal structure J. Chem. Soc. Perkin Trans. 1 1992 1769 1771
    • (1992) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1769-1771
    • Letcher, R.M.1    Kwok, N.C.2    Cheung, K.K.3
  • 24
    • 0038538272 scopus 로고    scopus 로고
    • The synthesis of wrightiadione via directed remote metallation
    • N. Thasana, and S. Ruchirawat The synthesis of wrightiadione via directed remote metallation Synlett 7 2003 1037 1039
    • (2003) Synlett , vol.7 , pp. 1037-1039
    • Thasana, N.1    Ruchirawat, S.2
  • 25
    • 0000407254 scopus 로고    scopus 로고
    • Synthesis of spiro[2H-indole-2,1′-1H-isoindole]-3,3′-diones, spiro[1H-isobenzofuran-1,2′-2H-indole]-3,3′-diones and spiro[benzofuran-2,1′-isobenzofuran]-3,3′-diones via transannular reactions of eight membered ring intermediates
    • J.L. Bullington, and J.H. Dodd Synthesis of spiro[2H-indole-2,1′- 1H-isoindole]-3,3′-diones, spiro[1H-isobenzofuran-1,2′-2H-indole]-3, 3′-diones and spiro[benzofuran-2,1′-isobenzofuran]-3,3′-diones via transannular reactions of eight membered ring intermediates J. Heterocycl. Chem. 35 1998 397 403
    • (1998) J. Heterocycl. Chem. , vol.35 , pp. 397-403
    • Bullington, J.L.1    Dodd, J.H.2
  • 26
    • 0037458801 scopus 로고    scopus 로고
    • Ruthenium-catalyzed carbonylative cycloaddition of α-keto lactones with alkenes or alkynes: The participation of an ester-carbonyl group in cycloaddition reactions as the two-atom assembling unit
    • N. Chatani, K. Amako, M. Tobisu, T. Asaumi, Y. Fukumoto, and S. Murai Ruthenium-catalyzed carbonylative cycloaddition of α-keto lactones with alkenes or alkynes: the participation of an ester-carbonyl group in cycloaddition reactions as the two-atom assembling unit J. Org. Chem. 68 2003 1591 1593
    • (2003) J. Org. Chem. , vol.68 , pp. 1591-1593
    • Chatani, N.1    Amako, K.2    Tobisu, M.3    Asaumi, T.4    Fukumoto, Y.5    Murai, S.6
  • 27
    • 0027941199 scopus 로고
    • Reaction of ninhydrin with activated anilines: Formation of indole derivatives
    • D.St.C. Black, M.C. Bowyer, G.C. Condie, D.C. Craig, and N. Kumar Reaction of ninhydrin with activated anilines: formation of indole derivatives Tetrahedron 50 1994 10983 10994
    • (1994) Tetrahedron , vol.50 , pp. 10983-10994
    • Black, D.St.C.1    Bowyer, M.C.2    Condie, G.C.3    Craig, D.C.4    Kumar, N.5
  • 28
    • 33748502533 scopus 로고    scopus 로고
    • Novel heterocycles from 5-methyldibenz[b,f]azocin-6,12-dione and its derivatives
    • R.M. Letcher, N.C. Kwok, W.H. Lo, and K.W. Ng Novel heterocycles from 5-methyldibenz[b,f]azocin-6,12-dione and its derivatives J. Chem. Soc. Perkin Trans. 1 1998 1715 1719
    • (1998) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1715-1719
    • Letcher, R.M.1    Kwok, N.C.2    Lo, W.H.3    Ng, K.W.4
  • 29
    • 0032998544 scopus 로고    scopus 로고
    • Formation of benzo[b]indeno[2,1-d]furanone ring system during alkylation of 2-(2-hydroxyaryl)-2-hydroxy-1,3-indanedione derivatives
    • H.N. Song, M.R. Seong, H.J. Lee, and J.N. Kim Formation of benzo[b]indeno[2,1-d]furanone ring system during alkylation of 2-(2-hydroxyaryl)-2-hydroxy-1,3-indanedione derivatives Synth. Commun. 29 1999 2759 2767
    • (1999) Synth. Commun. , vol.29 , pp. 2759-2767
    • Song, H.N.1    Seong, M.R.2    Lee, H.J.3    Kim, J.N.4
  • 30
    • 0010368988 scopus 로고
    • Synthesis of tetrahydroindeno[1,2-b]indol-10-ones and their rearrangement to [2]benzopyrano[4,3-b]indol-5-ones
    • J.L. Bullington, and J.H. Dodd Synthesis of tetrahydroindeno[1,2-b]indol- 10-ones and their rearrangement to [2]benzopyrano[4,3-b]indol-5-ones J. Org. Chem. 58 1993 4833 4836
    • (1993) J. Org. Chem. , vol.58 , pp. 4833-4836
    • Bullington, J.L.1    Dodd, J.H.2
  • 33
    • 84862784565 scopus 로고    scopus 로고
    • In vitro inhibition of influenza A virus infection by marine microalga-derived sulfated polysaccharide p-KG03
    • M. Kim, J.H. Yim, S.Y. Kim, H.S. Kim, W.G. Lee, S.J. Kim, P.S. Kang, and C.K. Lee In vitro inhibition of influenza A virus infection by marine microalga-derived sulfated polysaccharide p-KG03 Antiviral Res. 93 2012 253 259
    • (2012) Antiviral Res. , vol.93 , pp. 253-259
    • Kim, M.1    Yim, J.H.2    Kim, S.Y.3    Kim, H.S.4    Lee, W.G.5    Kim, S.J.6    Kang, P.S.7    Lee, C.K.8
  • 34
    • 0023709365 scopus 로고    scopus 로고
    • A highly reliable, sensitive, flow cytometric/fluorometric assay for the evaluation of the anti-HIV activity of antiviral compounds in MT-4 cells
    • E.D. Clercq, D. Schols, R. Pauwels, F. Vanlangendonck, and J. Balzarini A highly reliable, sensitive, flow cytometric/fluorometric assay for the evaluation of the anti-HIV activity of antiviral compounds in MT-4 cells J. Immunol. Methods 114 1998 27 32
    • (1998) J. Immunol. Methods , vol.114 , pp. 27-32
    • Clercq, E.D.1    Schols, D.2    Pauwels, R.3    Vanlangendonck, F.4    Balzarini, J.5
  • 35
    • 0034491974 scopus 로고    scopus 로고
    • Inactivation of HSV-1 and HSV-2 and prevention of cell-to-cell virus spread by Santolina insularis essential oil
    • A. De Logu, G. Loy, M.L. Pellerano, L. Bonsignore, and M.L. Schivo Inactivation of HSV-1 and HSV-2 and prevention of cell-to-cell virus spread by Santolina insularis essential oil Antiviral Res. 48 2000 177 185
    • (2000) Antiviral Res. , vol.48 , pp. 177-185
    • De Logu, A.1    Loy, G.2    Pellerano, M.L.3    Bonsignore, L.4    Schivo, M.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.