메뉴 건너뛰기




Volumn 27, Issue 8, 2008, Pages 992-1000

Mineral supported facile synthesis of novel 4-hydroxybenzoxazin-2-thione N-nucleosides

Author keywords

Benzoxazin 2 thione N nucleosides; Microwaves; Mineral supported; One pot; Solvent free; Substituted salicylaldehyde

Indexed keywords

ALDEHYDE; MINERAL; MONTMORILLONITE; NUCLEOSIDE DERIVATIVE; SALICYLALDEHYDE; SOLVENT; THIOUREA DERIVATIVE;

EID: 49549120635     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770802258042     Document Type: Article
Times cited : (9)

References (27)
  • 3
    • 0033972803 scopus 로고    scopus 로고
    • The herpesvirus proteases as targets for antiviral chemotherapy
    • Waxman, L.; Darke, P.L. The herpesvirus proteases as targets for antiviral chemotherapy. Antivir. Chem. Chemother, 2000, 11, 1-22.
    • (2000) Antivir. Chem. Chemother , vol.11 , pp. 1-22
    • Waxman, L.1    Darke, P.L.2
  • 4
    • 0041999579 scopus 로고    scopus 로고
    • Synthesis of novel 3-acyloxy-1,3-dihydro-2H-indol-2-ones and isomeric 4-acyl-1,4-dihydro-3,1- benzoxazin-2-ones: Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones
    • Klasek, A.; Koristek, K.; Polis, J.; Kosmrlj, J. Synthesis of novel 3-acyloxy-1,3-dihydro-2H-indol-2-ones and isomeric 4-acyl-1,4-dihydro-3,1- benzoxazin-2-ones: Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones. Tetrahedron 2000, 56, 1551-1560.
    • (2000) Tetrahedron , vol.56 , pp. 1551-1560
    • Klasek, A.1    Koristek, K.2    Polis, J.3    Kosmrlj, J.4
  • 5
    • 0022653365 scopus 로고
    • The antiviral potential of compounds containing the thiophosphoryl group
    • Hutchinson, D.W.; Masson, S. The antiviral potential of compounds containing the thiophosphoryl group. I. R. C. S. Med. Sc. 1986, 14, 176-177.
    • (1986) I. R. C. S. Med. Sc , vol.14 , pp. 176-177
    • Hutchinson, D.W.1    Masson, S.2
  • 6
    • 0025633915 scopus 로고
    • Synthesis and antiviral activity of the 3-deaza analogue of 9-[(1,3-dihydroxy-2-propoxy) methyl]-guanine
    • McGee, D.P.C.; Martin, J.C.; Smee, D.F.; Verheyden, J.P.H. Synthesis and antiviral activity of the 3-deaza analogue of 9-[(1,3-dihydroxy-2-propoxy) methyl]-guanine. Nucleosides Nucleotides 1990, 9, 815-826.
    • (1990) Nucleosides Nucleotides , vol.9 , pp. 815-826
    • McGee, D.P.C.1    Martin, J.C.2    Smee, D.F.3    Verheyden, J.P.H.4
  • 7
    • 0028757621 scopus 로고
    • Multi-component reactions in organic chemistry
    • Ugi, I.; Domling, A. Multi-component reactions in organic chemistry. Endeavour 1994, 18, 115-122.
    • (1994) Endeavour , vol.18 , pp. 115-122
    • Ugi, I.1    Domling, A.2
  • 8
    • 0039944586 scopus 로고    scopus 로고
    • A versatile multi-component one-pot thiazole synthesis
    • Heck, S.; Domling, A. A versatile multi-component one-pot thiazole synthesis. Synlett 2000, 424-426.
    • (2000) Synlett , pp. 424-426
    • Heck, S.1    Domling, A.2
  • 9
    • 0001277768 scopus 로고
    • The synthesis of amino acids by 1,3-dipolar cycloaddition of azomethine ylides
    • Kraus, G.A.; Nagy, J.O. The synthesis of amino acids by 1,3-dipolar cycloaddition of azomethine ylides. Tetrahedron 1985, 41, 3537-3545.
    • (1985) Tetrahedron , vol.41 , pp. 3537-3545
    • Kraus, G.A.1    Nagy, J.O.2
  • 10
    • 0033538596 scopus 로고    scopus 로고
    • Passerini and Ugi reactions of benzyl and acetyl protected isocyanoglucoses
    • Zeigler, T.; Kaisers, H.J.; Schlomer, R.; Koch, C. Passerini and Ugi reactions of benzyl and acetyl protected isocyanoglucoses. Tetrahedron 1999, 55, 8397-8408.
    • (1999) Tetrahedron , vol.55 , pp. 8397-8408
    • Zeigler, T.1    Kaisers, H.J.2    Schlomer, R.3    Koch, C.4
  • 11
    • 0029078472 scopus 로고
    • Microwave assisted organic reactions
    • Caddick, S. Microwave assisted organic reactions. Tetrahedron 1995, 51, 10403-10432.
    • (1995) Tetrahedron , vol.51 , pp. 10403-10432
    • Caddick, S.1
  • 13
    • 0033516602 scopus 로고    scopus 로고
    • Solvent-free synthesis of N-sulfonylimines using microwave irradiation
    • Varma, R.S.; Vass, A.; Dudas, J.; Solvent-free synthesis of N-sulfonylimines using microwave irradiation. Tetrahedron Lett. 1999, 40, 4951-4954.
    • (1999) Tetrahedron Lett , vol.40 , pp. 4951-4954
    • Varma, R.S.1    Vass, A.2    Dudas, J.3
  • 14
    • 0035813244 scopus 로고    scopus 로고
    • Microwave assisted organic synthesis - A review
    • Lidstrom, P.; Tierney, J.; Wathey, B.; Westman, J. Microwave assisted organic synthesis - A review. Tetrahedron 2001, 57, 9225-9283.
    • (2001) Tetrahedron , vol.57 , pp. 9225-9283
    • Lidstrom, P.1    Tierney, J.2    Wathey, B.3    Westman, J.4
  • 15
    • 0035813242 scopus 로고    scopus 로고
    • A tentative rationalization of microwave effects in organic synthesis according to the reaction medium, and mechanistic considerations
    • Perreux, L.; Loupy, A. A tentative rationalization of microwave effects in organic synthesis according to the reaction medium, and mechanistic considerations. Tetrahedron 2001, 57, 9199-9223.
    • (2001) Tetrahedron , vol.57 , pp. 9199-9223
    • Perreux, L.1    Loupy, A.2
  • 17
    • 0002650452 scopus 로고    scopus 로고
    • Liquid phase oxidations using novel surface functionalised silica supported metal catalysts
    • Chisem, J.; Chisem, I.C.; Rafelt, J.S.; Macquarrie, D.J.; Clark, J.H. Liquid phase oxidations using novel surface functionalised silica supported metal catalysts. Chem. Commun. 1997, 2203-2204.
    • (1997) Chem. Commun , pp. 2203-2204
    • Chisem, J.1    Chisem, I.C.2    Rafelt, J.S.3    Macquarrie, D.J.4    Clark, J.H.5
  • 18
    • 0033800375 scopus 로고    scopus 로고
    • Clay catalyzed facile cyclodehydration under microwave: Synthesis of 3-substituted benzofurans
    • Meshram, H.M.; Sekhar, K.C.; Ganesh, Y.S.S.; Yadav, J.S. Clay catalyzed facile cyclodehydration under microwave: synthesis of 3-substituted benzofurans. Synlett 2000, 1273-1275.
    • (2000) Synlett , pp. 1273-1275
    • Meshram, H.M.1    Sekhar, K.C.2    Ganesh, Y.S.S.3    Yadav, J.S.4
  • 19
    • 0242439426 scopus 로고    scopus 로고
    • Synthesis and fungicidal activity of novel 4,4′-bis(2″-aryl-5″-methyl/ unsubstituted-4″-oxo-thiazolidin-3″-yl) bibenzyl
    • Siddiqui, I.R.; Singh, P.K.; Singh, J.; Singh, J. Synthesis and fungicidal activity of novel 4,4′-bis(2″-aryl-5″-methyl/ unsubstituted-4″-oxo-thiazolidin-3″-yl) bibenzyl. J. Agri. Food Chem. 2003, 51, 7062-7065.
    • (2003) J. Agri. Food Chem , vol.51 , pp. 7062-7065
    • Siddiqui, I.R.1    Singh, P.K.2    Singh, J.3    Singh, J.4
  • 20
    • 7644223448 scopus 로고    scopus 로고
    • Three-component solvent-free diastereoselective formation of oxo-thiazolidinylthiazoles under microwave irradiation
    • Siddiqui, I.R.; Singh, P.K.; Singh, J.; Singh, J. Three-component solvent-free diastereoselective formation of oxo-thiazolidinylthiazoles under microwave irradiation. J. Chem. Res. 2004, 8, 554-555.
    • (2004) J. Chem. Res , vol.8 , pp. 554-555
    • Siddiqui, I.R.1    Singh, P.K.2    Singh, J.3    Singh, J.4
  • 21
    • 28244447671 scopus 로고    scopus 로고
    • Facile synthesis and fungicidal activity of novel 4,4′-bis[2″-(5‴-substituted rhodanin-3‴-yl)thiazol-4‴-yl]bibenzyls
    • Siddiqui, I.R.; Singh, P.K.; Singh, J.; Singh, J. Facile synthesis and fungicidal activity of novel 4,4′-bis[2″-(5‴-substituted rhodanin-3‴-yl)thiazol-4‴-yl]bibenzyls. Indian J. Chem. 2005,44B, 2102-2106.
    • (2005) Indian J. Chem , vol.44 B , pp. 2102-2106
    • Siddiqui, I.R.1    Singh, P.K.2    Singh, J.3    Singh, J.4
  • 22
    • 28244496516 scopus 로고    scopus 로고
    • Novel clay-catalysed expeditious cyclization to bis-benzothiazepine
    • Siddiqui, I.R.; Singh, P.K.; Srivastava, V.; Singh, J. Novel clay-catalysed expeditious cyclization to bis-benzothiazepine. Indian J. Chem. 2005, 44B, 2178-2182.
    • (2005) Indian J. Chem , vol.44 B , pp. 2178-2182
    • Siddiqui, I.R.1    Singh, P.K.2    Srivastava, V.3    Singh, J.4
  • 23
    • 33749183662 scopus 로고    scopus 로고
    • Environmentally benign synthesis and fungicidal activity of heteryl analogues of bibenzyl
    • Siddiqui, I.R.; Singh, P.K.; Singh, J.; Singh, J.; Environmentally benign synthesis and fungicidal activity of heteryl analogues of bibenzyl. Indian J. Heterocyclic Chem. 2003, 15, 375-378.
    • (2003) Indian J. Heterocyclic Chem , vol.15 , pp. 375-378
    • Siddiqui, I.R.1    Singh, P.K.2    Singh, J.3    Singh, J.4
  • 24
    • 0000784233 scopus 로고    scopus 로고
    • Reactions of allyl phenyl ether in high-temperature water with conventional and microwave heating
    • Bagnell, L.; Cablewski, T.; Strauss, C.R.; Trainor, R.W. Reactions of allyl phenyl ether in high-temperature water with conventional and microwave heating. J. Org. Chem. 1996, 61, 7355-7359.
    • (1996) J. Org. Chem , vol.61 , pp. 7355-7359
    • Bagnell, L.1    Cablewski, T.2    Strauss, C.R.3    Trainor, R.W.4
  • 25
    • 0032582729 scopus 로고    scopus 로고
    • An expeditious and solvent-free synthesis of 2-amino-substituted isoflav-3-enes using microwave irradiation
    • Varma, R.S.; Dahiya, R. An expeditious and solvent-free synthesis of 2-amino-substituted isoflav-3-enes using microwave irradiation. J. Org. Chem. 1998, 63, 8038-8041.
    • (1998) J. Org. Chem , vol.63 , pp. 8038-8041
    • Varma, R.S.1    Dahiya, R.2
  • 27
    • 0006419220 scopus 로고
    • 3-glycosyl-4-hydroxyhexahydropyrimidine-2- thiones and their acyclic glycosylthiourea precursors as stimulators of non-specific resistance to infection
    • Ignatova, L.A.; Shutalev, A.D.; Unkovskii, B.V.; Sinilova, N.G.; Duplishcheva, A.P. N-glycosides. V. 3-glycosyl-4-hydroxyhexahydropyrimidine-2- thiones and their acyclic glycosylthiourea precursors as stimulators of non-specific resistance to infection. Pharmaceutical Chem. J. 1985, 19, 847-852.
    • (1985) Pharmaceutical Chem. J , vol.19 , pp. 847-852
    • Ignatova, L.A.1    Shutalev, A.D.2    Unkovskii, B.V.3    Sinilova, N.G.4    Duplishcheva, A.P.5    N-glycosides, V.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.