메뉴 건너뛰기




Volumn 16, Issue 4, 2014, Pages 176-183

One-pot synthesis of coumarin-3-carboxamides containing a triazole ring via an isocyanide-based six-component reaction

Author keywords

click chemistry; coumarin; isocyanide; multicomponent reaction; triazole

Indexed keywords

COUMARIN DERIVATIVE; CYANIDE; TRIAZOLE DERIVATIVE;

EID: 84898644102     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co4001259     Document Type: Article
Times cited : (46)

References (79)
  • 1
    • 33645470355 scopus 로고    scopus 로고
    • Chemistry and Biological Activity of Natural and Synthetic Prenyloxycoumarins
    • Curini, M.; Cravotto, G.; Epifano, F.; Giannone, G. Chemistry and Biological Activity of Natural and Synthetic Prenyloxycoumarins Curr. Med. Chem. 2006, 13, 199-222
    • (2006) Curr. Med. Chem. , vol.13 , pp. 199-222
    • Curini, M.1    Cravotto, G.2    Epifano, F.3    Giannone, G.4
  • 5
    • 77649210704 scopus 로고    scopus 로고
    • Anti-Influenza Drug Discovery: Structure-Activity Relationship and Mechanistic Insight into Novel Angelicin Derivatives
    • Yeh, J.-Y.; Coumar, M. S.; Horng, J.-T.; Shiao, H.-Y.; Lee, H.-L. Anti-Influenza Drug Discovery: Structure-Activity Relationship and Mechanistic Insight into Novel Angelicin Derivatives J. Med. Chem. 2010, 53, 1519-1533
    • (2010) J. Med. Chem. , vol.53 , pp. 1519-1533
    • Yeh, J.-Y.1    Coumar, M.S.2    Horng, J.-T.3    Shiao, H.-Y.4    Lee, H.-L.5
  • 6
    • 77249123906 scopus 로고    scopus 로고
    • Highly Supperssing Wild-Type HIV-1 and Y181C Mutant HIV-1 Strains by 10-Chloromethyl-11-demethyl-12-oxo-calanolide A with Druggable Profile
    • Xue, H.; Lu, X.; Zheng, P.; Liu, L.; Han, C.; Hu, J.; Liu, Z.; Ma, T.; Li, Y.; Wang, L.; Chen, Z.; Liu, G. Highly Supperssing Wild-Type HIV-1 and Y181C Mutant HIV-1 Strains by 10-Chloromethyl-11-demethyl-12-oxo-calanolide A with Druggable Profile J. Med. Chem. 2010, 53, 1397-1401
    • (2010) J. Med. Chem. , vol.53 , pp. 1397-1401
    • Xue, H.1    Lu, X.2    Zheng, P.3    Liu, L.4    Han, C.5    Hu, J.6    Liu, Z.7    Ma, T.8    Li, Y.9    Wang, L.10    Chen, Z.11    Liu, G.12
  • 7
    • 84856221609 scopus 로고    scopus 로고
    • A Review on Coumarins as Acetylcholinesterase Inhibitors for Alzheimer's Disease
    • Anand, P.; Singh, B.; Singh, N. A Review on Coumarins as Acetylcholinesterase Inhibitors for Alzheimer's Disease Bioorg. Med. Chem. 2012, 20, 1175-1180
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 1175-1180
    • Anand, P.1    Singh, B.2    Singh, N.3
  • 9
    • 33646544058 scopus 로고    scopus 로고
    • 6-Acyl-4-aryl/alkyl-5,7-dihydroxycoumarins as Anti-Inflammatory Agents
    • Lin, C.-M.; Huang, S.-T.; Lee, F.-W.; Kuo, H.-S.; Lin, M.-H. 6-Acyl-4-aryl/alkyl-5,7-dihydroxycoumarins as Anti-Inflammatory Agents Bioorg. Med. Chem. 2006, 14, 4402-4409
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 4402-4409
    • Lin, C.-M.1    Huang, S.-T.2    Lee, F.-W.3    Kuo, H.-S.4    Lin, M.-H.5
  • 12
    • 78751701180 scopus 로고    scopus 로고
    • Synthesis and Evaluation of a Class of New Coumarin Triazole Derivatives as Potential Antimicrobial Agents
    • Shi, Y.; Zhou, C. Synthesis and Evaluation of a Class of New Coumarin Triazole Derivatives as Potential Antimicrobial Agents Bioorg. Med. Chem. Lett. 2011, 21, 956-960
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 956-960
    • Shi, Y.1    Zhou, C.2
  • 13
    • 0025041309 scopus 로고
    • Structure-Activity Relationships of Polymethoxyflavones and Other Flavonoids as Inhibitors of Non-enzymic Lipid Peroxidation
    • Mora, A.; Paya, M.; Rios, J. L.; Alcaraz, M. J. Structure-Activity Relationships of Polymethoxyflavones and Other Flavonoids as Inhibitors of Non-enzymic Lipid Peroxidation Biochem. Pharmacol. 1990, 40, 793-797
    • (1990) Biochem. Pharmacol. , vol.40 , pp. 793-797
    • Mora, A.1    Paya, M.2    Rios, J.L.3    Alcaraz, M.J.4
  • 14
    • 38949201273 scopus 로고    scopus 로고
    • Modification of DNA with Octadiynyl Side Chains: Synthesis, Base Pairing, and Formation of Fluorescent Coumarin Dye Conjugates of Four Nucleobases by the Alkyne-Azide "click" Reaction
    • Seela, F.; Sirivolu, V. R.; Chittepu, P. Modification of DNA with Octadiynyl Side Chains: Synthesis, Base Pairing, and Formation of Fluorescent Coumarin Dye Conjugates of Four Nucleobases by the Alkyne-Azide "Click" Reaction Bioconjugate Chem. 2008, 19, 211-224
    • (2008) Bioconjugate Chem. , vol.19 , pp. 211-224
    • Seela, F.1    Sirivolu, V.R.2    Chittepu, P.3
  • 15
    • 33751550874 scopus 로고    scopus 로고
    • Synthesis of Coumarin-Nucleoside Conjugates via Huisgen 1,3-Dipolar Cycloaddition
    • Kosiova, I.; Kovackova, S.; Kois, P. Synthesis of Coumarin-Nucleoside Conjugates via Huisgen 1,3-Dipolar Cycloaddition Tetrahedron 2007, 63, 312-320
    • (2007) Tetrahedron , vol.63 , pp. 312-320
    • Kosiova, I.1    Kovackova, S.2    Kois, P.3
  • 16
    • 37549061836 scopus 로고    scopus 로고
    • Non-enzymatic Covalent Protein Labeling Using a Reactive Tag
    • Nonaka, H.; Tsukiji, S.; Ojida, A.; Hamachi, I. Non-enzymatic Covalent Protein Labeling Using a Reactive Tag J. Am. Chem. Soc. 2007, 129, 15777-15779
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 15777-15779
    • Nonaka, H.1    Tsukiji, S.2    Ojida, A.3    Hamachi, I.4
  • 21
    • 72049095332 scopus 로고    scopus 로고
    • Synthesis and Antimicrobial Activity of 7-(2-Substituted Phenylthiazolidinyl)-benzopyran-2-one Derivatives
    • Ronad, P. M.; Noolvi, M. N.; Sapkal, S.; Dharbhamulla, S.; Maddi, V. S. Synthesis and Antimicrobial Activity of 7-(2-Substituted Phenylthiazolidinyl)- benzopyran-2-one Derivatives Eur. J. Med. Chem. 2010, 45, 85-89
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 85-89
    • Ronad, P.M.1    Noolvi, M.N.2    Sapkal, S.3    Dharbhamulla, S.4    Maddi, V.S.5
  • 22
    • 70449642389 scopus 로고    scopus 로고
    • RETRACTED: 2-Azetidinone Derivatives: Design, Synthesis, in vitro Anti-microbial, Cytotoxic Activities and DNA Cleavage Study
    • Keri, R. S.; Hosamani, K. M.; Shingalapur, R. V.; Reddy, H. R. S. RETRACTED: 2-Azetidinone Derivatives: Design, Synthesis, in vitro Anti-microbial, Cytotoxic Activities and DNA Cleavage Study Eur. J. Med. Chem. 2009, 44, 5123-5130
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 5123-5130
    • Keri, R.S.1    Hosamani, K.M.2    Shingalapur, R.V.3    Reddy, H.R.S.4
  • 23
    • 65349183985 scopus 로고    scopus 로고
    • Synthesis and in vitro Study of Novel Bis-[3-(2-Arylmethylidenimino-1,3- thiazol-4-yl)-4-hydroxy-2 H -chromen-2-one-6-yl]methane and bis-[3-(2- arylidenhydrazo-1,3-thiazol-4-yl)-4-hydroxy-2H-chromen-2-one-6-yl]methane as Potential Antimicrobial Agents
    • Raghu, M.; Nagaraj, A.; Reddy, C. S. Synthesis and in vitro Study of Novel Bis-[3-(2-Arylmethylidenimino-1,3-thiazol-4-yl)-4-hydroxy-2 H -chromen-2-one-6-yl]methane and bis-[3-(2-arylidenhydrazo-1,3-thiazol-4-yl)-4- hydroxy-2H-chromen-2-one-6-yl]methane as Potential Antimicrobial Agents J. Heterocycl. Chem. 2009, 46, 261-267
    • (2009) J. Heterocycl. Chem. , vol.46 , pp. 261-267
    • Raghu, M.1    Nagaraj, A.2    Reddy, C.S.3
  • 28
    • 0028757621 scopus 로고
    • Multicomponent Reactions in Organic Chemistry
    • Ugi, I.; Dömling, A.; Horl, W. Multicomponent Reactions in Organic Chemistry Endeavour 1994, 18, 115-122
    • (1994) Endeavour , vol.18 , pp. 115-122
    • Ugi, I.1    Dömling, A.2    Horl, W.3
  • 29
    • 2542509173 scopus 로고    scopus 로고
    • Multicomponent Reactions with Isocyanides
    • Dömling, A.; Ugi, I. Multicomponent Reactions with Isocyanides Angew. Chem., Int. Ed. 2000, 39, 3168-3210
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3168-3210
    • Dömling, A.1    Ugi, I.2
  • 31
    • 31544434530 scopus 로고    scopus 로고
    • Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry
    • Dömling, A. Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry Chem. Rev. 2006, 106, 17-89
    • (2006) Chem. Rev. , vol.106 , pp. 17-89
    • Dömling, A.1
  • 32
    • 65249100749 scopus 로고    scopus 로고
    • Strategies for Innovation in Multicomponent Reaction Design
    • Ganem, B. Strategies for Innovation in Multicomponent Reaction Design Acc. Chem. Res. 2009, 42, 463-472
    • (2009) Acc. Chem. Res. , vol.42 , pp. 463-472
    • Ganem, B.1
  • 33
    • 70349156384 scopus 로고    scopus 로고
    • Natural Product Synthesis Using Multicomponent Reaction Strategies
    • Toure, B. B.; Hall, D. G. Natural Product Synthesis Using Multicomponent Reaction Strategies Chem. Rev. 2009, 109, 4439-4486
    • (2009) Chem. Rev. , vol.109 , pp. 4439-4486
    • Toure, B.B.1    Hall, D.G.2
  • 34
    • 60749120878 scopus 로고    scopus 로고
    • Applications of Multicomponent Reactions to the Synthesis of Diverse Heterocyclic Scaffolds
    • Sunderhaus, J. D.; Martin, S. F. Applications of Multicomponent Reactions to the Synthesis of Diverse Heterocyclic Scaffolds Chem.-Eur. J. 2009, 15, 1300-1308
    • (2009) Chem.-Eur. J. , vol.15 , pp. 1300-1308
    • Sunderhaus, J.D.1    Martin, S.F.2
  • 36
    • 79953294313 scopus 로고    scopus 로고
    • Recent Progress of Isocyanide-based Multicomponent Reactions in Iran
    • Shaabani, A.; Maleki, A.; Rezayan, A. H.; Sarvary, A. Recent Progress of Isocyanide-based Multicomponent Reactions in Iran Mol. Divers. 2011, 15, 41-68
    • (2011) Mol. Divers. , vol.15 , pp. 41-68
    • Shaabani, A.1    Maleki, A.2    Rezayan, A.H.3    Sarvary, A.4
  • 38
    • 0000719799 scopus 로고
    • Angew. Chem. 1993, 105, 634-635.
    • (1993) Angew. Chem. , vol.105 , pp. 634-635
  • 39
    • 0036603766 scopus 로고    scopus 로고
    • Recent Advances in Isocyanide-Based Multicomponent Chemistry
    • Dömling, A. Recent Advances in Isocyanide-Based Multicomponent Chemistry Curr. Opin.Chem. Biol. 2002, 6, 306-313
    • (2002) Curr. Opin.Chem. Biol. , vol.6 , pp. 306-313
    • Dömling, A.1
  • 40
    • 34547403674 scopus 로고    scopus 로고
    • IBX-Mediated Oxidative Ugi-Type Multicomponent Reactions: Application to the N and C1 Functionalization of Tetrahydroisoquinoline
    • Ngouansavanh, T.; Zhu, J. IBX-Mediated Oxidative Ugi-Type Multicomponent Reactions: Application to the N and C1 Functionalization of Tetrahydroisoquinoline Angew. Chem., Int. Ed. 2007, 46, 5775-5778
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 5775-5778
    • Ngouansavanh, T.1    Zhu, J.2
  • 41
    • 33746321616 scopus 로고    scopus 로고
    • A Mimicry of Primary Amines by Bis-Secondary Diamines as Components in the Ugi Four-Component Reaction
    • Giovenzana, G. B.; Tron, G. C.; Di Paola, S.; Menegotto, I. G.; Pirali, T. A Mimicry of Primary Amines by Bis-Secondary Diamines as Components in the Ugi Four-Component Reaction 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
  • 42
    • 29144448797 scopus 로고    scopus 로고
    • Phenol Ugi-Smiles Systems: Strategies for the Multicomponent N-Arylation of Primary Amines with Isocyanides, Aldehydes, and Phenols
    • El Kaim, 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
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 7961-7964
    • El Kaim, L.1    Grimaud, L.2    Oble, J.3
  • 43
    • 0037423987 scopus 로고    scopus 로고
    • Via Ugi Reactions to Conformationally Fixed Cyclic Peptides
    • Hebach, C.; Kazmaier, U. Via Ugi Reactions to Conformationally Fixed Cyclic Peptides Chem. Commun. 2003, 596-597
    • (2003) Chem. Commun. , pp. 596-597
    • Hebach, C.1    Kazmaier, U.2
  • 45
    • 79959782009 scopus 로고    scopus 로고
    • Design and Synthesis of Bile Acid-Peptide Conjugates Linked via Triazole Moiety
    • Sokolova, N. V.; Latyshev, G. V.; Lukashev, N. V.; Nenajdenko, V. G. Design and Synthesis of Bile Acid-Peptide Conjugates Linked via Triazole Moiety Org. Biomol. Chem. 2011, 9, 4921-4926
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 4921-4926
    • Sokolova, N.V.1    Latyshev, G.V.2    Lukashev, N.V.3    Nenajdenko, V.G.4
  • 48
    • 84858705761 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Bio-hybrid Amphiphiles of Coumarin Derivatives by Ugi-Mannich Triazole Randomization Using Copper Catalyzed Alkyne Azide Click Chemistry
    • Pramitha, P.; Bahulayan, D. Stereoselective Synthesis of Bio-hybrid Amphiphiles of Coumarin Derivatives by Ugi-Mannich Triazole Randomization Using Copper Catalyzed Alkyne Azide Click Chemistry Bioorg. Med. Chem. Lett. 2012, 22, 2598-2603
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 2598-2603
    • Pramitha, P.1    Bahulayan, D.2
  • 49
    • 84871797906 scopus 로고    scopus 로고
    • Preparation and Study of an f,f,f′,f″ Covalently Linked Tetranuclear Hetero-Trimetallic Complex - A Europium, Terbium, Dysprosium Triad
    • Sørensen, T. J.; Tropiano, M.; Blackburn, O. A.; Tilney, J. A.; Kenwright, A. M.; Faulkner, S. Preparation and Study of an f,f,f′,f″ Covalently Linked Tetranuclear Hetero-Trimetallic Complex-a Europium, Terbium, Dysprosium Triad Chem. Commun. 2013, 49, 783-785
    • (2013) Chem. Commun. , vol.49 , pp. 783-785
    • Sørensen, T.J.1    Tropiano, M.2    Blackburn, O.A.3    Tilney, J.A.4    Kenwright, A.M.5    Faulkner, S.6
  • 50
    • 84861186622 scopus 로고    scopus 로고
    • A Simple Protocol for the Synthesis of Triazole-Linked Cyclic Glycopeptidomimetics: A Sequential Ugi-MCR and Azide-Alkyne Cycloaddition Approach
    • Samarasimhareddy, M.; Hemantha, H. P.; Sureshbabu, V. V. A Simple Protocol for the Synthesis of Triazole-Linked Cyclic Glycopeptidomimetics: A Sequential Ugi-MCR and Azide-Alkyne Cycloaddition Approach Tetrahedron Lett. 2012, 53, 3104-3107
    • (2012) Tetrahedron Lett. , vol.53 , pp. 3104-3107
    • Samarasimhareddy, M.1    Hemantha, H.P.2    Sureshbabu, V.V.3
  • 51
    • 84856015469 scopus 로고    scopus 로고
    • A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1 H -1,2,3-Triazole-Modified α -Amino Acid Derivatives and Peptidomimetics
    • Niu, T.-F.; Cai, C.; Yi, L. A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1 H -1,2,3-Triazole-Modified α -Amino Acid Derivatives and Peptidomimetics Helv. Chim. Acta 2012, 95, 87-99
    • (2012) Helv. Chim. Acta , vol.95 , pp. 87-99
    • Niu, T.-F.1    Cai, C.2    Yi, L.3
  • 52
    • 0000096835 scopus 로고    scopus 로고
    • Click Chemistry: Diverse Chemical Function from a Few Good Reactions
    • Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click Chemistry: Diverse Chemical Function from a Few Good Reactions Angew. Chem., Int. Ed. 2001, 40, 2004-2021
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 53
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
    • Tornøe, C. W.; Christensen, C.; Meldal, M. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides J. Org. Chem. 2002, 67, 3057-3064
    • (2002) J. Org. Chem. , vol.67 , pp. 3057-3064
    • Tornøe, C.W.1    Christensen, C.2    Meldal, M.3
  • 54
    • 0037099395 scopus 로고    scopus 로고
    • A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective "ligation" of Azides and Terminal Alkynes
    • Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective "Ligation" of Azides and Terminal Alkynes Angew. Chem., Int. Ed. 2002, 41, 2596-2599
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 55
    • 0028063421 scopus 로고
    • 1,2,3-Triazole-[2,5-Bis-O-(tert-butyldimethylsilyl)-.beta. -D-ribofuranosyl]-3′-spiro-5″-(4″-amino-1″, 2″-oxathiole 2″,2″-dioxide) (TSAO) Analogs: Synthesis and Anti-HIV-1 Activity
    • Alvarez, R.; Velazquez, S.; San-Felix, A.; Aquaro, S.; Clercq, E. D.; Perno, C.-F.; Karlsson, A.; Balzarini, J.; Camarasa, M. J. 1,2,3-Triazole-[2,5- Bis-O-(tert-butyldimethylsilyl)-.beta.-D-ribofuranosyl]-3′-spiro-5″- (4″-amino-1″,2″-oxathiole 2″,2″-dioxide) (TSAO) Analogs: Synthesis and Anti-HIV-1 Activity J. Med. Chem. 1994, 37, 4185-4194
    • (1994) J. Med. Chem. , vol.37 , pp. 4185-4194
    • Alvarez, R.1    Velazquez, S.2    San-Felix, A.3    Aquaro, S.4    Clercq, E.D.5    Perno, C.-F.6    Karlsson, A.7    Balzarini, J.8    Camarasa, M.J.9
  • 57
    • 0348109450 scopus 로고    scopus 로고
    • The Growing Impact of Click Chemistry on Drug Discovery
    • Kolb, H. C.; Sharpless, K. B. The Growing Impact of Click Chemistry on Drug Discovery Drug Discovery Today 2003, 8, 1128-1137
    • (2003) Drug Discovery Today , vol.8 , pp. 1128-1137
    • Kolb, H.C.1    Sharpless, K.B.2
  • 59
    • 37049110636 scopus 로고
    • Studies on v-Triazoles. Part 4. The 4-Methoxybenzyl Group, a Versatile N -protecting Group for the Synthesis of N -unsubstituted v-Triazoles
    • Buckle, D. R.; Rockell, C. J. M. Studies on v-Triazoles. Part 4. The 4-Methoxybenzyl Group, a Versatile N -protecting Group for the Synthesis of N -unsubstituted v-Triazoles J. Chem. Soc., Perkin Trans. 1 1982, 627-630
    • (1982) J. Chem. Soc., Perkin Trans. 1 , pp. 627-630
    • Buckle, D.R.1    Rockell, C.J.M.2
  • 60
    • 0020677250 scopus 로고
    • Studies on v-Triazoles. 7. Antiallergic 9-Oxo-1 H, 9 H -benzopyrano[2,3-d]-v-triazoles
    • Buckle, D. R.; Outred, D. J.; Rockell, C. J. M.; Smith, H.; Spicer, B. A. Studies on v-Triazoles. 7. Antiallergic 9-Oxo-1 H, 9 H -benzopyrano[2,3-d]-v- triazoles J. Med. Chem. 1983, 26, 251-254
    • (1983) J. Med. Chem. , vol.26 , pp. 251-254
    • Buckle, D.R.1    Outred, D.J.2    Rockell, C.J.M.3    Smith, H.4    Spicer, B.A.5
  • 61
    • 0023018014 scopus 로고
    • Studies on 1,2,3-Triazoles. 13. (Piperazinylalkoxy)-[1]benzopyrano[2,3- d ]-1,2,3-triazol-9(1 H)-ones with Combined H1-Antihistamine and Mast Cell Stabilizing Properties
    • Buckle, D. R.; Rockell, C. J. M.; Smith, H.; Spicer, B. A. Studies on 1,2,3-Triazoles. 13. (Piperazinylalkoxy)-[1]benzopyrano[2,3- d ]-1,2,3-triazol-9(1 H)-ones with Combined H1-Antihistamine and Mast Cell Stabilizing Properties J. Med. Chem. 1986, 29, 2262-2267
    • (1986) J. Med. Chem. , vol.29 , pp. 2262-2267
    • Buckle, D.R.1    Rockell, C.J.M.2    Smith, H.3    Spicer, B.A.4
  • 62
    • 77949838793 scopus 로고    scopus 로고
    • Synthesis, Biological Activity, and Molecular Modeling Studies of 1 H -1,2,3-Triazole Derivatives of Carbohydrates as α -Glucosidases Inhibitors
    • Ferreira, S. B.; Sodero, A. C. R.; Cardoso, M. F. C.; Lima, E. S.; Kaiser, C. R.; Silva, F. P.; Ferreira, V. F. Synthesis, Biological Activity, and Molecular Modeling Studies of 1 H -1,2,3-Triazole Derivatives of Carbohydrates as α -Glucosidases Inhibitors J. Med. Chem. 2010, 53, 2364-2375
    • (2010) J. Med. Chem. , vol.53 , pp. 2364-2375
    • Ferreira, S.B.1    Sodero, A.C.R.2    Cardoso, M.F.C.3    Lima, E.S.4    Kaiser, C.R.5    Silva, F.P.6    Ferreira, V.F.7
  • 63
    • 84867548404 scopus 로고    scopus 로고
    • A Chirality Rewriting Cycle Mediated by a Dynamic Cyclen-Calcium Complex
    • Ito, H.; Tsukube, H.; Shinoda, S. A Chirality Rewriting Cycle Mediated by a Dynamic Cyclen-Calcium Complex Chem. Commun. 2012, 48, 10954-10956
    • (2012) Chem. Commun. , vol.48 , pp. 10954-10956
    • Ito, H.1    Tsukube, H.2    Shinoda, S.3
  • 64
    • 67649319499 scopus 로고    scopus 로고
    • 8-Aza-7-Deazaguanine Nucleosides and Oligonucleotides with Octadiynyl Side Chains: Synthesis, Functionalization by the Azide-Alkyne 'Click' Reaction and Nucleobase Specific Fluorescence Quenching of Coumarin Dye Conjugates
    • Seela, F.; Xiong, H.; Leonard, P.; Budow, S. 8-Aza-7-Deazaguanine Nucleosides and Oligonucleotides with Octadiynyl Side Chains: Synthesis, Functionalization by the Azide-Alkyne 'Click' Reaction and Nucleobase Specific Fluorescence Quenching of Coumarin Dye Conjugates Org. Biomol. Chem. 2009, 7, 1374-1387
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 1374-1387
    • Seela, F.1    Xiong, H.2    Leonard, P.3    Budow, S.4
  • 65
    • 26844472243 scopus 로고    scopus 로고
    • Selective Dye-Labeling of Newly Synthesized Proteins in Bacterial Cells
    • Beatty, K. E.; Xie, F.; Wang, Q.; Tirrell, D. A. Selective Dye-Labeling of Newly Synthesized Proteins in Bacterial Cells J. Am. Chem. Soc. 2005, 127, 14150-14151
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 14150-14151
    • Beatty, K.E.1    Xie, F.2    Wang, Q.3    Tirrell, D.A.4
  • 66
    • 33748609388 scopus 로고    scopus 로고
    • Click Chemistry as a Reliable Method for the High-Density Postsynthetic Functionalization of Alkyne-Modified DNA
    • Gierlich, J.; Burley, G. A.; Gramlich, P. M. E.; Hammond, D. H.; Carell, T. Click Chemistry as a Reliable Method for the High-Density Postsynthetic Functionalization of Alkyne-Modified DNA Org. Lett. 2006, 8, 3639-3642
    • (2006) Org. Lett. , vol.8 , pp. 3639-3642
    • Gierlich, J.1    Burley, G.A.2    Gramlich, P.M.E.3    Hammond, D.H.4    Carell, T.5
  • 68
    • 38649104163 scopus 로고    scopus 로고
    • Chemical Surface Reactions by Click Chemistry: Coumarin Dye Modification of 11-Bromoundecyltrichlorosilane Monolayers
    • Haensch, C.; Hoeppener, S.; Schubert, U. S. Chemical Surface Reactions by Click Chemistry: Coumarin Dye Modification of 11-Bromoundecyltrichlorosilane Monolayers Nanotechnology 2008, 19, 035703-035710
    • (2008) Nanotechnology , vol.19 , pp. 035703-035710
    • Haensch, C.1    Hoeppener, S.2    Schubert, U.S.3
  • 69
    • 10044258626 scopus 로고    scopus 로고
    • A Fluorogenic 1,3-Dipolar Cycloaddition Reaction of 3-Azidocoumarins and Acetylenes
    • Sivakumar, K.; Xie, F.; Cash, B. M.; Long, S.; Barnhill, H. N.; Wang, Q. A Fluorogenic 1,3-Dipolar Cycloaddition Reaction of 3-Azidocoumarins and Acetylenes Org. Lett. 2004, 6, 4603-4606
    • (2004) Org. Lett. , vol.6 , pp. 4603-4606
    • Sivakumar, K.1    Xie, F.2    Cash, B.M.3    Long, S.4    Barnhill, H.N.5    Wang, Q.6
  • 71
  • 72
    • 68149141342 scopus 로고    scopus 로고
    • A Novel One-Pot Three-(in Situ Five-)Component Condensation Reaction: An Unexpected Approach for the Synthesis of Tetrahydro-2,4-dioxo-1 H -benzo[ b ][1,5]diazepine-3-yl-2-methylpropanamide Derivatives
    • Shaabani, A.; Rezayan, A. H.; Keshipour, S.; Sarvary, A.; Ng, S. W. A Novel One-Pot Three-(in Situ Five-)Component Condensation Reaction: An Unexpected Approach for the Synthesis of Tetrahydro-2,4-dioxo-1 H -benzo[ b ][1,5]diazepine-3-yl-2-methylpropanamide Derivatives Org. Lett. 2009, 11, 3342-3345
    • (2009) Org. Lett. , vol.11 , pp. 3342-3345
    • Shaabani, A.1    Rezayan, A.H.2    Keshipour, S.3    Sarvary, A.4    Ng, S.W.5
  • 73
    • 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
  • 74
    • 66249101971 scopus 로고    scopus 로고
    • Synthesis of Highly Functionalized Bis(4 H -chromene) and 4 H -Benzo[ g ]chromene Derivatives via an Isocyanide-Based Pseudo-Five-Component Reaction
    • Shaabani, A.; Ghadari, R.; Sarvary, A.; Rezayan, A. H. Synthesis of Highly Functionalized Bis(4 H -chromene) and 4 H -Benzo[ g ]chromene Derivatives via an Isocyanide-Based Pseudo-Five-Component Reaction J. Org. Chem. 2009, 74, 4372-4374
    • (2009) J. Org. Chem. , vol.74 , pp. 4372-4374
    • Shaabani, A.1    Ghadari, R.2    Sarvary, A.3    Rezayan, A.H.4
  • 75
    • 70449396591 scopus 로고    scopus 로고
    • Novel One-Pot Three- and Pseudo-Five-Component Reactions: Synthesis of Functionalized Benzo[ g ]- and Dihydropyrano[2,3- g ]chromene Derivatives
    • Shaabani, A.; Ghadari, R.; Ghasemi, S.; Pedarpour, M.; Rezayan, A. H.; Sarvary, A.; Ng, S. W. Novel One-Pot Three- and Pseudo-Five-Component Reactions: Synthesis of Functionalized Benzo[ g ]- and Dihydropyrano[2,3- g ]chromene Derivatives J. Comb. Chem. 2009, 11, 956-959
    • (2009) J. Comb. Chem. , vol.11 , pp. 956-959
    • Shaabani, A.1    Ghadari, R.2    Ghasemi, S.3    Pedarpour, M.4    Rezayan, A.H.5    Sarvary, A.6    Ng, S.W.7
  • 77
    • 84859012651 scopus 로고    scopus 로고
    • Efficient Synthesis of Novel Coumarin-3-carboxamides (=2-Oxo-2 H -1-benzopyran-3-carboxamides) Containing Lipophilic Spacers
    • Balalaie, S.; Bigdeli, M. A.; Sheikhhosseini, E.; Habibi, A.; Piri Moghadam, H.; Naderi, M. Efficient Synthesis of Novel Coumarin-3-carboxamides (=2-Oxo-2 H -1-benzopyran-3-carboxamides) Containing Lipophilic Spacers Helv. Chim. Acta 2012, 95, 528-535
    • (2012) Helv. Chim. Acta , vol.95 , pp. 528-535
    • Balalaie, S.1    Bigdeli, M.A.2    Sheikhhosseini, E.3    Habibi, A.4    Piri Moghadam, H.5    Naderi, M.6
  • 78
    • 33646441898 scopus 로고    scopus 로고
    • Theoretical Modeling of Interface Specific Vibrational Spectroscopy: Methods and Applications to Aqueous Interfaces
    • Perry, A.; Neipert, C.; Space, B. Theoretical Modeling of Interface Specific Vibrational Spectroscopy: Methods and Applications to Aqueous Interfaces Chem. Rev. 2006, 106, 1234-1258
    • (2006) Chem. Rev. , vol.106 , pp. 1234-1258
    • Perry, A.1    Neipert, C.2    Space, B.3
  • 79
    • 57249113661 scopus 로고    scopus 로고
    • Uncatalysed Reactions in Water: Part 2. Preparation of 3-Carboxycoumarins
    • Maggi, R.; Bigi, F.; Carloni, S.; Mazzacani, A.; Sartori, G. Uncatalysed Reactions in Water: Part 2. Preparation of 3-Carboxycoumarins Green Chem. 2001, 3, 173-174
    • (2001) Green Chem. , vol.3 , pp. 173-174
    • Maggi, R.1    Bigi, F.2    Carloni, S.3    Mazzacani, A.4    Sartori, G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.