메뉴 건너뛰기




Volumn 13, Issue 6, 2011, Pages 659-666

Pseudo-five-component reaction between 3-formylchromones, Meldrum's acid, isocyanides and primary arylamines: Diversity-oriented synthesis of novel chromone-containing peptidomimetics

Author keywords

3 formylchromone; isocyanide; Meldrum's acid; multicomponent reaction; triamide

Indexed keywords

AMIDE; AMINE; AROMATIC HYDROCARBON; CARBON; CHROMONE DERIVATIVE; CYANIDE; DIOXANE DERIVATIVE; FORMYLCHROMONE; MELDRUM ACID; NITROGEN; OXYGEN; PEPTIDOMIMETIC AGENT;

EID: 81255184716     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co200125a     Document Type: Article
Times cited : (35)

References (87)
  • 1
    • 33751034904 scopus 로고    scopus 로고
    • Emerging methods in amide- and peptide-bond formation
    • Bode, J. W. Emerging Methods in Amide- and Peptide-Bond Formation Curr. Opin. Drug Discovery Dev. 2006, 9, 765-775 (Pubitemid 44759567)
    • (2006) Current Opinion in Drug Discovery and Development , vol.9 , Issue.6 , pp. 765-775
    • Bode, J.W.1
  • 2
    • 0007193238 scopus 로고    scopus 로고
    • Chemical synthesis of natural product peptides: Coupling methods for the incorporation of noncoded amino acids into peptides
    • Humphrey, J. M.; Chamberlin, A. R. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides Chem. Rev. 1997, 97, 2243-2266 (Pubitemid 127661210)
    • (1997) Chemical Reviews , vol.97 , Issue.6 , pp. 2243-2266
    • Humphrey, J.M.1    Chamberlin, A.R.2
  • 4
    • 33846822139 scopus 로고    scopus 로고
    • T-scale as a novel vector of topological descriptors for amino acids and its application in QSARs of peptides
    • DOI 10.1016/j.molstruc.2006.07.004, PII S0022286006006314
    • Tian, F.-F.; Zhou, P.; Li, Z.-L. T-scale as A Novel Vector of Topological Descriptors for Amino Acids and Its Application in QSARs of Peptides J. Mol. Struct. 2007, 830, 106-115 (Pubitemid 46216323)
    • (2007) Journal of Molecular Structure , vol.830 , Issue.1-3 , pp. 106-115
    • Tian, F.1    Zhou, P.2    Li, Z.3
  • 5
    • 66149084854 scopus 로고    scopus 로고
    • Structural Parameter Characterization and Bioactivity Simulation Based on Peptide Sequence
    • Shu, M.; Mei, H.; Yang, S.; Liao, L.; Li, Z. Structural Parameter Characterization and Bioactivity Simulation Based on Peptide Sequence QSAR Comb. Sci. 2009, 28, 27-35
    • (2009) QSAR Comb. Sci. , vol.28 , pp. 27-35
    • Shu, M.1    Mei, H.2    Yang, S.3    Liao, L.4    Li, Z.5
  • 6
    • 2442696373 scopus 로고    scopus 로고
    • Bioactivity of a peptide derived from acetylcholinesterase in hippocampal organotypic cultures
    • DOI 10.1007/s00221-003-1757-1
    • Day, T.; Greenfield, S. A. Bioactivity of A Peptide Derived from Acetylcholinesterase in Hippocampal Organohpic Cultures Exp. Brain Res. 2004, 155, 500-508 (Pubitemid 38657161)
    • (2004) Experimental Brain Research , vol.155 , Issue.4 , pp. 500-508
    • Day, T.1    Greenfield, S.A.2
  • 7
    • 0036727255 scopus 로고    scopus 로고
    • Lactobacillus plantarum MiLAB 393 produces the antifungal cyclic dipeptides cyclo(L-Phe-L-Pro) and cyclo(L-Phe-trans-4-OH-L-Pro) and 3-phenyllactic acid
    • DOI 10.1128/AEM.68.9.4322-4327.2002
    • Strom, K.; Sjogren, J.; Broberg, A.; Schnurer, J. Lactobacillus plantarum MiLAB 393 Produces the Antifungal Cyclic Dipeptides Cyclo(l -Phe- l -Pro) and Cyclo(l -Phe- trans -4-OH- l -Pro) and 3-Phenyllactic Acid Appl. Environ. Microbiol. 2002, 68, 4322-4327 (Pubitemid 34988112)
    • (2002) Applied and Environmental Microbiology , vol.68 , Issue.9 , pp. 4322-4327
    • Strom, K.1    Sjogren, J.2    Broberg, A.3    Schnurer, J.4
  • 9
    • 0028834234 scopus 로고
    • Tryprostatins A and B, Novel Mammalian Cell Cycle Inhibitors Produced by Aspergillus fumigatus
    • Cui, C. B.; Kakeya, H.; Okada, G.; Onose, R.; Ubukata, M.; Takahashi, I.; Isono, K.; Osada, H. Tryprostatins A and B, Novel Mammalian Cell Cycle Inhibitors Produced by Aspergillus fumigatus Antibiotics 1995, 48, 1382-1384
    • (1995) Antibiotics , vol.48 , pp. 1382-1384
    • Cui, C.B.1    Kakeya, H.2    Okada, G.3    Onose, R.4    Ubukata, M.5    Takahashi, I.6    Isono, K.7    Osada, H.8
  • 10
    • 0031060189 scopus 로고    scopus 로고
    • Novel mammalian cell cycle inhibitors, cyclotryprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase
    • DOI 10.1016/S0040-4020(96)00978-7, PII S0040402096009787
    • Cui, C. B.; Kakeya, H.; Osada, H. Novel Mammalian Cell Cycle Inhibitors, Cyclotryprostatins A-D, Produced by Aspergillus Fumigatus, Which Inhibit Mammalian Cell Cycle at G2/M Phase Tetrahedron 1997, 53, 59-72 (Pubitemid 26413221)
    • (1997) Tetrahedron , vol.53 , Issue.1 , pp. 59-72
    • Cui, C.-B.1    Kakeya, H.2    Osada, H.3
  • 11
    • 23444442242 scopus 로고    scopus 로고
    • Neuroprotective effects of novel small peptides in vitro and after brain injury
    • DOI 10.1016/j.neuropharm.2005.04.001, PII S0028390805001346
    • Faden, A. I.; Movsesyan, V. A.; Knoblach, S. M.; Ahmed, F.; Cernak, I. Neuroprotective Effects of Novel Small Peptides in vitro and after Brain Injury Neuropharmacology 2005, 49, 410-424 (Pubitemid 41112828)
    • (2005) Neuropharmacology , vol.49 , Issue.3 , pp. 410-424
    • Faden, A.I.1    Movsesyan, V.A.2    Knoblach, S.M.3    Ahmed, F.4    Cernak, I.5
  • 12
    • 0030600506 scopus 로고    scopus 로고
    • Effect of alaptide, its analogues and oxiracetam on memory for an elevated plus-maze in mice
    • DOI 10.1016/S0014-2999(96)00485-2, PII S0014299996004852
    • Hlinak, Z.; Vinsova, J.; Kasafirek, E. Effect of Alaptide, Its Analogues and Oxiracetam on Memory for An Elevated Plus-Maze in Mice Eur. J. Pharmacol. 1996, 314, 1-7 (Pubitemid 26378879)
    • (1996) European Journal of Pharmacology , vol.314 , Issue.1-2 , pp. 1-7
    • Hlinak, Z.1    Vinsova, J.2    Kasafirek, E.3
  • 13
    • 67650954421 scopus 로고    scopus 로고
    • Facile Synthesis of Dipeptidomimetics of p-Aminobenzoic Acid and Their Antidiabetic Activity
    • Tang, X.; Fan, L.; Yu, H.; Liao, Y.; Yang, D. Facile Synthesis of Dipeptidomimetics of p-Aminobenzoic Acid and Their Antidiabetic Activity Chin. J. Org. Chem. 2009, 29, 595-600
    • (2009) Chin. J. Org. Chem. , vol.29 , pp. 595-600
    • Tang, X.1    Fan, L.2    Yu, H.3    Liao, Y.4    Yang, D.5
  • 15
    • 33750496596 scopus 로고    scopus 로고
    • Facile synthesis of non-steroidal anti-inflammatory active bisbenzamide-containing compounds
    • DOI 10.1016/j.bmc.2006.08.032, PII S0968089606006936
    • Girgis, A. S.; Ellithey, M. Facile Synthesis of Non-steroidal Anti-inflammatory Active Bisbenzamide-containing Compounds Bioorg. Med. Chem. 2006, 14, 8527-8532 (Pubitemid 44667531)
    • (2006) Bioorganic and Medicinal Chemistry , vol.14 , Issue.24 , pp. 8527-8532
    • Girgis, A.S.1    Ellithey, M.2
  • 16
    • 0036924734 scopus 로고    scopus 로고
    • Phenolic Compounds of Plants of the Scutellaria. Distribution, Structure and Properties
    • Malikov, V. M.; Yuldashev, M. P. Phenolic Compounds of Plants of the Scutellaria. Distribution, Structure and Properties Chem. Nat. Compd. 2002, 38, 358-406
    • (2002) Chem. Nat. Compd. , vol.38 , pp. 358-406
    • Malikov, V.M.1    Yuldashev, M.P.2
  • 17
    • 0033973978 scopus 로고    scopus 로고
    • Isolation and characterization of methoxylated flavones in the flowers of Primula veris by liquid chromatography and mass spectrometry
    • DOI 10.1016/S0021-9673(99)00950-4, PII S0021967399009504
    • Huck, C. W.; Huber, C. G.; Ongania, K.-H.; Bonn, G. K. Isolation and Characterization of Methoxylated Flavones from the Flowers of Primula Veris by Liquid Chromatography and Mass Spectrometry Chromatogr. A 2000, 870, 453-462 (Pubitemid 30077449)
    • (2000) Journal of Chromatography A , vol.870 , Issue.1-2 , pp. 453-462
    • Huck, C.W.1    Huber, C.G.2    Ongania, K.-H.3    Bonn, G.K.4
  • 18
    • 0036637111 scopus 로고    scopus 로고
    • Antiproliferative constituents in plants 10. Flavones from the leaves of Lantana montevidensis Briq. and consideration of structure-activity relationship
    • DOI 10.1248/bpb.25.875
    • Nagao, T.; Abe, F.; Kinjo, J.; Okabe, H. Antiproliferative Constituents in Plants. 10. Flavones from the Leaves of Lantana Montevidensis BRIQ. and Consideration of Structure-Activity Relationship Biol. Pharm. Bull. 2002, 25, 875-879 (Pubitemid 40022116)
    • (2002) Biological and Pharmaceutical Bulletin , vol.25 , Issue.7 , pp. 875-879
    • Nagao, T.1    Abe, F.2    Kinjo, J.3    Okabe, H.4
  • 19
    • 0035543633 scopus 로고    scopus 로고
    • Plant natural products with leishmanicidal activity
    • DOI 10.1039/b100455g
    • Chan-Bacab, M. J.; Peña-Rodríguez, L. M. Plant Natural Products with Leishmanicidal Activity Nat. Prod. Rep. 2001, 18, 674-688 (Pubitemid 34010018)
    • (2001) Natural Product Reports , vol.18 , Issue.6 , pp. 674-688
    • Chan-Bacab, M.J.1    Pena-Rodriguez, L.M.2
  • 20
    • 0033180428 scopus 로고    scopus 로고
    • Recent advances in chemical ecology
    • DOI 10.1039/a804621b
    • Harborne, J. B. Recent Advances in Chemical Ecology Nat. Prod. Rep. 1999, 16, 509-523 (Pubitemid 29395700)
    • (1999) Natural Product Reports , vol.16 , Issue.4 , pp. 509-523
    • Harborne, J.B.1
  • 22
    • 0033774027 scopus 로고    scopus 로고
    • Inhibitory Activity of Flavonoids and Tannins Against HIV-1 Protease
    • Xu, H.-X.; Wan, M.; Dong, H.; But, P. P.-H.; Foo, L. Y. Inhibitory Activity of Flavonoids and Tannins Against HIV-1 Protease Biol. Pharm. Bull. 2000, 23, 1072-1076
    • (2000) Biol. Pharm. Bull. , vol.23 , pp. 1072-1076
    • Xu, H.-X.1    Wan, M.2    Dong, H.3    But, P.P.-H.4    Foo, L.Y.5
  • 23
    • 0037687736 scopus 로고    scopus 로고
    • Anti-AIDS agents 54. A potent anti-HIV chalcone and flavonoids from genus Desmos
    • DOI 10.1016/S0960-894X(03)00197-5
    • Wu, J.-H.; Wang, X.-H.; Yi, Y.-H.; Lee, K.-H. Anti-AIDS Agents 54. A Potent Anti-HIV Chalcone and Flavonoids from Genus Desmos Bioorg. Med. Chem. Lett. 2003, 13, 1813-1815 (Pubitemid 36561171)
    • (2003) Bioorganic and Medicinal Chemistry Letters , vol.13 , Issue.10 , pp. 1813-1815
    • Wu, J.-H.1    Wang, X.-H.2    Yi, Y.-H.3    Lee, K.-H.4
  • 25
    • 0343618665 scopus 로고    scopus 로고
    • Antiviral effect of flavonoids on the dengue virus
    • DOI 10.1002/(SICI)1099-1573(200003)14:2<89::AID-PTR569>3.0.CO;2-C
    • Sánchez, I.; Gómez-Garibay, F.; Taboada, J.; Ruiz, B. H. Antiviral Effect of Flavonoids on the Dengue Virus Phytother. Res. 2000, 14, 89-92 (Pubitemid 30168556)
    • (2000) Phytotherapy Research , vol.14 , Issue.2 , pp. 89-92
    • Sanchez, I.1    Gomez-Garibay, F.2    Taboada, J.3    Ruiz, B.H.4
  • 26
    • 0033774579 scopus 로고    scopus 로고
    • In Vitro Inhibitory Effect of Some Flavonoids on Rotavirus Infectivity
    • Bae, E.-A.; Han, M. J.; Lee, M.; Kim, D.-H. In Vitro Inhibitory Effect of Some Flavonoids on Rotavirus Infectivity Biol. Pharm. Bull. 2000, 23, 1122-1124
    • (2000) Biol. Pharm. Bull. , vol.23 , pp. 1122-1124
    • Bae, E.-A.1    Han, M.J.2    Lee, M.3    Kim, D.-H.4
  • 28
    • 0032753836 scopus 로고    scopus 로고
    • Reactivities of flavonoids with different hydroxyl substituents for the cleavage of DNA in the presence of Cu(II)
    • DOI 10.1002/(SICI)1099-1573(199911)13:7<609::AID-PTR566>3.0.CO;2-I
    • Jain, A.; Martin, M. C.; Parveen, N.; Khan, N. U.; Parish, J. H.; Hadi, S. M. Reactivities of Flavonoids with Different Hydroxyl Substituents for the Cleavage of DNA in the Presence of Cu(II) Phytother. Res. 1999, 13, 609-612 (Pubitemid 29520940)
    • (1999) Phytotherapy Research , vol.13 , Issue.7 , pp. 609-612
    • Jain, A.1    Martin, M.C.2    Parveen, N.3    Khan, N.U.4    Parish, J.H.5    Hadi, S.M.6
  • 29
    • 85008306863 scopus 로고
    • Antimutagenic Activity of Water Extracts of Black Tea and Oolong Tea
    • Yamada, J.; Tomita, Y. Antimutagenic Activity of Water Extracts of Black Tea and Oolong Tea Biosci., Biotech., Biochem. 1994, 58, 2197-2200
    • (1994) Biosci., Biotech., Biochem. , vol.58 , pp. 2197-2200
    • Yamada, J.1    Tomita, Y.2
  • 30
    • 0036519363 scopus 로고    scopus 로고
    • DNA and its associated processes as targets for cancer therapy
    • Hurley, L. H. DNA and Its Associated Process as Targets for Cancer Therapy Nat. Rev. Cancer 2002, 2, 188-200 (Pubitemid 37328788)
    • (2002) Nature Reviews Cancer , vol.2 , Issue.3 , pp. 188-200
    • Hurley, L.H.1
  • 31
    • 0035206465 scopus 로고    scopus 로고
    • Secondary DNA structures as molecular targets for cancer therapeutics
    • DOI 10.1042/0300-5127:0290692
    • Hurley, L. H. Secondary DNA Structures as Molecular Targets for Cancer Therapeutics Biochem. Soc. Trans. 2001, 29, 692-696 (Pubitemid 33131762)
    • (2001) Biochemical Society Transactions , vol.29 , Issue.6 , pp. 692-696
    • Hurley, L.H.1
  • 32
    • 0019303385 scopus 로고
    • Psorospermin, a new antileukemic xanthone from Psorospermum febrifugum
    • DOI 10.1021/np50008a010
    • Kupchan, S. M.; Streelmann, D. R.; Sneden, A. T. Psorospermin, A New Antileukemic Xanthone from Psorospermum febrifugum J. Nat. Prod. 1980, 43, 296-301 (Pubitemid 10020148)
    • (1980) Journal of Natural Products , vol.43 , Issue.2 , pp. 296-301
    • Kupchan, S.M.1    Streelman, D.R.2    Sneden, A.T.3
  • 33
    • 0000167527 scopus 로고    scopus 로고
    • Pluramycins. Old Drugs Having Modern Friends in Structural Biology
    • Hansen, M. R.; Hurley, L. H. Pluramycins. Old Drugs Having Modern Friends in Structural Biology Acc. Chem. Res. 1996, 29, 249-258
    • (1996) Acc. Chem. Res. , vol.29 , pp. 249-258
    • Hansen, M.R.1    Hurley, L.H.2
  • 35
    • 0034831086 scopus 로고    scopus 로고
    • Advances in cancer therapy with plant based natural products
    • Mukherjee, A. K.; Basu, S.; Sarkar, N.; Ghosh, A. C. Advances in Cancer Therapy with Plant Based Natural Products Curr. Med. Chem. 2001, 8, 1467-1486 (Pubitemid 32894010)
    • (2001) Current Medicinal Chemistry , vol.8 , Issue.12 , pp. 1467-1486
    • Mukherjee, A.K.1    Basu, S.2    Sarkar, N.3    Ghosh, A.C.4
  • 37
    • 77956763614 scopus 로고    scopus 로고
    • Antioxidant and Chelating Properties of Flavonoids. In: Antioxidants in Disease Mechanisms and Therapy
    • In; Sies, H. Academic: San Diego, CA, Vol.
    • Korkina, G. L.; Afanas'ev, I. B. Antioxidant and Chelating Properties of Flavonoids. In: Antioxidants in Disease Mechanisms and Therapy. In Advances in Pharmacology; Sies, H., Ed.; Academic: San Diego, CA, 1997; Vol. 38, pp 151-163
    • (1997) Advances in Pharmacology , vol.38 , pp. 151-163
    • Korkina, G.L.1    Afanas'Ev, I.B.2
  • 39
    • 0038460855 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of psorospermin/quinobenzoxazine hybrids as structurally novel antitumor agents
    • DOI 10.1021/jm030096i
    • Kim, M. Y.; Na, Y.; Vankayalapati, H.; Gleason-Guzman, M.; Hurley, L. H. Design, Synthesis, and Evaluation of Psorospermin/Quinobenzoxazine Hybrids as Structurally Novel Antitumor Agents J. Med. Chem. 2003, 46, 2958-2972 (Pubitemid 36775920)
    • (2003) Journal of Medicinal Chemistry , vol.46 , Issue.14 , pp. 2958-2972
    • Kim, M.-Y.1    Na, Y.2    Vankayalapati, H.3    Gleason-Guzman, M.4    Hurley, L.H.5
  • 40
    • 14844347928 scopus 로고    scopus 로고
    • Bacterial topoisomerase inhibitors: Quinolone and pyridone antibacterial agents
    • DOI 10.1021/cr030101q
    • Mitscher, L. A. Bacterial Topoisomerase Inhibitors: Quinolone and Pyridone Antibacterial Agents Chem. Rev. 2005, 105, 559-592 (Pubitemid 40351634)
    • (2005) Chemical Reviews , vol.105 , Issue.2 , pp. 559-592
    • Mitscher, L.A.1
  • 41
    • 0025312054 scopus 로고
    • Natural products as a source of potential cancer chemotherapeutic and chemopreventive agents
    • DOI 10.1021/np50067a003
    • Cassady, J. M.; Baird, W. M.; Chang, C. J. Natural Products as A Source of Potential Cancer Chemotherapeutic and Chemopreventive Agents J. Nat. Prod. 1990, 53, 23-41 (Pubitemid 20152034)
    • (1990) Journal of Natural Products (Lloydia) , vol.53 , Issue.1 , pp. 23-41
    • Cassady, J.M.1    Baird, W.M.2    Chang, C.-J.3
  • 42
    • 0019303385 scopus 로고
    • Psorospermin, a new antileukemic xanthone from Psorospermum febrifugum
    • DOI 10.1021/np50008a010
    • Kupchan, S. M.; Streelman, D. R.; Sneden, A. T. Psorospermin, A New Antileukemic Xanthone from Psorospermum febrifugum J. Nat. Prod. 1980, 43, 296-301 (Pubitemid 10020148)
    • (1980) Journal of Natural Products , vol.43 , Issue.2 , pp. 296-301
    • Kupchan, S.M.1    Streelman, D.R.2    Sneden, A.T.3
  • 47
    • 0029151095 scopus 로고
    • Coniochaetones A and B: New Antifungal Benzopyranones from the Coprophilous Fungus Coniochaeta saccardoi
    • Wang, H.-J.; Gloer, J. B.; Scott, J. A.; Malloch, D. Coniochaetones A and B: New Antifungal Benzopyranones from the Coprophilous Fungus Coniochaeta saccardoi Tetrahedron Lett. 1995, 36, 5847-5850
    • (1995) Tetrahedron Lett. , vol.36 , pp. 5847-5850
    • Wang, H.-J.1    Gloer, J.B.2    Scott, J.A.3    Malloch, D.4
  • 50
    • 31444457188 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of novel 6-chloro-/fluorochromone derivatives as potential topoisomerase inhibitor anticancer agents
    • DOI 10.1016/j.bmcl.2005.11.044, PII S0960894X0501485X
    • Ishar, M. P. S.; Singh, G.; Singh, S.; Sreenivasan, K. K.; Singh, G. Design, Synthesis, and Evaluation of Novel 6-Chloro-/fluorochromone Derivatives as Potential Topoisomerase Inhibitor Anticancer Agents Bioorg. Med. Chem. Lett. 2006, 16, 1366-1370 (Pubitemid 43153730)
    • (2006) Bioorganic and Medicinal Chemistry Letters , vol.16 , Issue.5 , pp. 1366-1370
    • Ishar, M.P.S.1    Singh, G.2    Singh, S.3    Sreenivasan, K.K.4    Singh, G.5
  • 55
    • 62449152302 scopus 로고    scopus 로고
    • Amide Bond Formation: Beyond the Myth of Coupling Reagents
    • Valeur, E.; Bradley, M. Amide Bond Formation: Beyond the Myth of Coupling Reagents Chem. Soc. Rev. 2009, 38, 606-631
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 606-631
    • Valeur, E.1    Bradley, M.2
  • 56
    • 1342302805 scopus 로고    scopus 로고
    • Recent Development of Peptide Coupling Reagents in Organic Synthesis
    • Han, S. Y.; Kim, Y. A. Recent Development of Peptide Coupling Reagents in Organic Synthesis Tetrahedron 2004, 60, 2447-2467
    • (2004) Tetrahedron , vol.60 , pp. 2447-2467
    • Han, S.Y.1    Kim, Y.A.2
  • 57
    • 26844576835 scopus 로고    scopus 로고
    • Amide bond formation and peptide coupling
    • DOI 10.1016/j.tet.2005.08.031, PII S0040402005013876
    • Montalbetti, C. A. G. N.; Falque, V. Amide Bond Formation and Peptide Coupling Tetrahedron 2005, 61, 10827-10852 (Pubitemid 41447509)
    • (2005) Tetrahedron , vol.61 , Issue.46 , pp. 10827-10852
    • Montalbetti, C.A.G.N.1    Falque, V.2
  • 58
    • 0029905917 scopus 로고    scopus 로고
    • Rapid combinatorial synthesis of aminoglycoside antibiotic mimetics: Use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA Rev responsive element
    • DOI 10.1021/ja9612817, PII S0002786396012814
    • Park, W. K. C.; Auer, M.; Jaksche, H.; Wong, C. H. Rapid Combinatorial Synthesis of Aminoglycoside Antibiotics Mimetics: Use of A Polyethylene Glycol-Linked Amine and Neamine Derived Aldehyde in Multicomponent Condensation as A Strategy for the Discovery of New Inhibitors of the HIV RNA Rev Response Element J. Am. Chem. Soc. 1996, 118, 10150-10155 (Pubitemid 26375200)
    • (1996) Journal of the American Chemical Society , vol.118 , Issue.42 , pp. 10150-10155
    • Park, W.K.C.1    Auer, M.2    Jaksche, H.3    Wong, C.-H.4
  • 59
    • 0033554026 scopus 로고    scopus 로고
    • Total Synthesis of Motuporin (Nodularin-V)
    • Bauer, S. M.; Armstrong, R. W. Total Synthesis of Motuporin (Nodularin-V) J. Am. Chem. Soc. 1999, 121, 6355-6366
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6355-6366
    • Bauer, S.M.1    Armstrong, R.W.2
  • 60
    • 0037423987 scopus 로고    scopus 로고
    • Via Ugi reactions to conformationally fixed cyclic peptides
    • Hebach, C.; Kazmaier, U. Via Ugi-Reaction to Conformational Fixed Cyclic Peptides Chem. Commun. 2003, 596-597 (Pubitemid 36337529)
    • (2003) Chemical Communications , Issue.5 , pp. 596-597
    • Hebach, C.1    Kazmaier, U.2
  • 61
    • 23044477815 scopus 로고    scopus 로고
    • Diversity oriented one-pot synthesis of complex macrocycles: Very large steroid-peptoid hybrids from multiple multicomponent reactions including bifunctional building blocks
    • DOI 10.1002/anie.200500019
    • Wessjohann, L. A.; Voigt, B.; Rivera, D. G. Diversity Oriented One-Pot Synthesis of Complex Macrocycles: Very Large Steroid-Peptoid Hybrids from Multiple Multicomponent Reactions Including Bifunctional Building Blocks Angew. Chem., Int. Ed. 2005, 44, 4785-4790 (Pubitemid 41059187)
    • (2005) Angewandte Chemie - International Edition , vol.44 , Issue.30 , pp. 4785-4790
    • Wessjohann, L.A.1    Voigt, B.2    Rivera, D.G.3
  • 62
    • 29144448797 scopus 로고    scopus 로고
    • Phenol Ugi-Smiles systems: Strategies for the multicomponent N-arylation of primary amines with isocyanides, aldehydes, and phenols
    • DOI 10.1002/anie.200502636
    • El Kaïm, L.; Grimaud, L.; Oble, J. Phenol Ugi-Smiles Systems: Strategies for the Multicomponent N-Arylation of Primary Amines with Isocyanides, Aldehydes, and Phenols Angew. Chem., Int. Ed. 2005, 44, 7961-7964 (Pubitemid 41811719)
    • (2005) Angewandte Chemie - International Edition , vol.44 , Issue.48 , pp. 7961-7964
    • El Kaim, L.1    Grimaud, L.2    Oble, J.3
  • 63
    • 33746321616 scopus 로고    scopus 로고
    • Split the Primary Amine in Two: Secondary Diamines May Play the Role of the Primary Amine in the Ugi 4CR
    • Giovenzana, G. B.; Tron, G. C.; Di Paola, S.; Menegotto, I. G.; Pirali, T. Split the Primary Amine in Two: Secondary Diamines May Play the Role of the Primary Amine in the Ugi 4CR Angew. Chem., Int. Ed. 2006, 45, 1099-1102
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 1099-1102
    • Giovenzana, G.B.1    Tron, G.C.2    Di Paola, S.3    Menegotto, I.G.4    Pirali, T.5
  • 64
    • 0036603766 scopus 로고    scopus 로고
    • Recent advances in isocyanide-based multicomponent chemistry
    • DOI 10.1016/S1367-5931(02)00328-9
    • Dömling, A. Recent Advances in Isocyanide-Based Multicomponent Chemistry Curr. Opin. Chem. Biol. 2002, 6, 306-313 (Pubitemid 34522055)
    • (2002) Current Opinion in Chemical Biology , vol.6 , Issue.3 , pp. 306-313
    • Domling, A.1
  • 65
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • DOI 10.1021/cr0505728
    • Dömling, A. Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry Chem. Rev. 2006, 106, 17-89 (Pubitemid 43159621)
    • (2006) Chemical Reviews , vol.106 , Issue.1 , pp. 17-89
    • Domling, A.1
  • 66
    • 34547403674 scopus 로고    scopus 로고
    • IBX-mediated oxidative Ugi-type multicomponent reactions: Application to the N and C1 functionalization of tetrahydroisoquinoline
    • DOI 10.1002/anie.200701603
    • Ngouansavanh, T.; Zhu, J. IBX-Mediated Oxidative Ugi-Type Reaction: Application to the N- and C1-functionalization of Tetrahydroisoquinoline Angew. Chem., Int. Ed. 2007, 46, 5775-5778 (Pubitemid 47172210)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.30 , pp. 5775-5778
    • Ngouansavanh, T.1    Zhu, J.2
  • 67
    • 49049084624 scopus 로고    scopus 로고
    • Simple Synthesis of 7 H -Phenaleno[1,2- b ]furan-7-one Derivatives by One-Pot, Three-Component Reactions
    • Teimouri, M. B.; Mansouri, F. Simple Synthesis of 7 H -Phenaleno[1,2- b ]furan-7-one Derivatives by One-Pot, Three-Component Reactions J. Comb. Chem. 2008, 10, 507-510
    • (2008) J. Comb. Chem. , vol.10 , pp. 507-510
    • Teimouri, M.B.1    Mansouri, F.2
  • 68
    • 33746703318 scopus 로고    scopus 로고
    • Shaken not stirred: A facile synthesis of 1,4-bis(furo[2,3-d]-pyrimidine- 2,4(1H,3H)-dione-5-yl)benzenes by one-pot reaction of isocyanides, N,N'-dimethylbarbituric acid, and terephthaldialdehyde
    • DOI 10.1016/j.bmcl.2006.04.065, PII S0960894X06004963
    • Teimouri, M. B.; Bazhrang, R. Shaken Not Stirred: A Facile Synthesis of 1,4-Bis(furo[2,3-d]pyrimidine-2,4(1H,3H)-dione-5-yl)benzenes by One-Pot Reaction of Isocyanides, N,N′-Dimethylbarbituric Acid and Terephthaldialdehyde Bioorg. Med. Chem. Lett. 2006, 16, 3697-3701 (Pubitemid 44164270)
    • (2006) Bioorganic and Medicinal Chemistry Letters , vol.16 , Issue.14 , pp. 3697-3701
    • Teimouri, M.B.1    Bazhrang, R.2
  • 69
    • 14944360625 scopus 로고    scopus 로고
    • Microwave-assisted three-component condensation on montmorillonite K10: Solvent-free synthesis of furopyrimidines, furocoumarins, and furopyranones
    • DOI 10.1081/SCC-200049779
    • Shaabani, A.; Teimouri, M. B.; Samadi, S.; Soleimani, K. Microwave-Assisted Three-Component Condensation Reactions on Montmorillonite K10: Solvent-Free Synthesis of Furopyrimidines, Furocoumarines and Furopyranones Synth. Commun. 2005, 35, 535-541 (Pubitemid 40365964)
    • (2005) Synthetic Communications , vol.35 , Issue.4 , pp. 535-541
    • Shaabani, A.1    Teimouri, M.B.2    Samadi, S.3    Soleimani, K.4
  • 70
    • 1842633882 scopus 로고    scopus 로고
    • A Novel Three-Component Tetrahydrobenzofurans Synthesis
    • Shaabani, A.; Teimouri, M. B.; Bijanzadeh, H. R. A Novel Three-Component Tetrahydrobenzofurans Synthesis Monatsh. Chem. 2004, 135, 441-446
    • (2004) Monatsh. Chem. , vol.135 , pp. 441-446
    • Shaabani, A.1    Teimouri, M.B.2    Bijanzadeh, H.R.3
  • 71
    • 2442455330 scopus 로고    scopus 로고
    • One-pot three-component condensation reactions in water. An efficient and improved procedure for the synthesis of furan annulated heterocycles
    • DOI 10.1007/s00706-003-0126-x
    • Shaabani, A.; Teimouri, M. B.; Bijanzadeh, H. R. One-Pot Three-Component Condensation Reactions in Water: An Efficient and Improved Procedure for the Synthesis of Furan Annulated Heterocycles Monatsh. Chem. 2004, 135, 589-593 (Pubitemid 38648612)
    • (2004) Monatshefte fur Chemie , vol.135 , Issue.5 , pp. 589-593
    • Shaabani, A.1    Teimouri, M.B.2    Bijanzadeh, H.R.3
  • 72
    • 0347762544 scopus 로고    scopus 로고
    • Introducing a novel class of four-component reactions
    • DOI 10.1023/B:MODI.0000006759.20910.f1
    • Shaabani, A.; Teimouri, M. B.; Bazgir, A.; Bijanzadeh, H. R. Introducing A Novel Class of Four-Component Reactions Mol. Diversity 2003, 6, 199-206 (Pubitemid 38089856)
    • (2003) Molecular Diversity , vol.6 , Issue.3-4 , pp. 199-206
    • Shaabani, A.1    Teimouri, M.B.2    Bazgir, A.3    Bijanzadeh, H.R.4
  • 73
    • 0037049217 scopus 로고    scopus 로고
    • One-pot three component condensation reaction in water: An efficient and improved procedure for the synthesis of furo[2,3-d]pyrimidine-2,4(1H,3H)-diones
    • DOI 10.1016/S0040-4039(02)02260-8, PII S0040403902022608
    • Shaabani, A.; Teimouri, M. B.; Bijanzadeh, H. R. One-Pot Three Component Condensation Reaction in Water: An Efficient and Improved Procedure for the Synthesis of Furo[2,3-d]pyrimidine-2,4(1H,3H)-diones Tetrahedron Lett. 2002, 43, 9151-9154 (Pubitemid 35305089)
    • (2002) Tetrahedron Letters , vol.43 , Issue.50 , pp. 9151-9154
    • Shaabani, A.1    Teimouri, M.B.2    Bijanzadeh, H.R.3
  • 74
    • 76749165827 scopus 로고    scopus 로고
    • Cellulose Sulphuric Acid as A Biodegradable and Reusable Catalyst for the Knoevenagel Condensation
    • Shelke, K. F.; Sapkal, S. B.; Niralwad, K. S.; Shingate, B. B.; Shingare, M. S. Cellulose Sulphuric Acid as A Biodegradable and Reusable Catalyst for the Knoevenagel Condensation Cent. Eur. J. Chem. 2010, 8, 12-18
    • (2010) Cent. Eur. J. Chem. , vol.8 , pp. 12-18
    • Shelke, K.F.1    Sapkal, S.B.2    Niralwad, K.S.3    Shingate, B.B.4    Shingare, M.S.5
  • 75
    • 56049119881 scopus 로고    scopus 로고
    • Synthesis of 3-Hydroxy-2 H -iminolactones and 3-Hydroxy-2 H -pyrrol-2-ones from Reaction between Isocyanides and Methyl 2-Acetylacetoacetate
    • Hazeri, N.; Maghsoodlou, M. T.; Habibi-Khorassani, S. M.; Marandi, G. Synthesis of 3-Hydroxy-2 H -iminolactones and 3-Hydroxy-2 H -pyrrol-2-ones from Reaction between Isocyanides and Methyl 2-Acetylacetoacetate ARKIVOC 2008, xiv, 282-288
    • (2008) ARKIVOC , vol.14 , pp. 282-288
    • Hazeri, N.1    Maghsoodlou, M.T.2    Habibi-Khorassani, S.M.3    Marandi, G.4
  • 76
    • 33847061275 scopus 로고    scopus 로고
    • Expeditious synthesis of imidazo[1,2-c]pyrimidines via a [4+1]-cycloaddition
    • DOI 10.1016/j.tetlet.2007.01.061, PII S0040403907001116
    • Umkehrer, M.; Ross, G.; Jäger, N.; Burdack, C.; Kolb, J.; Hu, H.; Alvim-Gaston, M.; Hulme, C. Expeditious Synthesis of Imidazo[1,2- c ]pyrimidines via A [4 + 1]-Cycloaddition Tetrahedron Lett. 2007, 48, 2213-2216 (Pubitemid 46275844)
    • (2007) Tetrahedron Letters , vol.48 , Issue.12 , pp. 2213-2216
    • Umkehrer, M.1    Ross, G.2    Jager, N.3    Burdack, C.4    Kolb, J.5    Hu, H.6    Alvim-Gaston, M.7    Hulme, C.8
  • 77
    • 1942456710 scopus 로고    scopus 로고
    • Trifluoromethyl-substituted hydantoins, versatile building blocks for rational drug design
    • DOI 10.1016/j.tet.2004.03.025, PII S0040402004003837
    • Wehner, V.; Stilz, H.-U.; Osipov, S. N.; Golubev, A. S.; Sieler, J.; Burger, K. Trifluoromethyl-Substituted Hydantoins, Versatile Building Blocks for Rational Drug Design Tetrahedron 2004, 60, 4295-4302 (Pubitemid 38510158)
    • (2004) Tetrahedron , vol.60 , Issue.19 , pp. 4295-4302
    • Wehner, V.1    Stilz, H.-U.2    Osipov, S.N.3    Golubev, A.S.4    Sieler, J.5    Burger, K.6
  • 78
    • 0037247814 scopus 로고    scopus 로고
    • [4 + 1] Cycloaddition reactions of o-thioquinones with isocyanides: Novel syntheses of 2-imino-1,3-oxathioles
    • Nair, V.; Mathew, B.; Vinod, A. U.; Mathen, J. S.; Ros, S.; Menon, R. S.; Varma, R. L.; Srinivas, R. [4 + 1] Cycloaddition Reactions of o-Thioquinones with Isocyanides: Novel Syntheses of 2-Imino-1,3-oxathioles Synthesis 2003, 662-664 (Pubitemid 36403456)
    • (2003) Synthesis , Issue.5 , pp. 662-664
    • Nair, V.1    Mathew, B.2    Vinod, A.U.3    Mathen, J.S.4    Ros, S.5    Menon, R.S.6    Varma, R.L.7    Srinivas, R.8
  • 79
    • 0038541773 scopus 로고    scopus 로고
    • 3-catalyzed [4+1] cycloaddition of α,β- unsaturated carbonyl compounds and isocyanides leading to unsaturated γ-lactone derivatives
    • DOI 10.1021/ja035014u
    • 3-Catalyzed [4 + 1] Cycloaddition of α,β-Unsaturated Carbonyl Compounds and Isocyanides Leading to Unsaturated γ-Lactone Derivatives J. Am. Chem. Soc. 2003, 125, 7812-7813 (Pubitemid 36782153)
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.26 , pp. 7812-7813
    • Chatani, N.1    Oshita, M.2    Tobisu, M.3    Ishii, Y.4    Murai, S.5
  • 80
    • 0020044391 scopus 로고
    • A new approach for stereoselective synthesis of γ-butyrolactones
    • DOI 10.1021/jo00343a030
    • Ito, Y.; Kato, H.; Saegusa, T. A New Approach for Stereoselective Synthesis of γ-Butyrolactones J. Org. Chem. 1982, 47, 741-743 (Pubitemid 12140201)
    • (1982) Journal of Organic Chemistry , vol.47 , Issue.4 , pp. 741-743
    • Ito, Y.1    Kato, H.2    Saegusa, T.3
  • 81
    • 0000145083 scopus 로고
    • Meldrum's Acid in Organic Synthesis. 1. A Convenient One-pot Synthesis of Ethyl Indolepropionates
    • Oikawa, Y.; Hirasawa, H.; Yonemitsu, O. Meldrum's Acid in Organic Synthesis. 1. A Convenient One-pot Synthesis of Ethyl Indolepropionates Tetrahedron Lett. 1978, 19, 1759-1762
    • (1978) Tetrahedron Lett. , vol.19 , pp. 1759-1762
    • Oikawa, Y.1    Hirasawa, H.2    Yonemitsu, O.3
  • 82
    • 0007374717 scopus 로고
    • Meldrum's Acid in Organic Synthesis. 2. A General and Versatile Synthesis of β-Keto Esters
    • Oikawa, Y.; Sugano, K.; Yonemitsu, O. Meldrum's Acid in Organic Synthesis. 2. A General and Versatile Synthesis of β-Keto Esters J. Org. Chem. 1978, 43, 2087-2088
    • (1978) J. Org. Chem. , vol.43 , pp. 2087-2088
    • Oikawa, Y.1    Sugano, K.2    Yonemitsu, O.3
  • 83
    • 78650678759 scopus 로고    scopus 로고
    • Ugi-type Four-component Reaction for a Novel Synthesis of 5-Oxo-perhydrofuro[3,2-b]pyran Carboxylate Derivatives
    • Subba Reddy, B. V.; Majumder, N.; Hara Gopal, A. V.; Chatterjee, D.; Kunwar, A. C. Ugi-type Four-component Reaction for a Novel Synthesis of 5-Oxo-perhydrofuro[3,2-b]pyran Carboxylate Derivatives Tetrahedron Lett. 2010, 51, 6835-6838
    • (2010) Tetrahedron Lett. , vol.51 , pp. 6835-6838
    • Subba Reddy, B.V.1    Majumder, N.2    Hara Gopal, A.V.3    Chatterjee, D.4    Kunwar, A.C.5
  • 84
    • 48849091594 scopus 로고    scopus 로고
    • Novel Isocyanide-Based Four-Component Reaction: A Facile Synthesis of Fully Substituted 3,4-Dihydrocoumarin Derivatives
    • Shaabani, A.; Soleimani, E.; Rezayan, A. H.; Sarvary, A.; Khavasi, H. R. Novel Isocyanide-Based Four-Component Reaction: A Facile Synthesis of Fully Substituted 3,4-Dihydrocoumarin Derivatives Org. Lett. 2008, 10, 2581-2584
    • (2008) Org. Lett. , vol.10 , pp. 2581-2584
    • Shaabani, A.1    Soleimani, E.2    Rezayan, A.H.3    Sarvary, A.4    Khavasi, H.R.5
  • 85
    • 0035843379 scopus 로고    scopus 로고
    • New and Efficient Synthesis of Dialkyl 2-[1- p -nitrophenyl-2- (alkylamino)-2-oxoethyl]malonates
    • Shaabani, A.; Yavari, I.; Teimouri, M. B.; Bazgir, A.; Bijanzadeh, H. R. New and Efficient Synthesis of Dialkyl 2-[1- p -nitrophenyl-2-(alkylamino)-2- oxoethyl]malonates Tetrahedron 2001, 57, 1375-1375
    • (2001) Tetrahedron , vol.57 , pp. 1375-1375
    • Shaabani, A.1    Yavari, I.2    Teimouri, M.B.3    Bazgir, A.4    Bijanzadeh, H.R.5
  • 87
    • 0036760083 scopus 로고    scopus 로고
    • The Reaction of Alkyl Isocyanides and Arylidene Meldrum's acid Derivatives in the Presence of Water: One-pot Synthesis of 4-(alkylamino)-3- (aryl)-4-oxobutanoic Acids
    • Shaabani, A.; Teimouri, M. B. The Reaction of Alkyl Isocyanides and Arylidene Meldrum's acid Derivatives in the Presence of Water: One-pot Synthesis of 4-(alkylamino)-3-(aryl)-4-oxobutanoic Acids J. Chem. Res. (S) 2002, 433-435
    • (2002) J. Chem. Res. (S) , pp. 433-435
    • Shaabani, A.1    Teimouri, M.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.