메뉴 건너뛰기




Volumn 116, Issue 10, 2016, Pages 5689-5743

Alkaloids and Isoprenoids Modification by Copper(I)-Catalyzed Huisgen 1,3-Dipolar Cycloaddition (Click Chemistry): Toward New Functions and Molecular Architectures

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOIDS; CATALYSIS; DRUG DELIVERY; LIPIDS; SYNTHESIS (CHEMICAL);

EID: 84973468713     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.5b00302     Document Type: Review
Times cited : (228)

References (244)
  • 1
    • 84876002671 scopus 로고    scopus 로고
    • Natural Products: A Continuing Source of Novel Drug Leads
    • Cragg, G. M.; Newman, D. J. Natural Products: a Continuing Source of Novel Drug Leads Biochim. Biophys. Acta, Gen. Subj. 2013, 1830, 3670-3695 10.1016/j.bbagen.2013.02.008
    • (2013) Biochim. Biophys. Acta, Gen. Subj. , vol.1830 , pp. 3670-3695
    • Cragg, G.M.1    Newman, D.J.2
  • 2
    • 84858308226 scopus 로고    scopus 로고
    • Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
    • Newman, D. J.; Cragg, G. M. Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010 J. Nat. Prod. 2012, 75, 311-335 10.1021/np200906s
    • (2012) J. Nat. Prod. , vol.75 , pp. 311-335
    • Newman, D.J.1    Cragg, G.M.2
  • 3
    • 80053203292 scopus 로고    scopus 로고
    • Natural Products: An Evolving Role in Future Drug Discovery
    • Mishra, B. B.; Tiwari, V. K. Natural Products: an Evolving Role in Future Drug Discovery Eur. J. Med. Chem. 2011, 46, 4769-4807 10.1016/j.ejmech.2011.07.057
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 4769-4807
    • Mishra, B.B.1    Tiwari, V.K.2
  • 4
    • 84897443754 scopus 로고    scopus 로고
    • New Horizons for Old Drugs and Drug Leads
    • Cragg, G. M.; Grothaus, P. G.; Newman, D. J. New Horizons for Old Drugs and Drug Leads J. Nat. Prod. 2014, 77, 703-723 10.1021/np5000796
    • (2014) J. Nat. Prod. , vol.77 , pp. 703-723
    • Cragg, G.M.1    Grothaus, P.G.2    Newman, D.J.3
  • 5
    • 0032491014 scopus 로고    scopus 로고
    • Natural Products Analogs as Scaffolds for Supramolecular and Combinatorial Chemistry
    • Mink, D.; Mecozzi, S.; Rebek, J., Jr. Natural Products Analogs as Scaffolds for Supramolecular and Combinatorial Chemistry Tetrahedron Lett. 1998, 39, 5709-5712 10.1016/S0040-4039(98)01170-8
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5709-5712
    • Mink, D.1    Mecozzi, S.2    Rebek, J.3
  • 7
    • 52449100159 scopus 로고    scopus 로고
    • Natural Products as Inspiration for the Development of Asymmetric Catalysis
    • Mohr, J. T.; Krout, M. R.; Stoltz, B. M. Natural Products as Inspiration for the Development of Asymmetric Catalysis Nature 2008, 455, 323-332 10.1038/nature07370
    • (2008) Nature , vol.455 , pp. 323-332
    • Mohr, J.T.1    Krout, M.R.2    Stoltz, B.M.3
  • 10
    • 84890020560 scopus 로고    scopus 로고
    • Industrial Natural Product Chemistry for Drug Discovery and Development
    • Bauer, A.; Brönstrup, M. Industrial Natural Product Chemistry for Drug Discovery and Development Nat. Prod. Rep. 2014, 31, 35-60 10.1039/C3NP70058E
    • (2014) Nat. Prod. Rep. , vol.31 , pp. 35-60
    • Bauer, A.1    Brönstrup, M.2
  • 11
    • 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 10.1002/1521-3773(20010601)40:112004::AID-ANIE20043.0.CO;2-5
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 12
    • 77949786732 scopus 로고    scopus 로고
    • In Situ Click Chemistry: Probing the Binding Landscapes of Biological Molecules
    • Mamidyala, S. K.; Finn, M. G. In Situ Click Chemistry: Probing the Binding Landscapes of Biological Molecules Chem. Soc. Rev. 2010, 39, 1252-1261 10.1039/b901969n
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1252-1261
    • Mamidyala, S.K.1    Finn, M.G.2
  • 13
    • 34447562439 scopus 로고    scopus 로고
    • In Situ Click Chemistry: A Powerful Means for Lead Discovery
    • Sharpless, K. B.; Manetsch, R. In Situ Click Chemistry: a Powerful Means for Lead Discovery Expert Opin. Drug Discovery 2006, 1, 525-538 10.1517/17460441.1.6.525
    • (2006) Expert Opin. Drug Discovery , vol.1 , pp. 525-538
    • Sharpless, K.B.1    Manetsch, R.2
  • 14
    • 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 10.1002/1521-3773(20020715)41:142596::AID-ANIE25963.0.CO;2-4
    • (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
  • 15
    • 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 10.1021/jo011148j
    • (2002) J. Org. Chem. , vol.67 , pp. 3057-3064
    • Tornøe, C.W.1    Christensen, C.2    Meldal, M.3
  • 16
    • 34848920359 scopus 로고    scopus 로고
    • Peptidotriazoles: Copper(I)-catalyzed 1,3-Dipolar Cycloadditions on Solid-phase in Peptides
    • The first example of Cu(I) catalysed 1,3-Huisgen cycloaddition was reported in 2001 by Meldal; see; Lebl, M. Houghten, R. A. American Peptide Society and Kluwer Academic Publishers: San Diego
    • The first example of Cu(I) catalysed 1,3-Huisgen cycloaddition was reported in 2001 by Meldal; see Tornøe, C. W.; Meldal, M. Peptidotriazoles: Copper(I)-catalyzed 1,3-Dipolar Cycloadditions on Solid-phase in Peptides. Proc. Am. Pept. Symp. Lebl, M.; Houghten, R. A., Eds.; American Peptide Society and Kluwer Academic Publishers: San Diego, 2001; pp 263-264.
    • (2001) Proc. Am. Pept. Symp. , pp. 263-264
    • Tornøe, C.W.1    Meldal, M.2
  • 19
    • 80053528741 scopus 로고    scopus 로고
    • Click Chemistry: 1,2,3-Triazoles as Pharmacophores
    • Agalave, S. G.; Maujan, S. R.; Pore, V. S. Click Chemistry: 1,2,3-Triazoles as Pharmacophores Chem.-Asian J. 2011, 6, 2696-2718 10.1002/asia.201100432
    • (2011) Chem. - Asian J. , vol.6 , pp. 2696-2718
    • Agalave, S.G.1    Maujan, S.R.2    Pore, V.S.3
  • 20
    • 34547272503 scopus 로고    scopus 로고
    • The Growing Applications of Click Chemistry
    • Moses, J. E.; Moorhouse, A. D. The Growing Applications of Click Chemistry Chem. Soc. Rev. 2007, 36, 1249-1262 10.1039/b613014n
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1249-1262
    • Moses, J.E.1    Moorhouse, A.D.2
  • 21
    • 51049094897 scopus 로고    scopus 로고
    • Cu-catalyzed Azide-alkyne Cycloaddition
    • Meldal, M.; Tornøe, C. W. Cu-catalyzed Azide-alkyne Cycloaddition Chem. Rev. 2008, 108, 2952-3015 10.1021/cr0783479
    • (2008) Chem. Rev. , vol.108 , pp. 2952-3015
    • Meldal, M.1    Tornøe, C.W.2
  • 24
    • 84861499417 scopus 로고    scopus 로고
    • The Impact of Click Chemistry in Medicinal Chemistry
    • Hou, J.; Liu, X.; Shen, J.; Zhao, G.; Wang, P. G. The Impact of Click Chemistry in Medicinal Chemistry Expert Opin. Drug Discovery 2012, 7, 489-501 10.1517/17460441.2012.682725
    • (2012) Expert Opin. Drug Discovery , vol.7 , pp. 489-501
    • Hou, J.1    Liu, X.2    Shen, J.3    Zhao, G.4    Wang, P.G.5
  • 25
    • 84867726453 scopus 로고    scopus 로고
    • I-Catalyzed Alkyne-Azide "Click" Cycloadditions from a Mechanistic and Synthetic Perspective
    • I-Catalyzed Alkyne-Azide "Click" Cycloadditions from a Mechanistic and Synthetic Perspective Eur. J. Org. Chem. 2006, 2006, 51-68 10.1002/ejoc.200500483
    • (2006) Eur. J. Org. Chem. , vol.2006 , pp. 51-68
    • Bock, V.D.1    Hiemstra, H.2    Van Maarseveen, J.H.3
  • 26
    • 84876676322 scopus 로고    scopus 로고
    • Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-catalyzed Azide-alkyne Cycloadditions
    • Worrell, B. T.; Malik, J. A.; Fokin, V. V. Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-catalyzed Azide-alkyne Cycloadditions Science 2013, 340, 457-460 10.1126/science.1229506
    • (2013) Science , vol.340 , pp. 457-460
    • Worrell, B.T.1    Malik, J.A.2    Fokin, V.V.3
  • 27
    • 39549111477 scopus 로고    scopus 로고
    • Click Chemistry Reactions in Medicinal Chemistry: Applications of the 1,3-Dipolar Cycloaddition between Azides and Alkynes
    • Tron, G. C.; Pirali, T.; Billington, R. A.; Canonico, P. L.; Sorba, G.; Genazzani, A. A. Click Chemistry Reactions in Medicinal Chemistry: Applications of the 1,3-Dipolar Cycloaddition Between Azides and Alkynes Med. Res. Rev. 2008, 28, 278-308 10.1002/med.20107
    • (2008) Med. Res. Rev. , vol.28 , pp. 278-308
    • Tron, G.C.1    Pirali, T.2    Billington, R.A.3    Canonico, P.L.4    Sorba, G.5    Genazzani, A.A.6
  • 28
    • 84877835595 scopus 로고    scopus 로고
    • Click Chemistry for Drug Development and Diverse Chemical-biology Applications
    • Thirumurugan, P.; Matosiuk, D.; Jozwiak, K. Click Chemistry for Drug Development and Diverse Chemical-biology Applications Chem. Rev. 2013, 113, 4905-4979 10.1021/cr200409f
    • (2013) Chem. Rev. , vol.113 , pp. 4905-4979
    • Thirumurugan, P.1    Matosiuk, D.2    Jozwiak, K.3
  • 29
    • 43449108552 scopus 로고    scopus 로고
    • Efficient Construction of Therapeutics, Bioconjugates, Biomaterials and Bioactive Surfaces Using Azide-alkyne "Click" Chemistry
    • Lutz, J. F.; Zarafshani, Z. Efficient Construction of Therapeutics, Bioconjugates, Biomaterials and Bioactive Surfaces Using Azide-alkyne "Click" Chemistry Adv. Drug Delivery Rev. 2008, 60, 958-970 10.1016/j.addr.2008.02.004
    • (2008) Adv. Drug Delivery Rev. , vol.60 , pp. 958-970
    • Lutz, J.F.1    Zarafshani, Z.2
  • 30
    • 47649133089 scopus 로고    scopus 로고
    • Click Chemistry and Medicinal Chemistry: A Case of "Cyclo-addiction"
    • Moorhouse, A. D.; Moses, J. E. Click Chemistry and Medicinal Chemistry: a Case of "Cyclo-addiction" ChemMedChem 2008, 3, 715-723 10.1002/cmdc.200700334
    • (2008) ChemMedChem , vol.3 , pp. 715-723
    • Moorhouse, A.D.1    Moses, J.E.2
  • 31
    • 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 10.1016/S1359-6446(03)02933-7
    • (2003) Drug Discovery Today , vol.8 , pp. 1128-1137
    • Kolb, H.C.1    Sharpless, K.B.2
  • 32
    • 84873122458 scopus 로고    scopus 로고
    • Click Reaction in Carbohydrate Chemistry: Recent Developments and Future Perspective
    • Kushwaha, D.; Dwivedi, P.; Kuanar, S. K.; Tiwari, V. K. Click Reaction in Carbohydrate Chemistry: Recent Developments and Future Perspective Curr. Org. Synth. 2013, 10, 90-135 10.2174/1570179411310010005
    • (2013) Curr. Org. Synth. , vol.10 , pp. 90-135
    • Kushwaha, D.1    Dwivedi, P.2    Kuanar, S.K.3    Tiwari, V.K.4
  • 35
    • 82955165019 scopus 로고    scopus 로고
    • "Clicking" on/with Polymers: A Rapidly Expanding Field for the Straightforward Preparation of Novel Macromolecular Architectures
    • Kempe, K.; Krieg, A.; Becer, C. R.; Schubert, U. S. "Clicking" on/with Polymers: a Rapidly Expanding Field for the Straightforward Preparation of Novel Macromolecular Architectures Chem. Soc. Rev. 2012, 41, 176-191 10.1039/C1CS15107J
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 176-191
    • Kempe, K.1    Krieg, A.2    Becer, C.R.3    Schubert, U.S.4
  • 36
    • 80053495135 scopus 로고    scopus 로고
    • Fabrication and Functionalization of Hydrogels through "Click" Chemistry
    • Yigit, S.; Sanyal, R.; Sanyal, A. Fabrication and Functionalization of Hydrogels through "Click" Chemistry Chem.-Asian J. 2011, 6, 2648-2659 10.1002/asia.201100440
    • (2011) Chem. - Asian J. , vol.6 , pp. 2648-2659
    • Yigit, S.1    Sanyal, R.2    Sanyal, A.3
  • 37
    • 77949812304 scopus 로고    scopus 로고
    • Marrying Click Chemistry with Polymerization: Expanding the Scope of Polymeric Materials
    • Golas, P. L.; Matyjaszewski, K. Marrying Click Chemistry with Polymerization: Expanding the Scope of Polymeric Materials Chem. Soc. Rev. 2010, 39, 1338-1354 10.1039/B901978M
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1338-1354
    • Golas, P.L.1    Matyjaszewski, K.2
  • 38
    • 33846703461 scopus 로고    scopus 로고
    • "Click" Chemistry in Polymer and Materials Science
    • Binder, W. H.; Sachsenhofer, R. "Click" Chemistry in Polymer and Materials Science Macromol. Rapid Commun. 2007, 28, 15-54 10.1002/marc.200600625
    • (2007) Macromol. Rapid Commun. , vol.28 , pp. 15-54
    • Binder, W.H.1    Sachsenhofer, R.2
  • 39
    • 34548639157 scopus 로고    scopus 로고
    • Click Chemistry: Versatility and Control in the Hands of Materials Scientists
    • Nandivada, H.; Jiang, X.; Lahann, J. Click Chemistry: Versatility and Control in the Hands of Materials Scientists Adv. Mater. 2007, 19, 2197-2208 10.1002/adma.200602739
    • (2007) Adv. Mater. , vol.19 , pp. 2197-2208
    • Nandivada, H.1    Jiang, X.2    Lahann, J.3
  • 41
    • 34547482973 scopus 로고    scopus 로고
    • Clicking Polymers: A Straightforward Approach to Novel Macromolecular Architectures
    • Fournier, D.; Hoogenboom, R.; Schubert, U. S. Clicking Polymers: a Straightforward Approach to Novel Macromolecular Architectures Chem. Soc. Rev. 2007, 36, 1369-1380 10.1039/b700809k
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1369-1380
    • Fournier, D.1    Hoogenboom, R.2    Schubert, U.S.3
  • 42
    • 77949799806 scopus 로고    scopus 로고
    • Click Chemistry under Non-classical Reaction Conditions
    • Kappe, C. O.; Van Der Eycken, E. Click Chemistry under Non-classical Reaction Conditions Chem. Soc. Rev. 2010, 39, 1280-1290 10.1039/B901973C
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1280-1290
    • Kappe, C.O.1    Van Der Eycken, E.2
  • 45
    • 84855856535 scopus 로고    scopus 로고
    • Triterpenoids for Cancer Prevention and Treatment: Current Status and Future Prospects
    • Patlolla, J. M. R.; Rao, C. V. Triterpenoids for Cancer Prevention and Treatment: Current Status and Future Prospects Curr. Pharm. Biotechnol. 2012, 13, 147-155 10.2174/138920112798868719
    • (2012) Curr. Pharm. Biotechnol. , vol.13 , pp. 147-155
    • Patlolla, J.M.R.1    Rao, C.V.2
  • 46
    • 0027074951 scopus 로고
    • Steroid Research at Syntex: "The Pill" and Cortisone
    • Djerassi, C. Steroid Research at Syntex: "the Pill" and Cortisone Steroids 1992, 57, 631-641 10.1016/0039-128X(92)90016-3
    • (1992) Steroids , vol.57 , pp. 631-641
    • Djerassi, C.1
  • 47
    • 77957155737 scopus 로고    scopus 로고
    • Trends for Diverse Production Strategies of Plant Medicinal Alkaloids
    • Yang, L.; Stöckigt, J. Trends for Diverse Production Strategies of Plant Medicinal Alkaloids Nat. Prod. Rep. 2010, 27, 1469-1479 10.1039/c005378c
    • (2010) Nat. Prod. Rep. , vol.27 , pp. 1469-1479
    • Yang, L.1    Stöckigt, J.2
  • 49
    • 77950521746 scopus 로고    scopus 로고
    • Cinchona Alkaloids in Asymmetric Organocatalysis
    • Marcelli, T.; Hiemstra, H. Cinchona Alkaloids in Asymmetric Organocatalysis Synthesis 2010, 8, 1229-1279 10.1055/s-0029-1218699
    • (2010) Synthesis , vol.8 , pp. 1229-1279
    • Marcelli, T.1    Hiemstra, H.2
  • 50
    • 79951680836 scopus 로고    scopus 로고
    • Recent Applications of Cinchona Alkaloids and Their Derivatives as Catalysts in Metal-free Asymmetric Synthesis
    • Yeboah, E. M. O.; Yeboah, S. O.; Singh, G. S. Recent Applications of Cinchona Alkaloids and Their Derivatives as Catalysts in Metal-free Asymmetric Synthesis Tetrahedron 2011, 67, 1725-1762 10.1016/j.tet.2010.12.050
    • (2011) Tetrahedron , vol.67 , pp. 1725-1762
    • Yeboah, E.M.O.1    Yeboah, S.O.2    Singh, G.S.3
  • 51
    • 84864668043 scopus 로고    scopus 로고
    • Resolution of Racemates and Enantioselective Analytics by Cinchona Alkaloids and Their Derivatives
    • Song, Ch. E. Wiley-VCH: Weinheim, Chapter 13
    • Kacprzak, K.; Gawroński, J. Resolution of Racemates and Enantioselective Analytics by Cinchona Alkaloids and Their Derivatives. In Cinchona Alkaloids in Synthesis and Catalysis, Song, Ch. E., Ed.; Wiley-VCH: Weinheim, 2009; Chapter 13.
    • (2009) Cinchona Alkaloids in Synthesis and Catalysis
    • Kacprzak, K.1    Gawroński, J.2
  • 52
    • 34848865280 scopus 로고    scopus 로고
    • Bile Acid Scaffolds in Supramolecular Chemistry: The Interplay of Design and Synthesis
    • Davis, A. P. Bile Acid Scaffolds in Supramolecular Chemistry: the Interplay of Design and Synthesis Molecules 2007, 12, 2106-2122 10.3390/12082106
    • (2007) Molecules , vol.12 , pp. 2106-2122
    • Davis, A.P.1
  • 53
    • 77957789362 scopus 로고    scopus 로고
    • Steroid-based Anion Receptors and Transporters
    • Brotherhood, P. R.; Davis, A. P. Steroid-based Anion Receptors and Transporters Chem. Soc. Rev. 2010, 39, 3633-3647 10.1039/b926225n
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 3633-3647
    • Brotherhood, P.R.1    Davis, A.P.2
  • 54
    • 33750502923 scopus 로고    scopus 로고
    • Anion Binding and Transport by Steroid-based Receptors
    • Davis, A. P. Anion Binding and Transport by Steroid-based Receptors Coord. Chem. Rev. 2006, 250, 2939-2951 10.1016/j.ccr.2006.05.008
    • (2006) Coord. Chem. Rev. , vol.250 , pp. 2939-2951
    • Davis, A.P.1
  • 55
    • 0037227252 scopus 로고    scopus 로고
    • Development of Cholesterol-based Conjugates for Targeted Drug Delivery
    • Alanazi, F.; Halpern, D. S.; Lu, D. R. Development of Cholesterol-based Conjugates for Targeted Drug Delivery STP Pharm. Sci. 2003, 13, 27-35
    • (2003) STP Pharm. Sci. , vol.13 , pp. 27-35
    • Alanazi, F.1    Halpern, D.S.2    Lu, D.R.3
  • 56
    • 80053515989 scopus 로고    scopus 로고
    • Steroid/triterpenoid Functional Molecules Based on "Click Chemistry"
    • Hu, J.; Lu, J. R.; Ju, Y. Steroid/triterpenoid Functional Molecules Based on "Click Chemistry" Chem.-Asian J. 2011, 6, 2636-2647 10.1002/asia.201100378
    • (2011) Chem. - Asian J. , vol.6 , pp. 2636-2647
    • Hu, J.1    Lu, J.R.2    Ju, Y.3
  • 57
  • 58
    • 0034063289 scopus 로고    scopus 로고
    • Synthesis of 10,11-Didehydro Cinchona Alkaloids and Key Derivatives
    • Braje, W. M.; Frackenpohl, J.; Schrake, O.; Wartchow, R.; Beil, W.; Hoffmann, H. M. R. Synthesis of 10,11-Didehydro Cinchona Alkaloids and Key Derivatives Helv. Chim. Acta 2000, 83, 777-792 10.1002/(SICI)1522-2675(20000412)83:4777::AID-HLCA7773.3.CO;2-N
    • (2000) Helv. Chim. Acta , vol.83 , pp. 777-792
    • Braje, W.M.1    Frackenpohl, J.2    Schrake, O.3    Wartchow, R.4    Beil, W.5    Hoffmann, H.M.R.6
  • 59
    • 39749164489 scopus 로고    scopus 로고
    • An Improved Synthesis of 10,11-Didehydro Cinchona Alkaloids
    • Kacprzak, K. M.; Lindner, W.; Maier, N. M. An Improved Synthesis of 10,11-Didehydro Cinchona Alkaloids Chirality 2008, 20, 441-445 10.1002/chir.20461
    • (2008) Chirality , vol.20 , pp. 441-445
    • Kacprzak, K.M.1    Lindner, W.2    Maier, N.M.3
  • 60
    • 33750492630 scopus 로고    scopus 로고
    • Highly Efficient Immobilization of Cinchona Alkaloid Derivatives to Silica Gel via Click Chemistry
    • Kacprzak, K. M.; Maier, N. M.; Lindner, W. Highly Efficient Immobilization of Cinchona Alkaloid Derivatives to Silica Gel via Click Chemistry Tetrahedron Lett. 2006, 47, 8721-8726 10.1016/j.tetlet.2006.10.018
    • (2006) Tetrahedron Lett. , vol.47 , pp. 8721-8726
    • Kacprzak, K.M.1    Maier, N.M.2    Lindner, W.3
  • 61
    • 79951720434 scopus 로고    scopus 로고
    • Triazolo-linked Cinchona Alkaloid Carbamate Anion Exchange-type Chiral Stationary Phases: Synthesis by Click Chemistry and Evaluation
    • Kacprzak, K. M.; Maier, N. M.; Lindner, W. Triazolo-linked Cinchona Alkaloid Carbamate Anion Exchange-type Chiral Stationary Phases: Synthesis by Click Chemistry and Evaluation J. Chromatogr. A 2011, 1218, 1452-1460 10.1016/j.chroma.2011.01.031
    • (2011) J. Chromatogr. A , vol.1218 , pp. 1452-1460
    • Kacprzak, K.M.1    Maier, N.M.2    Lindner, W.3
  • 62
    • 77956907286 scopus 로고    scopus 로고
    • Unexpected Enantioseparation of Mandelic Acids and Their Derivatives on 1,2,3-Triazololinked Quinine tert-Butyl Carbamate Anion Exchange-type Chiral Stationary Phase
    • Kacprzak, K. M.; Maier, N. M.; Lindner, W. Unexpected Enantioseparation of Mandelic Acids and Their Derivatives on 1,2,3-Triazololinked Quinine tert-Butyl Carbamate Anion Exchange-type Chiral Stationary Phase J. Sep. Sci. 2010, 33, 2590-2598 10.1002/jssc.201000393
    • (2010) J. Sep. Sci. , vol.33 , pp. 2590-2598
    • Kacprzak, K.M.1    Maier, N.M.2    Lindner, W.3
  • 63
    • 80052795489 scopus 로고    scopus 로고
    • Novel Pirkle-type Quinine 3,5-Dinitrophenylcarbamate Chiral Stationary Phase Implementing Click Chemistry
    • Kacprzak, K. M.; Lindner, W. Novel Pirkle-type Quinine 3,5-Dinitrophenylcarbamate Chiral Stationary Phase Implementing Click Chemistry J. Sep. Sci. 2011, 34, 2391-2396 10.1002/jssc.201100395
    • (2011) J. Sep. Sci. , vol.34 , pp. 2391-2396
    • Kacprzak, K.M.1    Lindner, W.2
  • 64
    • 84900627864 scopus 로고    scopus 로고
    • Novel Carbamoyl Type Quinine and Quinidine Based Chiral Anion Exchangers Implementing Alkyne-azide Cycloaddition Immobilization Chemistry
    • Hettegger, H.; Kohout, M.; Mimini, V.; Lindner, W. Novel Carbamoyl Type Quinine and Quinidine Based Chiral Anion Exchangers Implementing Alkyne-azide Cycloaddition Immobilization Chemistry J. Chromatogr. A 2014, 1337, 85-94 10.1016/j.chroma.2014.02.026
    • (2014) J. Chromatogr. A , vol.1337 , pp. 85-94
    • Hettegger, H.1    Kohout, M.2    Mimini, V.3    Lindner, W.4
  • 65
    • 23344445780 scopus 로고    scopus 로고
    • Fluorous Click Chemistry as a Practical Tagging Method
    • Kaleta, Z.; Egyed, O.; Soós, T. Fluorous Click Chemistry as a Practical Tagging Method Org. Biomol. Chem. 2005, 3, 2228-2230 10.1039/b504973c
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 2228-2230
    • Kaleta, Z.1    Egyed, O.2    Soós, T.3
  • 66
    • 77954303369 scopus 로고    scopus 로고
    • Simple Preparation of Dimeric Cinchona Alkaloid Derivatives on Polystyrene Supports and a Highly Enantioselective Catalytic Heterogeneous Dimerization of Ketenes
    • Jumde, R. P.; Mandoli, A.; De Lorenzi, F.; Pini, D.; Salvadori, P. Simple Preparation of Dimeric Cinchona Alkaloid Derivatives on Polystyrene Supports and a Highly Enantioselective Catalytic Heterogeneous Dimerization of Ketenes Adv. Synth. Catal. 2010, 352, 1434-1440 10.1002/adsc.201000165
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 1434-1440
    • Jumde, R.P.1    Mandoli, A.2    De Lorenzi, F.3    Pini, D.4    Salvadori, P.5
  • 67
    • 84921628665 scopus 로고    scopus 로고
    • New Polymer-supported Mono- and bis-Cinchona Alkaloid Derivatives: Synthesis and Use in Asymmetric Organocatalyzed Reactions
    • Jumde, R. P.; Di Pietro, A.; Manariti, A.; Mandoli, A. New Polymer-supported Mono- and bis-Cinchona Alkaloid Derivatives: Synthesis and Use in Asymmetric Organocatalyzed Reactions Chem.-Asian J. 2015, 10, 397-404 10.1002/asia.201402924
    • (2015) Chem. - Asian J. , vol.10 , pp. 397-404
    • Jumde, R.P.1    Di Pietro, A.2    Manariti, A.3    Mandoli, A.4
  • 68
    • 84929466905 scopus 로고    scopus 로고
    • Comparison of Different Polymer- and Silica-supported 9-Amino-9-deoxy-epi-quinines as Recyclable Organocatalysts
    • Porta, R.; Coccia, F.; Annunziata, R.; Puglisi, A. Comparison of Different Polymer- and Silica-supported 9-Amino-9-deoxy-epi-quinines as Recyclable Organocatalysts ChemCatChem 2015, 7, 1490-1499 10.1002/cctc.201500106
    • (2015) ChemCatChem , vol.7 , pp. 1490-1499
    • Porta, R.1    Coccia, F.2    Annunziata, R.3    Puglisi, A.4
  • 69
    • 84925813799 scopus 로고    scopus 로고
    • A Polystyrene-supported 9-Amino(9-deoxy)epiquinine Derivative for Continuous Flow Asymmetric Michael Reactions
    • Izquierdo, J.; Ayats, C.; Henseler, A. H.; Pericàs, M. A. A Polystyrene-supported 9-Amino(9-deoxy)epiquinine Derivative for Continuous Flow Asymmetric Michael Reactions Org. Biomol. Chem. 2015, 13, 4204-4209 10.1039/C5OB00325C
    • (2015) Org. Biomol. Chem. , vol.13 , pp. 4204-4209
    • Izquierdo, J.1    Ayats, C.2    Henseler, A.H.3    Pericàs, M.A.4
  • 70
    • 84922680029 scopus 로고    scopus 로고
    • Solid Supported 9-Amino-9-deoxy-epi-quinine as Efficient Organocatalyst for Stereoselective Reactions in Batch and under Continuous Flow Conditions
    • Porta, R.; Benaglia, M.; Coccia, F.; Cozzi, F.; Puglisi, A. Solid Supported 9-Amino-9-deoxy-epi-quinine as Efficient Organocatalyst for Stereoselective Reactions in Batch and Under Continuous Flow Conditions Adv. Synth. Catal. 2015, 357, 377-383 10.1002/adsc.201400821
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 377-383
    • Porta, R.1    Benaglia, M.2    Coccia, F.3    Cozzi, F.4    Puglisi, A.5
  • 71
    • 78651240030 scopus 로고    scopus 로고
    • Synthesis of 3′-Azido-3′-deoxythymidine (AZT) - Cinchona Alkaloid Conjugates via Click Chemistry: Toward Novel Fluorescent Markers and Cytostatic Agents
    • Baraniak, B.; Kacprzak, K.; Celewicz, L. Synthesis of 3′-Azido-3′-deoxythymidine (AZT)-Cinchona Alkaloid Conjugates via Click Chemistry: Toward Novel Fluorescent Markers and Cytostatic Agents Bioorg. Med. Chem. Lett. 2011, 21, 723-726 10.1016/j.bmcl.2010.11.127
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 723-726
    • Baraniak, B.1    Kacprzak, K.2    Celewicz, L.3
  • 72
    • 78649831810 scopus 로고    scopus 로고
    • Clickable 9-Azido-(9-deoxy)-Cinchona Alkaloids: Synthesis and Conformation
    • Kacprzak, K.; Gierczyk, B. Clickable 9-Azido-(9-deoxy)-Cinchona Alkaloids: Synthesis and Conformation Tetrahedron: Asymmetry 2010, 21, 2740-2745 10.1016/j.tetasy.2010.10.023
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 2740-2745
    • Kacprzak, K.1    Gierczyk, B.2
  • 73
    • 84877115441 scopus 로고    scopus 로고
    • Diastereoselective Corey-Chaykovsky 9-Epoxymethylation of Cinchona Alkaloids: Access to Chiral Scaffolds with Diverse Functionalities
    • Boratyński, P. J.; Skarzewski, J. Diastereoselective Corey-Chaykovsky 9-Epoxymethylation of Cinchona Alkaloids: Access to Chiral Scaffolds with Diverse Functionalities J. Org. Chem. 2013, 78, 4473-4482 10.1021/jo400465a
    • (2013) J. Org. Chem. , vol.78 , pp. 4473-4482
    • Boratyński, P.J.1    Skarzewski, J.2
  • 74
    • 31344479794 scopus 로고    scopus 로고
    • The Library of Cinchona Alkaloids-1,2,3-triazole Derivatives: Structure and Facile Access by "Click Chemistry"
    • Kacprzak, K.; Migas, M.; Plutecka, A.; Rychlewska, U.; Gawroński, J. The Library of Cinchona Alkaloids-1,2,3-triazole Derivatives: Structure and Facile Access by "Click Chemistry" Heterocycles 2005, 65, 1931-1938 10.3987/COM-05-10378
    • (2005) Heterocycles , vol.65 , pp. 1931-1938
    • Kacprzak, K.1    Migas, M.2    Plutecka, A.3    Rychlewska, U.4    Gawroński, J.5
  • 76
    • 0141631798 scopus 로고    scopus 로고
    • Fused Triazoles via Tandem Reactions of Activated Cinchona Alkaloids with Azide Ion. Second Cinchona Rearrangement Exemplified
    • Röper, S.; Franz, M. H.; Wartchow, R.; Hoffmann, H. M. Fused Triazoles via Tandem Reactions of Activated Cinchona Alkaloids with Azide Ion. Second Cinchona Rearrangement Exemplified Org. Lett. 2003, 5, 2773-2776 10.1021/ol034719y
    • (2003) Org. Lett. , vol.5 , pp. 2773-2776
    • Röper, S.1    Franz, M.H.2    Wartchow, R.3    Hoffmann, H.M.4
  • 77
    • 84862201122 scopus 로고    scopus 로고
    • Click Chemistry-derived Bivalent Quinine Inhibitors of P-glycoprotein-mediated Cellular Efflux
    • Kuriakose, J.; Hrycyna, C. A.; Chmielewski, J. Click Chemistry-derived Bivalent Quinine Inhibitors of P-glycoprotein-mediated Cellular Efflux Bioorg. Med. Chem. Lett. 2012, 22, 4410-4412 10.1016/j.bmcl.2012.04.125
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 4410-4412
    • Kuriakose, J.1    Hrycyna, C.A.2    Chmielewski, J.3
  • 79
    • 33846439358 scopus 로고    scopus 로고
    • Soluble Camptothecin Derivatives Prepared by Click Cycloaddition Chemistry on Functional Aliphatic Polyesters
    • Parrish, B.; Emrick, T. Soluble Camptothecin Derivatives Prepared by Click Cycloaddition Chemistry on Functional Aliphatic Polyesters Bioconjugate Chem. 2007, 18, 263-267 10.1021/bc060201d
    • (2007) Bioconjugate Chem. , vol.18 , pp. 263-267
    • Parrish, B.1    Emrick, T.2
  • 80
  • 81
    • 72449201610 scopus 로고    scopus 로고
    • Polymeric Phosphorylcholine-Camptothecin Conjugates Prepared by Controlled Free Radical Polymerization and Click Chemistry
    • Chen, X.; McRae, S.; Parelkar, S.; Emrick, T. Polymeric Phosphorylcholine-Camptothecin Conjugates Prepared by Controlled Free Radical Polymerization and Click Chemistry Bioconjugate Chem. 2009, 20, 2331-2341 10.1021/bc900339x
    • (2009) Bioconjugate Chem. , vol.20 , pp. 2331-2341
    • Chen, X.1    McRae, S.2    Parelkar, S.3    Emrick, T.4
  • 82
    • 32644453360 scopus 로고    scopus 로고
    • Copper-free Sonogashira Reaction using 7-Chloro Camptothecins
    • Luo, Y.; Gao, H.; Li, Y.; Huang, W.; Lu, W.; Zhang, Z. Copper-free Sonogashira Reaction using 7-Chloro Camptothecins Tetrahedron 2006, 62, 2465-2470 10.1016/j.tet.2006.01.001
    • (2006) Tetrahedron , vol.62 , pp. 2465-2470
    • Luo, Y.1    Gao, H.2    Li, Y.3    Huang, W.4    Lu, W.5    Zhang, Z.6
  • 83
    • 84894498565 scopus 로고    scopus 로고
    • Synthesis of 7-Triazole-substituted Camptothecin via Click Chemistry and Evaluation of in vitro Antitumor Activity
    • Wang, L.; Yuan, W.; Zhang, J.; Tong, L.; Luo, Y.; Chen, Y.; Lu, W.; Huang, Q. Synthesis of 7-Triazole-substituted Camptothecin via Click Chemistry and Evaluation of in vitro Antitumor Activity Chin. J. Chem. 2014, 32, 157-162 10.1002/cjoc.201300703
    • (2014) Chin. J. Chem. , vol.32 , pp. 157-162
    • Wang, L.1    Yuan, W.2    Zhang, J.3    Tong, L.4    Luo, Y.5    Chen, Y.6    Lu, W.7    Huang, Q.8
  • 84
    • 77951694589 scopus 로고    scopus 로고
    • Azides Derived from Colchicine and Their Use in Library Synthesis: A Practical Entry to New Bioactive Derivatives of an Old Natural Drug
    • Nicolaus, N.; Zapke, J.; Riesterer, P.; Neudörfl, J.-M.; Prokop, A.; Oschkinat, H.; Schmalz, H.-G. Azides Derived from Colchicine and Their Use in Library Synthesis: A Practical Entry to New Bioactive Derivatives of an Old Natural Drug ChemMedChem 2010, 5, 661-665 10.1002/cmdc.201000063
    • (2010) ChemMedChem , vol.5 , pp. 661-665
    • Nicolaus, N.1    Zapke, J.2    Riesterer, P.3    Neudörfl, J.-M.4    Prokop, A.5    Oschkinat, H.6    Schmalz, H.-G.7
  • 85
    • 79952774430 scopus 로고    scopus 로고
    • A Convenient Entry to New C-7-modified Colchicinoids Through Azide Alkyne [3 + 2] Cycloaddition: Application of Ring-contractive Rearangements
    • Nicolaus, N.; Reball, J.; Sitnikov, N.; Velder, J.; Termath, A.; Fedorov, A. Yu.; Schmalz, H.-G. A Convenient Entry to New C-7-modified Colchicinoids Through Azide Alkyne [3 + 2] Cycloaddition: Application of Ring-contractive Rearangements Heterocycles 2010, 82, 1585-1600 10.3987/COM-10-S(E)117
    • (2010) Heterocycles , vol.82 , pp. 1585-1600
    • Nicolaus, N.1    Reball, J.2    Sitnikov, N.3    Velder, J.4    Termath, A.5    Fedorov, A.Yu.6    Schmalz, H.-G.7
  • 88
    • 79953228834 scopus 로고    scopus 로고
    • Synthesis, Biological Evaluation and Molecular Modeling of Novel Triazole-containing Berberine Derivatives as Acetylcholinesterase and β-amyloid Aggregation Inhibitors
    • Shi, A.; Huang, L.; Lu, C.; He, F.; Li, X. Synthesis, Biological Evaluation and Molecular Modeling of Novel Triazole-containing Berberine Derivatives as Acetylcholinesterase and β-amyloid Aggregation Inhibitors Bioorg. Med. Chem. 2011, 19, 2298-2305 10.1016/j.bmc.2011.02.025
    • (2011) Bioorg. Med. Chem. , vol.19 , pp. 2298-2305
    • Shi, A.1    Huang, L.2    Lu, C.3    He, F.4    Li, X.5
  • 89
    • 84905665478 scopus 로고    scopus 로고
    • Design, Synthesis, and Anticancer Activity of Novel Berberine Derivatives Prepared via CuAAC "Click" Chemistry as Potential Anticancer Agents
    • Jin, X.; Yan, T.-H.; Yan, L.; Li, Q.; Wang, R.-L.; Hu, Z.-L.; Jiang, Y.-Y.; Sun, Q.-Y.; Cao, Y.-B. Design, Synthesis, and Anticancer Activity of Novel Berberine Derivatives Prepared via CuAAC "Click" Chemistry as Potential Anticancer Agents Drug Des., Dev. Ther. 2014, 8, 1047-1059 10.2147/DDDT.S63228
    • (2014) Drug Des., Dev. Ther. , vol.8 , pp. 1047-1059
    • Jin, X.1    Yan, T.-H.2    Yan, L.3    Li, Q.4    Wang, R.-L.5    Hu, Z.-L.6    Jiang, Y.-Y.7    Sun, Q.-Y.8    Cao, Y.-B.9
  • 90
    • 78650240536 scopus 로고    scopus 로고
    • Click Chemistry and Biocatalysis for the Preparation of Pancratistatin Analogs
    • de la Sovera, V.; Bellomo, A.; Gonzalez, D. Click Chemistry and Biocatalysis for the Preparation of Pancratistatin Analogs Tetrahedron Lett. 2011, 52, 430-433 10.1016/j.tetlet.2010.11.084
    • (2011) Tetrahedron Lett. , vol.52 , pp. 430-433
    • De La Sovera, V.1    Bellomo, A.2    Gonzalez, D.3
  • 91
    • 84900986993 scopus 로고    scopus 로고
    • Design, Synthesis and Molecular Docking Studies of Novel N-Benzenesulfonyl-1,2,3,4-tetrahydroisoquinoline-based Triazoles with Potential Anticancer Activity
    • Pingaew, R.; Mandi, P.; Nantasenamat, C.; Prachayasittikul, S.; Ruchirawat, S.; Prachayasittikul, V. Design, Synthesis and Molecular Docking Studies of Novel N-Benzenesulfonyl-1,2,3,4-tetrahydroisoquinoline-based Triazoles with Potential Anticancer Activity Eur. J. Med. Chem. 2014, 81, 192-203 10.1016/j.ejmech.2014.05.019
    • (2014) Eur. J. Med. Chem. , vol.81 , pp. 192-203
    • Pingaew, R.1    Mandi, P.2    Nantasenamat, C.3    Prachayasittikul, S.4    Ruchirawat, S.5    Prachayasittikul, V.6
  • 92
    • 84873570152 scopus 로고    scopus 로고
    • Facile Synthesis of (1,2,3)-Triazole-Fused Isoindolines, Tetrahydroisoquinolines, Benzoazepines and Benzoazocines by Palladium-Copper Catalysed Heterocyclisation
    • Brahma, K.; Achari, B.; Chowdhury, C. Facile Synthesis of (1,2,3)-Triazole-Fused Isoindolines, Tetrahydroisoquinolines, Benzoazepines and Benzoazocines by Palladium-Copper Catalysed Heterocyclisation Synthesis 2013, 45, 545-555 10.1055/s-0032-1316839
    • (2013) Synthesis , vol.45 , pp. 545-555
    • Brahma, K.1    Achari, B.2    Chowdhury, C.3
  • 93
    • 80051889227 scopus 로고    scopus 로고
    • An Efficient Synthesis of a (-)-Physostigmine"s Library for Identifying Potential Anti-Alzheimer"s Agents
    • Wu, Y.; Wang, F.; Song, H.; Qin, Y. An Efficient Synthesis of a (-)-Physostigmine"s Library for Identifying Potential Anti-Alzheimer"s Agents Helv. Chim. Acta 2011, 94, 1496-1505 10.1002/hlca.201100020
    • (2011) Helv. Chim. Acta , vol.94 , pp. 1496-1505
    • Wu, Y.1    Wang, F.2    Song, H.3    Qin, Y.4
  • 94
    • 84885041416 scopus 로고    scopus 로고
    • Synthesis and Anticholinesterase Activity of (-)-Physostigmine Analogues with Modifications at C3α and C5
    • Wang, H. J.; Zhang, D.; Wang, F. S.; Wu, Y.; Song, H. Synthesis and Anticholinesterase Activity of (-)-Physostigmine Analogues with Modifications at C3α and C5 Chem. Res. Chin. Univ. 2013, 29, 888-893 10.1007/s40242-013-3066-y
    • (2013) Chem. Res. Chin. Univ. , vol.29 , pp. 888-893
    • Wang, H.J.1    Zhang, D.2    Wang, F.S.3    Wu, Y.4    Song, H.5
  • 95
    • 77949768135 scopus 로고    scopus 로고
    • Two Versatile and Parallel Approaches to Highly Symmetrical Open and Closed Natural Product-based Structures
    • Montenegro, H. E.; Ramírez-López, P.; de la Torre, M. C.; Asenjo, M.; Sierra, M. Two Versatile and Parallel Approaches to Highly Symmetrical Open and Closed Natural Product-based Structures Chem.-Eur. J. 2010, 16, 3798-3814 10.1002/chem.200903264
    • (2010) Chem. - Eur. J. , vol.16 , pp. 3798-3814
    • Montenegro, H.E.1    Ramírez-López, P.2    De La Torre, M.C.3    Asenjo, M.4    Sierra, M.5
  • 96
    • 79960362357 scopus 로고    scopus 로고
    • Flustramine Inspired Synthesis and Biological Evaluation of Pyrroloindoline Triazole Amides as Novel Inhibitors of Bacterial Biofilms
    • Bunders, C.; Cavanagh, J.; Melander, C. Flustramine Inspired Synthesis and Biological Evaluation of Pyrroloindoline Triazole Amides as Novel Inhibitors of Bacterial Biofilms Org. Biomol. Chem. 2011, 9, 5476-5481 10.1039/c1ob05605k
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 5476-5481
    • Bunders, C.1    Cavanagh, J.2    Melander, C.3
  • 98
    • 79953212266 scopus 로고    scopus 로고
    • Synthesis and Biological Activity of 2-Aminoimidazole Triazoles Accessed by Suzuki-Miyaura Cross-coupling
    • Reyes, S.; Huigens, R. W., III; Su, Z.; Simon, M. L.; Melander, C. Synthesis and Biological Activity of 2-Aminoimidazole Triazoles Accessed by Suzuki-Miyaura Cross-coupling Org. Biomol. Chem. 2011, 9, 3041-3049 10.1039/c0ob00925c
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 3041-3049
    • Reyes, S.1    Huigens, R.W.2    Su, Z.3    Simon, M.L.4    Melander, C.5
  • 99
    • 82955165642 scopus 로고    scopus 로고
    • Evaluation of 4,5-Disubstituted-2-aminoimidazole-triazole Conjugates for Antibiofilm/antibiotic Resensitization Activity Against MRSA and Acinetobacter Baumannii
    • Su, Z.; Peng, L.; Worthington, R. J.; Melander, C. Evaluation of 4,5-Disubstituted-2-aminoimidazole-triazole Conjugates for Antibiofilm/antibiotic Resensitization Activity Against MRSA and Acinetobacter Baumannii ChemMedChem 2011, 6, 2243-2251 10.1002/cmdc.201100316
    • (2011) ChemMedChem , vol.6 , pp. 2243-2251
    • Su, Z.1    Peng, L.2    Worthington, R.J.3    Melander, C.4
  • 100
    • 84872686801 scopus 로고    scopus 로고
    • A Flexible Approach to 1,4-Di-substituted 2-Aminoimidazoles That Inhibit and Disperse Biofilms and Potentiate the Effects of β-Lactams Against Multi-drug Resistant Bacteria
    • Furlani, R. E.; Yeagley, A. A.; Melander, C. A Flexible Approach to 1,4-Di-substituted 2-Aminoimidazoles That Inhibit and Disperse Biofilms and Potentiate the Effects of β-Lactams Against Multi-drug Resistant Bacteria Eur. J. Med. Chem. 2013, 62, 59-70 10.1016/j.ejmech.2012.12.005
    • (2013) Eur. J. Med. Chem. , vol.62 , pp. 59-70
    • Furlani, R.E.1    Yeagley, A.A.2    Melander, C.3
  • 101
    • 80054755092 scopus 로고    scopus 로고
    • Designing 2-Aminoimidazole Alkaloids Analogs with Anti-biofilm Activities: Structure-activities Relationships of Polysubstituted Triazoles
    • Linares, D.; Bottzeck, O.; Pereira, O.; Praud-Tabariès, A.; Blache, Y. Designing 2-Aminoimidazole Alkaloids Analogs with Anti-biofilm Activities: Structure-activities Relationships of Polysubstituted Triazoles Bioorg. Med. Chem. Lett. 2011, 21, 6751-6755 10.1016/j.bmcl.2011.09.050
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 6751-6755
    • Linares, D.1    Bottzeck, O.2    Pereira, O.3    Praud-Tabariès, A.4    Blache, Y.5
  • 102
    • 77949280828 scopus 로고    scopus 로고
    • Synthesis of Triazolyl-Substituted 3-Aminopiperidines by Huisgen-1,3-Dipolar Cycloaddition - New Scaffolds for Combinatorial Chemistry
    • Schramm, H.; Saak, W.; Hoenke, C.; Christoffers, J. Synthesis of Triazolyl-Substituted 3-Aminopiperidines by Huisgen-1,3-Dipolar Cycloaddition-New Scaffolds for Combinatorial Chemistry Eur. J. Org. Chem. 2010, 2010, 1745-1753 10.1002/ejoc.200901458
    • (2010) Eur. J. Org. Chem. , vol.2010 , pp. 1745-1753
    • Schramm, H.1    Saak, W.2    Hoenke, C.3    Christoffers, J.4
  • 103
    • 79951850432 scopus 로고    scopus 로고
    • Synthesis of trans-4 Triazolyl-Substituted 3-Hydroxypiperidines
    • Harmsen, R. A. G.; Sydnes, L.; Törnroos, K. W.; Haug, B. E. Synthesis of trans-4 Triazolyl-Substituted 3-Hydroxypiperidines Synthesis 2011, 2011, 749-754 10.1055/s-0030-1259569
    • (2011) Synthesis , vol.2011 , pp. 749-754
    • Harmsen, R.A.G.1    Sydnes, L.2    Törnroos, K.W.3    Haug, B.E.4
  • 104
    • 66349095655 scopus 로고    scopus 로고
    • Synthesis of Novel 3-(1-(1-Substituted Piperidin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-5(4H)-one as Antifungal Agents
    • Sangshetti, J. N.; Nagawade, R. R.; Shinde, D. B. Synthesis of Novel 3-(1-(1-Substituted Piperidin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-5(4H)-one as Antifungal Agents Bioorg. Med. Chem. Lett. 2009, 19, 3564-3567 10.1016/j.bmcl.2009.04.134
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 3564-3567
    • Sangshetti, J.N.1    Nagawade, R.R.2    Shinde, D.B.3
  • 105
    • 84879482779 scopus 로고    scopus 로고
    • A Novel Amalgamation of 1,2,3-Triazoles, Piperidines and Thieno Pyridine Rings and Evaluation of Their Antifungal Activity
    • Darandale, S. N.; Mulla, N. A.; Pansare, D. N.; Sangshetti, J. N.; Shinde, D. B. A Novel Amalgamation of 1,2,3-Triazoles, Piperidines and Thieno Pyridine Rings and Evaluation of Their Antifungal Activity Eur. J. Med. Chem. 2013, 65, 527-532 10.1016/j.ejmech.2013.04.045
    • (2013) Eur. J. Med. Chem. , vol.65 , pp. 527-532
    • Darandale, S.N.1    Mulla, N.A.2    Pansare, D.N.3    Sangshetti, J.N.4    Shinde, D.B.5
  • 106
    • 84896766412 scopus 로고    scopus 로고
    • One-pot Synthesis of 3-Azido- and 3-Aminopiperidines by Intramolecular Cyclization of Unsaturated Amines
    • Ortiz, G. X., Jr.; Kang, B.; Wang, Q. One-pot Synthesis of 3-Azido- and 3-Aminopiperidines by Intramolecular Cyclization of Unsaturated Amines J. Org. Chem. 2014, 79, 571-581 10.1021/jo4022666
    • (2014) J. Org. Chem. , vol.79 , pp. 571-581
    • Ortiz, G.X.1    Kang, B.2    Wang, Q.3
  • 107
    • 79959684303 scopus 로고    scopus 로고
    • Thiopurine Derivatives Containing Triazole and Steroid: Synthesis, Antimalarial and Antileishmanial Activities
    • Corrales, R. C. N. R.; de Souza, N. B.; Pinheiro, L. S.; Abramo, C.; Coimbra, E. S.; Da Silva, A. D. Thiopurine Derivatives Containing Triazole and Steroid: Synthesis, Antimalarial and Antileishmanial Activities Biomed. Pharmacother. 2011, 65, 198-203 10.1016/j.biopha.2010.10.013
    • (2011) Biomed. Pharmacother. , vol.65 , pp. 198-203
    • Corrales, R.C.N.R.1    De Souza, N.B.2    Pinheiro, L.S.3    Abramo, C.4    Coimbra, E.S.5    Da Silva, A.D.6
  • 108
    • 79958753408 scopus 로고    scopus 로고
    • Novel Purine-based Fluoroaryl-1,2,3-triazoles as Neuroprotecting Agents: Synthesis, Neuronal Cell Culture Investigations, and CDK5 Docking Studies
    • Nair, N.; Kudo, W.; Smith, M. A.; Abrol, R.; Goddard, W. A., III; Reddy, V. P. Novel Purine-based Fluoroaryl-1,2,3-triazoles as Neuroprotecting Agents: Synthesis, Neuronal Cell Culture Investigations, and CDK5 Docking Studies Bioorg. Med. Chem. Lett. 2011, 21, 3957-3961 10.1016/j.bmcl.2011.05.019
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 3957-3961
    • Nair, N.1    Kudo, W.2    Smith, M.A.3    Abrol, R.4    Goddard, W.A.5    Reddy, V.P.6
  • 109
    • 84901799830 scopus 로고    scopus 로고
    • Synthesis, Cytotoxicity, Antimicrobial and Anti-biofilm Activities of Novel Pyrazolo(3,4-b)pyridine and Pyrimidine Functionalized 1,2,3-Triazole Derivatives
    • Nagender, P.; Malla Reddy, G.; Naresh Kumar, R.; Poornachandra, Y.; Ganesh Kumar, C.; Narsaiah, B. Synthesis, Cytotoxicity, Antimicrobial and Anti-biofilm Activities of Novel Pyrazolo(3,4-b)pyridine and Pyrimidine Functionalized 1,2,3-Triazole Derivatives Bioorg. Med. Chem. Lett. 2014, 24, 2905-2908 10.1016/j.bmcl.2014.04.084
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 2905-2908
    • Nagender, P.1    Malla Reddy, G.2    Naresh Kumar, R.3    Poornachandra, Y.4    Ganesh Kumar, C.5    Narsaiah, B.6
  • 112
    • 84858697862 scopus 로고    scopus 로고
    • Semi-synthesis of Bioactive Fluorescent Analogues of the Cytotoxic Marine Alkaloid Discorhabdin C
    • Lam, C. F. C.; Giddens, A. C.; Chand, N.; Webb, V. L.; Copp, B. R. Semi-synthesis of Bioactive Fluorescent Analogues of the Cytotoxic Marine Alkaloid Discorhabdin C Tetrahedron 2012, 68, 3187-3194 10.1016/j.tet.2012.02.052
    • (2012) Tetrahedron , vol.68 , pp. 3187-3194
    • Lam, C.F.C.1    Giddens, A.C.2    Chand, N.3    Webb, V.L.4    Copp, B.R.5
  • 113
    • 84894053007 scopus 로고    scopus 로고
    • Design, Synthesis, and Anti-tobacco Mosaic Virus (TMV) Activity of Glycoconjugates of Phenanthroindolizidines Alkaloids
    • Wu, M.; Han, G.; Meng, C.; Wang, Z.; Liu, Y.; Wang, Q. Design, Synthesis, and Anti-tobacco Mosaic Virus (TMV) Activity of Glycoconjugates of Phenanthroindolizidines Alkaloids Mol. Diversity 2014, 18, 25-37 10.1007/s11030-013-9484-4
    • (2014) Mol. Diversity , vol.18 , pp. 25-37
    • Wu, M.1    Han, G.2    Meng, C.3    Wang, Z.4    Liu, Y.5    Wang, Q.6
  • 114
    • 43749095416 scopus 로고    scopus 로고
    • Synthesis and Receptor Binding Properties of 2β-alkynyl and 2β-(1,2,3-Triazol)substituted 3β-(Substituted phenyl)tropane Derivatives
    • Jin, C.; Navarro, H. A.; Carroll, F. I. Synthesis and Receptor Binding Properties of 2β-alkynyl and 2β-(1,2,3-Triazol)substituted 3β-(Substituted phenyl)tropane Derivatives Bioorg. Med. Chem. 2008, 16, 5529-5535 10.1016/j.bmc.2008.04.008
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 5529-5535
    • Jin, C.1    Navarro, H.A.2    Carroll, F.I.3
  • 115
    • 84880039178 scopus 로고    scopus 로고
    • Synthesis of Novel Derivatives of Murrayafoline A and Their Inhibitory Effect on LPS-stimulated Production of Pro-inflammatory Cytokines in Bone Marrow-derived Dendritic Cells
    • Thuy, T. T. T.; Cuong, N. M.; Toan, T. Q.; Thang, N. N.; Tai, B. H.; Nhiem, N. X.; Hong, H.-J.; Kim, S.; Legoupy, S.; Koh, Y. S.; Kim, Y. H. Synthesis of Novel Derivatives of Murrayafoline A and Their Inhibitory Effect on LPS-stimulated Production of Pro-inflammatory Cytokines in Bone Marrow-derived Dendritic Cells Arch. Pharmacal Res. 2013, 36, 832-839 10.1007/s12272-013-0100-z
    • (2013) Arch. Pharmacal Res. , vol.36 , pp. 832-839
    • Thuy, T.T.T.1    Cuong, N.M.2    Toan, T.Q.3    Thang, N.N.4    Tai, B.H.5    Nhiem, N.X.6    Hong, H.-J.7    Kim, S.8    Legoupy, S.9    Koh, Y.S.10    Kim, Y.H.11
  • 116
    • 43049107992 scopus 로고    scopus 로고
    • Unearthing the Roots of the Terpenome
    • Christianson, D. W. Unearthing the Roots of the Terpenome Curr. Opin. Chem. Biol. 2008, 12, 141-150 10.1016/j.cbpa.2007.12.008
    • (2008) Curr. Opin. Chem. Biol. , vol.12 , pp. 141-150
    • Christianson, D.W.1
  • 117
    • 3242785011 scopus 로고    scopus 로고
    • Isoprenoids: Remarkable Diversity of Form and Function
    • Holstein, S. A.; Hohl, R. J. Isoprenoids: Remarkable Diversity of Form and Function Lipids 2004, 39, 293-309 10.1007/s11745-004-1233-3
    • (2004) Lipids , vol.39 , pp. 293-309
    • Holstein, S.A.1    Hohl, R.J.2
  • 118
    • 0002503177 scopus 로고    scopus 로고
    • Bile Acids as Building Blocks of Supramolecular Hosts
    • Tamminen, J.; Kolehmainen, E. Bile Acids as Building Blocks of Supramolecular Hosts Molecules 2001, 6, 21-46 10.3390/60100021
    • (2001) Molecules , vol.6 , pp. 21-46
    • Tamminen, J.1    Kolehmainen, E.2
  • 120
    • 39149133975 scopus 로고    scopus 로고
    • Bile Acids as Building Blocks of Amphiphilic Polymers. Applications and Comparison with Other Systems
    • Durand, A. Bile Acids as Building Blocks of Amphiphilic Polymers. Applications and Comparison with Other Systems Collect. Czech. Chem. Commun. 2007, 72, 1553-1578 10.1135/cccc20071553
    • (2007) Collect. Czech. Chem. Commun. , vol.72 , pp. 1553-1578
    • Durand, A.1
  • 121
    • 14844358214 scopus 로고    scopus 로고
    • Bile Acid Derivatives as Enantiodifferentiating Host Molecules in Inclusion Processes
    • Bortolini, O.; Fantin, G.; Fogagnolo, M. Bile Acid Derivatives as Enantiodifferentiating Host Molecules in Inclusion Processes Chirality 2005, 17, 121-130 10.1002/chir.20126
    • (2005) Chirality , vol.17 , pp. 121-130
    • Bortolini, O.1    Fantin, G.2    Fogagnolo, M.3
  • 122
    • 50249180215 scopus 로고    scopus 로고
    • Bile Acids: Chemistry, Pathochemistry, Biology, Pathobiology, and Therapeutics
    • Hofmann, A. F.; Hagey, L. R. Bile Acids: Chemistry, Pathochemistry, Biology, Pathobiology, and Therapeutics Cell. Mol. Life Sci. 2008, 65, 2461-2483 10.1007/s00018-008-7568-6
    • (2008) Cell. Mol. Life Sci. , vol.65 , pp. 2461-2483
    • Hofmann, A.F.1    Hagey, L.R.2
  • 123
    • 0002148515 scopus 로고    scopus 로고
    • Bile Acids in Drug Discovery
    • Enhsen, A.; Kramer, W.; Wess, G. Bile Acids in Drug Discovery Drug Discovery Today 1998, 3, 409-418 10.1016/S1359-6446(96)10046-5
    • (1998) Drug Discovery Today , vol.3 , pp. 409-418
    • Enhsen, A.1    Kramer, W.2    Wess, G.3
  • 124
    • 34548458522 scopus 로고    scopus 로고
    • Exploitation of Bile Acid Transport Systems in Prodrug Design
    • Sievänen, E. Exploitation of Bile Acid Transport Systems in Prodrug Design Molecules 2007, 12, 1859-1889 10.3390/12081859
    • (2007) Molecules , vol.12 , pp. 1859-1889
    • Sievänen, E.1
  • 125
    • 77950808392 scopus 로고    scopus 로고
    • Bile Acids in Asymmetric Synthesis and Chiral Discrimination
    • Bortolini, O.; Fantin, G.; Fogagnolo, M. Bile Acids in Asymmetric Synthesis and Chiral Discrimination Chirality 2010, 22, 486-494 10.1002/chir.20769
    • (2010) Chirality , vol.22 , pp. 486-494
    • Bortolini, O.1    Fantin, G.2    Fogagnolo, M.3
  • 126
    • 84901281300 scopus 로고    scopus 로고
    • Synthesis and Evaluation of (18)F-Labeled Bile Acid Compound: A Potential PET Imaging Agent for FXR Related Diseases
    • Jia, L.; Jiang, D.; Hu, P.; Li, X.; Shi, H.; Cheng, D.; Zhang, L. Synthesis and Evaluation of (18)F-Labeled Bile Acid Compound: a Potential PET Imaging Agent for FXR Related Diseases Nucl. Med. Biol. 2014, 41, 495-500 10.1016/j.nucmedbio.2014.03.016
    • (2014) Nucl. Med. Biol. , vol.41 , pp. 495-500
    • Jia, L.1    Jiang, D.2    Hu, P.3    Li, X.4    Shi, H.5    Cheng, D.6    Zhang, L.7
  • 127
    • 24744463110 scopus 로고    scopus 로고
    • Synthesis of Bile Acid Dimers Linked with 1,2,3-Triazole Ring at C-3, C-11, and C-24 Positions
    • Aher, N. G.; Pore, V. S. Synthesis of Bile Acid Dimers Linked with 1,2,3-Triazole Ring at C-3, C-11, and C-24 Positions Synlett 2005, 14, 2155-2158 10.1055/s-2005-872223
    • (2005) Synlett , vol.14 , pp. 2155-2158
    • Aher, N.G.1    Pore, V.S.2
  • 128
    • 36148937894 scopus 로고    scopus 로고
    • Design, Synthesis, and Micellar Properties of Bile Acid Dimers and Oligomers Linked with a 1,2,3-Triazole Ring
    • Aher, N. G.; Pore, V. S.; Patil, S. P. Design, Synthesis, and Micellar Properties of Bile Acid Dimers and Oligomers Linked with a 1,2,3-Triazole Ring Tetrahedron 2007, 63, 12927-12934 10.1016/j.tet.2007.10.042
    • (2007) Tetrahedron , vol.63 , pp. 12927-12934
    • Aher, N.G.1    Pore, V.S.2    Patil, S.P.3
  • 129
    • 38149133668 scopus 로고    scopus 로고
    • Synthesis of 1,2,3-Triazole-containing Bile Acid Dimers and Properties of Inverse Micellar Mimic
    • Zhang, Z.; Ju, Y.; Zhao, Y. Synthesis of 1,2,3-Triazole-containing Bile Acid Dimers and Properties of Inverse Micellar Mimic Chem. Lett. 2007, 36, 1450-1451 10.1246/cl.2007.1450
    • (2007) Chem. Lett. , vol.36 , pp. 1450-1451
    • Zhang, Z.1    Ju, Y.2    Zhao, Y.3
  • 130
    • 84939417956 scopus 로고    scopus 로고
    • Synthesis of Isomeric Dimers of Deoxycholic Acid Derivatives Linked by 1,2,3-Triazole
    • Madrzak-Litwa, I.; Wojciechowska, A.; Paryzek, Z. Synthesis of Isomeric Dimers of Deoxycholic Acid Derivatives Linked by 1,2,3-Triazole Synth. Commun. 2015, 45, 1222-1230 10.1080/00397911.2015.1014116
    • (2015) Synth. Commun. , vol.45 , pp. 1222-1230
    • Madrzak-Litwa, I.1    Wojciechowska, A.2    Paryzek, Z.3
  • 131
    • 84894427282 scopus 로고    scopus 로고
    • Tripodal Bile Acid Architectures Based on a Triarylphosphine Oxide Core Obtained by Copper-Catalysed (1,3)-Dipolar Cycloaddition: Synthesis and Preliminary Aggregation Studies
    • Thota, B. N. S.; Savyasachi, A. J.; Lukashev, N.; Beletskaya, I.; Maitra, U. Tripodal Bile Acid Architectures Based on a Triarylphosphine Oxide Core Obtained by Copper-Catalysed (1,3)-Dipolar Cycloaddition: Synthesis and Preliminary Aggregation Studies Eur. J. Org. Chem. 2014, 2014, 1406-1415 10.1002/ejoc.201301443
    • (2014) Eur. J. Org. Chem. , vol.2014 , pp. 1406-1415
    • Thota, B.N.S.1    Savyasachi, A.J.2    Lukashev, N.3    Beletskaya, I.4    Maitra, U.5
  • 132
    • 77149169413 scopus 로고    scopus 로고
    • Molecular Pockets Derived from Cholic Acid as Chemosensors for Metal Ions
    • Zhang, J.; Luo, J.; Zhu, X. X.; Junk, M. J. N.; Hinderberger, D. Molecular Pockets Derived from Cholic Acid as Chemosensors for Metal Ions Langmuir 2010, 26, 2958-2962 10.1021/la9028996
    • (2010) Langmuir , vol.26 , pp. 2958-2962
    • Zhang, J.1    Luo, J.2    Zhu, X.X.3    Junk, M.J.N.4    Hinderberger, D.5
  • 133
    • 69249223458 scopus 로고    scopus 로고
    • 2+ Ion and Their Logic Gate Behaviour
    • 2+Ion and Their Logic Gate Behaviour Tetrahedron Lett. 2009, 50, 5842-5845 10.1016/j.tetlet.2009.08.007
    • (2009) Tetrahedron Lett. , vol.50 , pp. 5842-5845
    • Kumar, A.1    Pandey, P.S.2
  • 134
    • 80054744508 scopus 로고    scopus 로고
    • Oligocholate Foldamers as Carriers for Hydrophilic Molecules Across Lipid Bilayers
    • Zhang, S.; Zhao, Y. Oligocholate Foldamers as Carriers for Hydrophilic Molecules Across Lipid Bilayers Chem.-Eur. J. 2011, 17, 12444-12451 10.1002/chem.201101510
    • (2011) Chem. - Eur. J. , vol.17 , pp. 12444-12451
    • Zhang, S.1    Zhao, Y.2
  • 135
    • 73949096670 scopus 로고    scopus 로고
    • Synthesis of Click Bile Acid Polymers and Their Application in Stabilization of Silver Nanoparticles Showing Iodide Sensing Property
    • Kumar, A.; Chhatra, R. K.; Pandey, P. S. Synthesis of Click Bile Acid Polymers and Their Application in Stabilization of Silver Nanoparticles Showing Iodide Sensing Property Org. Lett. 2010, 12, 24-27 10.1021/ol902351g
    • (2010) Org. Lett. , vol.12 , pp. 24-27
    • Kumar, A.1    Chhatra, R.K.2    Pandey, P.S.3
  • 136
    • 84868700776 scopus 로고    scopus 로고
    • Triazole-linked Polyamides and Polyesters Derived from Cholic Acid
    • Ivanysenko, O.; Strandman, S.; Zhu, X. X. Triazole-linked Polyamides and Polyesters Derived from Cholic Acid Polym. Chem. 2012, 3, 1962-1965 10.1039/c2py20168b
    • (2012) Polym. Chem. , vol.3 , pp. 1962-1965
    • Ivanysenko, O.1    Strandman, S.2    Zhu, X.X.3
  • 137
    • 69749086213 scopus 로고    scopus 로고
    • Copper-Catalyzed (1,3)-Dipolar Cycloaddition for the Synthesis of Macrocycles Containing Acyclic, Aromatic and Steroidal Moieties
    • Latyshev, G. V.; Baranov, M. S.; Kazantsev, A. V.; Averin, A. D.; Lukashev, N. V.; Beletskaya, I. P. Copper-Catalyzed (1,3)-Dipolar Cycloaddition for the Synthesis of Macrocycles Containing Acyclic, Aromatic and Steroidal Moieties Synthesis 2009, 2009, 2605-2615 10.1055/s-0029-1217400
    • (2009) Synthesis , vol.2009 , pp. 2605-2615
    • Latyshev, G.V.1    Baranov, M.S.2    Kazantsev, A.V.3    Averin, A.D.4    Lukashev, N.V.5    Beletskaya, I.P.6
  • 138
    • 80055084220 scopus 로고    scopus 로고
    • Synthesis of a Bile Acid-Based Click-Macrocycle and Its Application in Selective Recognition of Chloride Ion
    • Chhatra, R. K.; Kumar, A.; Pandey, P. S. Synthesis of a Bile Acid-Based Click-Macrocycle and Its Application in Selective Recognition of Chloride Ion J. Org. Chem. 2011, 76, 9086-9089 10.1021/jo201161n
    • (2011) J. Org. Chem. , vol.76 , pp. 9086-9089
    • Chhatra, R.K.1    Kumar, A.2    Pandey, P.S.3
  • 139
    • 38749094503 scopus 로고    scopus 로고
    • Anion Recognition by 1,2,3-Triazolium Receptors:Application of Click Chemistry in Anion Recognition
    • Kumar, A.; Pandey, P. S. Anion Recognition by 1,2,3-Triazolium Receptors:Application of Click Chemistry in Anion Recognition Org. Lett. 2008, 10, 165-168 10.1021/ol702457w
    • (2008) Org. Lett. , vol.10 , pp. 165-168
    • Kumar, A.1    Pandey, P.S.2
  • 140
    • 84891762733 scopus 로고    scopus 로고
    • A Click Chemistry Approach to Secosteroidal Macrocycles
    • Ibrahim-Ouali, M.; Hamze, K. A Click Chemistry Approach to Secosteroidal Macrocycles Steroids 2014, 80, 102-110 10.1016/j.steroids.2013.12.002
    • (2014) Steroids , vol.80 , pp. 102-110
    • Ibrahim-Ouali, M.1    Hamze, K.2
  • 142
    • 84555189821 scopus 로고    scopus 로고
    • Shortcut Access to Peptidosteroid Conjugates: Building Blocks for Solid-phase Bile Acid Scaffold Decoration by Convergent Ligation
    • Verzele, D.; Figaroli, S.; Madder, A. Shortcut Access to Peptidosteroid Conjugates: Building Blocks for Solid-phase Bile Acid Scaffold Decoration by Convergent Ligation Molecules 2011, 16, 10168-10186 10.3390/molecules161210168
    • (2011) Molecules , vol.16 , pp. 10168-10186
    • Verzele, D.1    Figaroli, S.2    Madder, A.3
  • 143
    • 33749986728 scopus 로고    scopus 로고
    • Design and Synthesis of Fluconazole/bile acid Conjugate Using Click Reaction
    • Pore, V. S.; Aher, N. G.; Kumar, M.; Shukla, P. K. Design and Synthesis of Fluconazole/bile acid Conjugate Using Click Reaction Tetrahedron 2006, 62, 11178-11186 10.1016/j.tet.2006.09.021
    • (2006) Tetrahedron , vol.62 , pp. 11178-11186
    • Pore, V.S.1    Aher, N.G.2    Kumar, M.3    Shukla, P.K.4
  • 145
    • 40749106101 scopus 로고    scopus 로고
    • Synthesis and Antimicrobial Activity of β-Lactam-bile Acid Conjugates Linked via Triazole
    • Vatmurge, N. S.; Hazra, B. G.; Pore, V. S.; Shirazi, F.; Chavan, P. S.; Deshpande, M. V. Synthesis and Antimicrobial Activity of β-Lactam-bile Acid Conjugates Linked via Triazole Bioorg. Med. Chem. Lett. 2008, 18, 2043-2047 10.1016/j.bmcl.2008.01.102
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 2043-2047
    • Vatmurge, N.S.1    Hazra, B.G.2    Pore, V.S.3    Shirazi, F.4    Chavan, P.S.5    Deshpande, M.V.6
  • 146
    • 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 10.1039/c0ob01188f
    • (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
  • 147
    • 84903318522 scopus 로고    scopus 로고
    • Azidoisocyanides, New Bifunctional Reagents for Multicomponent Reactions and Biomolecule Modifications
    • Sokolova, N. V.; Nenajdenko, V. G. Azidoisocyanides, New Bifunctional Reagents for Multicomponent Reactions and Biomolecule Modifications Chem. Nat. Compd. 2014, 50, 197-213 10.1007/s10600-014-0914-z
    • (2014) Chem. Nat. Compd. , vol.50 , pp. 197-213
    • Sokolova, N.V.1    Nenajdenko, V.G.2
  • 149
    • 84916214199 scopus 로고    scopus 로고
    • Man-Made Cytotoxic Steroids: Exemplary Agents for Cancer Therapy
    • Bansal, R.; Acharya, P. C. Man-Made Cytotoxic Steroids: Exemplary Agents for Cancer Therapy Chem. Rev. 2014, 114, 6986-7005 10.1021/cr4002935
    • (2014) Chem. Rev. , vol.114 , pp. 6986-7005
    • Bansal, R.1    Acharya, P.C.2
  • 150
    • 84892821933 scopus 로고    scopus 로고
    • Synthesis of Steroidal Dendrimers Modified by "Click" Chemistry with PAMAM Dendrons as Unimolecular Micelles
    • Soto-Castro, D.; Magana-Vergara, N. E.; Farfán, N.; Santillan, R. Synthesis of Steroidal Dendrimers Modified by "Click" Chemistry with PAMAM Dendrons as Unimolecular Micelles Tetrahedron Lett. 2014, 55, 1014-1019 10.1016/j.tetlet.2013.12.066
    • (2014) Tetrahedron Lett. , vol.55 , pp. 1014-1019
    • Soto-Castro, D.1    Magana-Vergara, N.E.2    Farfán, N.3    Santillan, R.4
  • 151
    • 84857031226 scopus 로고    scopus 로고
    • A Facile "Click" Approach to Novel 15β-Triazolyl-5α-androstane Derivatives, and an Evaluation of Their Antiproliferative Activities in vitro
    • Kádár, Z.; Molnár, J.; Schneider, G.; Zupkó, I.; Frank, E. A Facile "Click" Approach to Novel 15β-Triazolyl-5α-androstane Derivatives, and an Evaluation of Their Antiproliferative Activities in vitro Bioorg. Med. Chem. 2012, 20, 1396-1402 10.1016/j.bmc.2012.01.008
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 1396-1402
    • Kádár, Z.1    Molnár, J.2    Schneider, G.3    Zupkó, I.4    Frank, E.5
  • 152
    • 79960445267 scopus 로고    scopus 로고
    • Synthesis of Novel Steroidal 17α-Triazolyl Derivatives via Cu(I)-catalyzed Azide-alkyne Cycloaddition, and an Evaluation of Their Cytotoxic Activity in vitro
    • Frank, E.; Molnár, J.; Zupkó, I.; Kádár, Z.; Wölfling, J. Synthesis of Novel Steroidal 17α-Triazolyl Derivatives via Cu(I)-catalyzed Azide-alkyne Cycloaddition, and an Evaluation of Their Cytotoxic Activity in vitro Steroids 2011, 76, 1141-1148 10.1016/j.steroids.2011.05.002
    • (2011) Steroids , vol.76 , pp. 1141-1148
    • Frank, E.1    Molnár, J.2    Zupkó, I.3    Kádár, Z.4    Wölfling, J.5
  • 153
    • 81255128918 scopus 로고    scopus 로고
    • Efficient Approach to Novel 1α-Triazolyl-5α-androstane Derivatives as Potent Antiproliferative Agents
    • Kádár, Z.; Baji, A.; Zupkó, I.; Bartók, T.; Wölfling, J.; Frank, E. Efficient Approach to Novel 1α-Triazolyl-5α-androstane Derivatives as Potent Antiproliferative Agents Org. Biomol. Chem. 2011, 9, 8051-8057 10.1039/c1ob06086d
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 8051-8057
    • Kádár, Z.1    Baji, A.2    Zupkó, I.3    Bartók, T.4    Wölfling, J.5    Frank, E.6
  • 154
    • 79959627028 scopus 로고    scopus 로고
    • Synthesis and in vitro Antiproliferative Activity of Novel Androst-5-ene Triazolyl and Tetrazolyl Derivatives
    • Kádár, Z.; Kovács, D.; Frank, E.; Schneider, G.; Huber, J.; Zupkó, I.; Bartók, T.; Wölfling, J. Synthesis and in vitro Antiproliferative Activity of Novel Androst-5-ene Triazolyl and Tetrazolyl Derivatives Molecules 2011, 16, 4786-4806 10.3390/molecules16064786
    • (2011) Molecules , vol.16 , pp. 4786-4806
    • Kádár, Z.1    Kovács, D.2    Frank, E.3    Schneider, G.4    Huber, J.5    Zupkó, I.6    Bartók, T.7    Wölfling, J.8
  • 155
    • 77955926541 scopus 로고    scopus 로고
    • D-ring Substituted 1,2,3-Triazolyl 20-Keto Pregnenanes as Potential Anticancer Agents: Synthesis and Biological Evaluation
    • Banday, A. H.; Shameem, S. A.; Gupta, B. D.; Kumar, H. M. S. D-ring Substituted 1,2,3-Triazolyl 20-Keto Pregnenanes as Potential Anticancer Agents: Synthesis and Biological Evaluation Steroids 2010, 75, 801-804 10.1016/j.steroids.2010.02.015
    • (2010) Steroids , vol.75 , pp. 801-804
    • Banday, A.H.1    Shameem, S.A.2    Gupta, B.D.3    Kumar, H.M.S.4
  • 156
    • 84888120103 scopus 로고    scopus 로고
    • Click Chemistry Decoration of Amino Sterols as Promising Strategy to Developed New Leishmanicidal Drugs
    • Porta, E. O. J.; Carvalho, P. B.; Avery, M. A.; Tekwani, B. L.; Labadie, G. R. Click Chemistry Decoration of Amino Sterols as Promising Strategy to Developed New Leishmanicidal Drugs Steroids 2014, 79, 28-36 10.1016/j.steroids.2013.10.010
    • (2014) Steroids , vol.79 , pp. 28-36
    • Porta, E.O.J.1    Carvalho, P.B.2    Avery, M.A.3    Tekwani, B.L.4    Labadie, G.R.5
  • 157
    • 84900831753 scopus 로고    scopus 로고
    • Synthesis of Novel 1,2,3-Triazolyl Derivatives of Pregnane, Androstane and D-Homoandrostane. Tandem "Click" Reaction/Cu-catalyzed D-Homo Rearrangement
    • Kotovshchikov, Y. N.; Latyshev, G. V.; Lukashev, N. V.; Beletskaya, I. P. Synthesis of Novel 1,2,3-Triazolyl Derivatives of Pregnane, Androstane and D-Homoandrostane. Tandem "Click" Reaction/Cu-catalyzed D-Homo Rearrangement Org. Biomol. Chem. 2014, 12, 3707-3720 10.1039/C4OB00404C
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 3707-3720
    • Kotovshchikov, Y.N.1    Latyshev, G.V.2    Lukashev, N.V.3    Beletskaya, I.P.4
  • 158
    • 78049472036 scopus 로고    scopus 로고
    • Preparation and Preliminary Bioevaluation of 99mTc(CO)3-11β-Progesterone Derivative Prepared via Click Chemistry Route
    • Dhyani, M. V.; Satpati, D.; Korde, A.; Dev Sarma, H.; Kumar, Ch.; Banerjee, S. Preparation and Preliminary Bioevaluation of 99mTc(CO)3-11β-Progesterone Derivative Prepared via Click Chemistry Route Nucl. Med. Biol. 2010, 37, 997-1004 10.1016/j.nucmedbio.2010.05.005
    • (2010) Nucl. Med. Biol. , vol.37 , pp. 997-1004
    • Dhyani, M.V.1    Satpati, D.2    Korde, A.3    Dev Sarma, H.4    Kumar, Ch.5    Banerjee, S.6
  • 159
    • 80054694552 scopus 로고    scopus 로고
    • Synthesis and Preliminary Bioevaluation of 99mTc(CO)3-17a-Triazolylandrost-4-ene-3-one Derivative Prepared via Click Chemistry Route
    • Dhyani, M. V.; Satpati, D.; Korde, A.; Banerjee, S. Synthesis and Preliminary Bioevaluation of 99mTc(CO)3-17a-Triazolylandrost-4-ene-3-one Derivative Prepared via Click Chemistry Route Cancer Biother.Radiopharm. 2011, 26, 539-545 10.1089/cbr.2011.0966
    • (2011) Cancer Biother.Radiopharm. , vol.26 , pp. 539-545
    • Dhyani, M.V.1    Satpati, D.2    Korde, A.3    Banerjee, S.4
  • 160
    • 84861199309 scopus 로고    scopus 로고
    • Synthesis of Ferrocene-labeled Steroids via Copper-catalyzed Azide-alkyne Cycloaddition. Reactivity Difference between 2β-, 6β- and 16β-Azido-androstanes
    • Féher, K.; Balogh, J.; Csók, Z.; Kégl, T.; Kollár, L.; Skoda-Földes, R. Synthesis of Ferrocene-labeled Steroids via Copper-catalyzed Azide-alkyne Cycloaddition. Reactivity Difference Between 2β-, 6β- and 16β-Azido-androstanes Steroids 2012, 77, 738-744 10.1016/j.steroids.2012.04.005
    • (2012) Steroids , vol.77 , pp. 738-744
    • Féher, K.1    Balogh, J.2    Csók, Z.3    Kégl, T.4    Kollár, L.5    Skoda-Földes, R.6
  • 162
    • 84873049158 scopus 로고    scopus 로고
    • Preparation, Preliminary Screening of New Types of Steroid Conjugates and Their Activities on Steroid Receptors
    • Jurášek, M.; Džubák, P.; Sedlák, D.; Dvořáková, H.; Hajdúch, M.; Bartuněk, P.; Drašar, P. Preparation, Preliminary Screening of New Types of Steroid Conjugates and Their Activities on Steroid Receptors Steroids 2013, 78, 356-361 10.1016/j.steroids.2012.11.016
    • (2013) Steroids , vol.78 , pp. 356-361
    • Jurášek, M.1    Džubák, P.2    Sedlák, D.3    Dvořáková, H.4    Hajdúch, M.5    Bartuněk, P.6    Drašar, P.7
  • 164
    • 84866077273 scopus 로고    scopus 로고
    • 17α-Ethynylestradiol Peptide Labeling by "Click" Chemistry
    • Bol'shakov, O. I.; Lebedyeva, I. O.; Katritzky, A. R. 17α-Ethynylestradiol Peptide Labeling by "Click" Chemistry Synthesis 2012, 44, 2926-2932 10.1055/s-0032-1316702
    • (2012) Synthesis , vol.44 , pp. 2926-2932
    • Bol'Shakov, O.I.1    Lebedyeva, I.O.2    Katritzky, A.R.3
  • 165
    • 85027928389 scopus 로고    scopus 로고
    • Synthesis of Peptide Conjugates of Mestranol by a 1,3-Dipolar Cycloaddition Click Reaction
    • Sokolova, N. V.; Nenajdenko, V. G. Synthesis of Peptide Conjugates of Mestranol by a 1,3-Dipolar Cycloaddition Click Reaction Chem. Heterocycl. Compd. 2012, 48, 903-906 10.1007/s10593-012-1074-3
    • (2012) Chem. Heterocycl. Compd. , vol.48 , pp. 903-906
    • Sokolova, N.V.1    Nenajdenko, V.G.2
  • 166
    • 84898847679 scopus 로고    scopus 로고
    • I-catalyzed Alkyne-azide Cycloaddition as Direct Conjugation/cyclization Method of Peptides to Steroids
    • I-catalyzed Alkyne-azide Cycloaddition as Direct Conjugation/cyclization Method of Peptides to Steroids Tetrahedron 2014, 70, 3297-3305 10.1016/j.tet.2013.10.032
    • (2014) Tetrahedron , vol.70 , pp. 3297-3305
    • Echemendia, R.1    Concepción, O.2    Morales, F.E.3    Paixa'o, M.W.4    Rivera, D.G.5
  • 167
    • 84890957694 scopus 로고    scopus 로고
    • Click Chemistry Inspired Highly Facile Synthesis of Triazolyl Ethisterone Glycoconjugates
    • Kumar, D.; Mishra, K. B.; Mishra, B. B.; Mondal, S.; Tiwari, V. K. Click Chemistry Inspired Highly Facile Synthesis of Triazolyl Ethisterone Glycoconjugates Steroids 2014, 80, 71-79 10.1016/j.steroids.2013.11.022
    • (2014) Steroids , vol.80 , pp. 71-79
    • Kumar, D.1    Mishra, K.B.2    Mishra, B.B.3    Mondal, S.4    Tiwari, V.K.5
  • 168
    • 49449098341 scopus 로고    scopus 로고
    • Lipid-conjugated Oligonucleotides via "Click Chemistry" Efficiently Inhibit Hepatitis C Virus Translation
    • Godeau, G.; Staedel, C.; Barthélémy, P. Lipid-conjugated Oligonucleotides via "Click Chemistry" Efficiently Inhibit Hepatitis C Virus Translation J. Med. Chem. 2008, 51, 4374-4376 10.1021/jm800518u
    • (2008) J. Med. Chem. , vol.51 , pp. 4374-4376
    • Godeau, G.1    Staedel, C.2    Barthélémy, P.3
  • 169
    • 53549099104 scopus 로고    scopus 로고
    • Synthesis of a Side Chain Liquid Crystalline Polymer Containing the Cholesteryl Moiety via ROP and "Click" Chemistry
    • Cui, Z.; Zhang, Y.; He, S. Synthesis of a Side Chain Liquid Crystalline Polymer Containing the Cholesteryl Moiety via ROP and "Click" Chemistry Colloid Polym. Sci. 2008, 286, 1553-1559 10.1007/s00396-008-1916-9
    • (2008) Colloid Polym. Sci. , vol.286 , pp. 1553-1559
    • Cui, Z.1    Zhang, Y.2    He, S.3
  • 170
    • 77954610087 scopus 로고    scopus 로고
    • Synthesis and Characterization of Novel Cholesterol Based Mesogenic Compounds Using "Click" Chemistry
    • Majumdar, K. C.; Mondal, S.; Sinha, R. K. Synthesis and Characterization of Novel Cholesterol Based Mesogenic Compounds Using "Click" Chemistry New J. Chem. 2010, 34, 1255-1260 10.1039/b9nj00744j
    • (2010) New J. Chem. , vol.34 , pp. 1255-1260
    • Majumdar, K.C.1    Mondal, S.2    Sinha, R.K.3
  • 171
    • 84873808770 scopus 로고    scopus 로고
    • Synthesis and Characterization of Cholesterol-(1,2,3-triazole)-PEG via Click Chemistry
    • Xu, W.; Luo, B.; Li, C.; Yang, J.; Zhou, C. Synthesis and Characterization of Cholesterol-(1,2,3-triazole)-PEG via Click Chemistry Adv. Mater. Res. 2013, 647, 499-503 10.4028/www.scientific.net/AMR.647.499
    • (2013) Adv. Mater. Res. , vol.647 , pp. 499-503
    • Xu, W.1    Luo, B.2    Li, C.3    Yang, J.4    Zhou, C.5
  • 172
    • 84885173308 scopus 로고    scopus 로고
    • "Click" Synthesized Sterol-based Cationic Lipids as Gene Carriers, and the Effect of Skeletons and Headgroups on Gene Delivery
    • Sheng, R.; Luo, T.; Sun, J.; Wang, Z.; Cao, A.; Li, H. "Click" Synthesized Sterol-based Cationic Lipids as Gene Carriers, and the Effect of Skeletons and Headgroups on Gene Delivery Bioorg. Med. Chem. 2013, 21, 6366-6377 10.1016/j.bmc.2013.08.047
    • (2013) Bioorg. Med. Chem. , vol.21 , pp. 6366-6377
    • Sheng, R.1    Luo, T.2    Sun, J.3    Wang, Z.4    Cao, A.5    Li, H.6
  • 173
    • 84884194029 scopus 로고    scopus 로고
    • Efficient Synthesis of Novel A-Ring-substituted 1,2,3-Triazolylcholestane Derivatives via Catalytic Azide-alkyne Cycloaddition
    • Kádár, Z.; Frank, E.; Schneider, G.; Molnár, J.; Zupkó, I.; Kóti, J.; Schönecker, B.; Wölfling, J. Efficient Synthesis of Novel A-Ring-substituted 1,2,3-Triazolylcholestane Derivatives via Catalytic Azide-alkyne Cycloaddition Arkivoc 2012, iii, 279-296
    • (2012) Arkivoc , vol.3 , pp. 279-296
    • Kádár, Z.1    Frank, E.2    Schneider, G.3    Molnár, J.4    Zupkó, I.5    Kóti, J.6    Schönecker, B.7    Wölfling, J.8
  • 174
    • 84872769330 scopus 로고    scopus 로고
    • Ursane-type Pentacyclic Triterpenoids as Useful Platforms to Discover Anticancer Drugs
    • Salvador, J. A.; Moreira, V. M.; Gonçalves, B. M.; Leal, A. S.; Jing, Y. Ursane-type Pentacyclic Triterpenoids as Useful Platforms to Discover Anticancer Drugs Nat. Prod. Rep. 2012, 29, 1463-1479 10.1039/c2np20060k
    • (2012) Nat. Prod. Rep. , vol.29 , pp. 1463-1479
    • Salvador, J.A.1    Moreira, V.M.2    Gonçalves, B.M.3    Leal, A.S.4    Jing, Y.5
  • 175
    • 84867055462 scopus 로고    scopus 로고
    • Synthetic Oleanane Triterpenoids: Multifunctional Drugs with a Broad Range of Applications for Prevention and Treatment of Chronic Disease
    • Liby, K. T.; Sporn, M. B. Synthetic Oleanane Triterpenoids: Multifunctional Drugs with a Broad Range of Applications for Prevention and Treatment of Chronic Disease Pharmacol. Rev. 2012, 64, 972-1003 10.1124/pr.111.004846
    • (2012) Pharmacol. Rev. , vol.64 , pp. 972-1003
    • Liby, K.T.1    Sporn, M.B.2
  • 176
    • 73349109760 scopus 로고    scopus 로고
    • Triterpenoids as New Promising Anticancer Drugs
    • Petronelli, A.; Pannitteri, G.; Testa, U. Triterpenoids as New Promising Anticancer Drugs Anti-Cancer Drugs 2009, 20, 880-892 10.1097/CAD.0b013e328330fd90
    • (2009) Anti-Cancer Drugs , vol.20 , pp. 880-892
    • Petronelli, A.1    Pannitteri, G.2    Testa, U.3
  • 177
    • 70349525363 scopus 로고    scopus 로고
    • Plant-derived Triterpenoids and Analogues as Antitumor and Anti-HIV agents
    • Kuo, R.-Y.; Qian, K.; Morris-Natschke, S. L.; Lee, K.-H. Plant-derived Triterpenoids and Analogues as Antitumor and Anti-HIV agents Nat. Prod. Rep. 2009, 26, 1321-1344 10.1039/b810774m
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 1321-1344
    • Kuo, R.-Y.1    Qian, K.2    Morris-Natschke, S.L.3    Lee, K.-H.4
  • 178
    • 84964199238 scopus 로고    scopus 로고
    • Triterpenoids
    • See also other reviews of the authors published in this journal since 2001
    • Hill, R. A.; Connolly, J. D. Triterpenoids Nat. Prod. Rep. 2015, 32, 273-327 See also other reviews of the authors published in this journal since 2001. 10.1039/C4NP00101J
    • (2015) Nat. Prod. Rep. , vol.32 , pp. 273-327
    • Hill, R.A.1    Connolly, J.D.2
  • 179
    • 65249125749 scopus 로고    scopus 로고
    • Synthesis of Glucoconjugates of Oleanolic Acid as Inhibitors of Glycogen Phosphorylase
    • Cheng, K.; Liu, J.; Liu, X.; Li, H.; Sun, H.; Xie, J. Synthesis of Glucoconjugates of Oleanolic Acid as Inhibitors of Glycogen Phosphorylase Carbohydr. Res. 2009, 344, 841-850 10.1016/j.carres.2009.02.012
    • (2009) Carbohydr. Res. , vol.344 , pp. 841-850
    • Cheng, K.1    Liu, J.2    Liu, X.3    Li, H.4    Sun, H.5    Xie, J.6
  • 180
    • 77954615525 scopus 로고    scopus 로고
    • Tethered Derivatives of D-Glucose and Pentacyclic Triterpenes for Homo/heterobivalent Inhibition of Glycogen Phosphorylase
    • Cheng, K.; Liu, J.; Sun, H.; Bokor, E.; Czifrák, K.; Kónya, B.; Tóth, M.; Docsa, T.; Gergely, P.; Somsák, L. Tethered Derivatives of D-Glucose and Pentacyclic Triterpenes for Homo/heterobivalent Inhibition of Glycogen Phosphorylase New J. Chem. 2010, 34, 1450-1464 10.1039/b9nj00602h
    • (2010) New J. Chem. , vol.34 , pp. 1450-1464
    • Cheng, K.1    Liu, J.2    Sun, H.3    Bokor, E.4    Czifrák, K.5    Kónya, B.6    Tóth, M.7    Docsa, T.8    Gergely, P.9    Somsák, L.10
  • 181
    • 77949669520 scopus 로고    scopus 로고
    • Synthesis of Oleanolic Acid Dimers as Inhibitors of Glycogen Phosphorylase
    • Cheng, K.; Liu, J.; Sun, H.; Xie, J. Synthesis of Oleanolic Acid Dimers as Inhibitors of Glycogen Phosphorylase Chem. Biodiversity 2010, 7, 690-697 10.1002/cbdv.200900086
    • (2010) Chem. Biodiversity , vol.7 , pp. 690-697
    • Cheng, K.1    Liu, J.2    Sun, H.3    Xie, J.4
  • 182
    • 84879063655 scopus 로고    scopus 로고
    • Development of Oleanane-Type Triterpenes as a New Class of HCV Entry Inhibitors
    • Yu, F.; Wang, Q.; Zhang, Z.; Peng, Y.; Qiu, Y.; Shi, Y.; Zheng, Y.; Xiao, S.; Wang, H.; Huang, X. et al. Development of Oleanane-Type Triterpenes as a New Class of HCV Entry Inhibitors J. Med. Chem. 2013, 56, 4300-4319 10.1021/jm301910a
    • (2013) J. Med. Chem. , vol.56 , pp. 4300-4319
    • Yu, F.1    Wang, Q.2    Zhang, Z.3    Peng, Y.4    Qiu, Y.5    Shi, Y.6    Zheng, Y.7    Xiao, S.8    Wang, H.9    Huang, X.10
  • 184
    • 84880781906 scopus 로고    scopus 로고
    • 1,2,3-Triazole-Substituted Oleanolic Acid Derivatives: Synthesis and Antiproliferative Activity
    • Pertino, M. W.; Lopez, C.; Theoduloz, C.; Schmeda-Hirschmann, G. 1,2,3-Triazole-Substituted Oleanolic Acid Derivatives: Synthesis and Antiproliferative Activity Molecules 2013, 18, 7661-7674 10.3390/molecules18077661
    • (2013) Molecules , vol.18 , pp. 7661-7674
    • Pertino, M.W.1    Lopez, C.2    Theoduloz, C.3    Schmeda-Hirschmann, G.4
  • 185
    • 79960401541 scopus 로고    scopus 로고
    • Synthesis and Anion Recognition of a Novel Oleanolic Acid-based Cyclic Dimer
    • Hu, J.; Li, R.; Lu, J.; Ju, Y. Synthesis and Anion Recognition of a Novel Oleanolic Acid-based Cyclic Dimer Tetrahedron Lett. 2011, 52, 4211-4214 10.1016/j.tetlet.2011.06.022
    • (2011) Tetrahedron Lett. , vol.52 , pp. 4211-4214
    • Hu, J.1    Li, R.2    Lu, J.3    Ju, Y.4
  • 186
    • 76649106073 scopus 로고    scopus 로고
    • Betulinic Acid, a Natural Compound with Potent Anticancer Effects
    • Mullauer, F. B.; Kessler, J. H.; Medema, J. P. Betulinic Acid, a Natural Compound with Potent Anticancer Effects Anti-Cancer Drugs 2010, 21, 215-227 10.1097/CAD.0b013e3283357c62
    • (2010) Anti-Cancer Drugs , vol.21 , pp. 215-227
    • Mullauer, F.B.1    Kessler, J.H.2    Medema, J.P.3
  • 188
    • 33747802067 scopus 로고    scopus 로고
    • Pharmacological Properties of the Ubiquitous Natural Product Betulin
    • Alakurtti, S.; Mäkelä, T.; Koskimies, S.; Yli-Kauhaluoma, J. Pharmacological Properties of the Ubiquitous Natural Product Betulin Eur. J. Pharm. Sci. 2006, 29, 1-13 10.1016/j.ejps.2006.04.006
    • (2006) Eur. J. Pharm. Sci. , vol.29 , pp. 1-13
    • Alakurtti, S.1    Mäkelä, T.2    Koskimies, S.3    Yli-Kauhaluoma, J.4
  • 189
    • 84862784033 scopus 로고    scopus 로고
    • Anti-AIDS Agents 88. Anti-HIV Conjugates of Betulin and Betulinic Acid with AZT Prepared via Click Chemistry
    • Bori, I. D.; Hung, H.-Y.; Qian, K.; Chen, C.-H.; Morris-Natschke, S. L.; Lee, K.-H. Anti-AIDS Agents 88. Anti-HIV Conjugates of Betulin and Betulinic Acid with AZT Prepared via Click Chemistry Tetrahedron Lett. 2012, 53, 1987-1989 10.1016/j.tetlet.2012.02.022
    • (2012) Tetrahedron Lett. , vol.53 , pp. 1987-1989
    • Bori, I.D.1    Hung, H.-Y.2    Qian, K.3    Chen, C.-H.4    Morris-Natschke, S.L.5    Lee, K.-H.6
  • 190
    • 84907225755 scopus 로고    scopus 로고
    • Conjugation of a Nonspecific Antiviral Sapogenin with a Specific HIV Fusion Inhibitor: A Promising Strategy for Discovering New Antiviral Therapeutics
    • Wang, C.; Lu, L.; Na, H.; Li, X.; Wang, Q.; Jiang, X.; Xu, X.; Yu, F.; Zhang, T.; Li, J. et al. Conjugation of a Nonspecific Antiviral Sapogenin with a Specific HIV Fusion Inhibitor: A Promising Strategy for Discovering New Antiviral Therapeutics J. Med. Chem. 2014, 57, 7342-7354 10.1021/jm500763m
    • (2014) J. Med. Chem. , vol.57 , pp. 7342-7354
    • Wang, C.1    Lu, L.2    Na, H.3    Li, X.4    Wang, Q.5    Jiang, X.6    Xu, X.7    Yu, F.8    Zhang, T.9    Li, J.10
  • 195
    • 79959766022 scopus 로고    scopus 로고
    • 3 Molecule with Three Glycyrrhetinic Acid Units and Self-Assembly Properties
    • 3Molecule with Three Glycyrrhetinic Acid Units and Self-Assembly Properties Chin. J. Chem. 2011, 29, 1139-1142 10.1002/cjoc.201190213
    • (2011) Chin. J. Chem. , vol.29 , pp. 1139-1142
    • Hu, J.1    Yu, L.2    Zhang, M.3    Ju, Y.J.4
  • 197
    • 84869082314 scopus 로고    scopus 로고
    • A Dual-responsive Macrocycle Based on Glycyrrhetinic acid
    • Hu, J.; Wu, J.; Lu, J.; Ju, Y. A Dual-responsive Macrocycle Based on Glycyrrhetinic acid Tetrahedron Lett. 2012, 53, 6705-6709 10.1016/j.tetlet.2012.09.118
    • (2012) Tetrahedron Lett. , vol.53 , pp. 6705-6709
    • Hu, J.1    Wu, J.2    Lu, J.3    Ju, Y.4
  • 198
    • 84905905997 scopus 로고    scopus 로고
    • Synthesis and Evaluation of Triazole Linked Glycosylated 18β-Glycyrrhetinic Acid Derivatives as Anticancer Agents
    • Parida, P. K.; Sau, A.; Ghosh, T.; Jana, K.; Biswas, K.; Raha, S.; Misra, A. K. Synthesis and Evaluation of Triazole Linked Glycosylated 18β-Glycyrrhetinic Acid Derivatives as Anticancer Agents Bioorg. Med. Chem. Lett. 2014, 24, 3865-3868 10.1016/j.bmcl.2014.06.054
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 3865-3868
    • Parida, P.K.1    Sau, A.2    Ghosh, T.3    Jana, K.4    Biswas, K.5    Raha, S.6    Misra, A.K.7
  • 199
    • 84866913755 scopus 로고    scopus 로고
    • 2-Adrenergic Receptor-Gs Signaling by Changing the Location of Gαs in Lipid Rafts
    • 2-Adrenergic Receptor-Gs Signaling by Changing the Location of Gαs in Lipid Rafts PLoS One 2012, 7 e44921 10.1371/journal.pone.0044921
    • (2012) PLoS One , vol.7 , pp. e44921
    • Shi, Q.1    Hou, Y.2    Hou, J.3    Pan, P.4    Liu, Z.5    Jiang, M.6    Gao, J.7    Bai, G.8
  • 200
    • 84893489417 scopus 로고    scopus 로고
    • A Novel Approach for Fluorescent Visualization of Glycyrrhetic Acid on a Cell with a Quantum Dot
    • Hou, J.; Shi, Q.; Cao, M.; Pan, P.; Ge, G.; Fan, X.; Bai, G.; Xin, Y. A Novel Approach for Fluorescent Visualization of Glycyrrhetic Acid on a Cell with a Quantum Dot Biochemistry (Moscow) 2014, 79, 25-30 10.1134/S0006297914010040
    • (2014) Biochemistry (Moscow) , vol.79 , pp. 25-30
    • Hou, J.1    Shi, Q.2    Cao, M.3    Pan, P.4    Ge, G.5    Fan, X.6    Bai, G.7    Xin, Y.8
  • 201
    • 79952900480 scopus 로고    scopus 로고
    • Molecular Activities, Biosynthesis and Evolution of Triterpenoid Saponins
    • Augustin, J. M.; Kuzina, V.; Andersen, S. B.; Bak, S. Molecular Activities, Biosynthesis and Evolution of Triterpenoid Saponins Phytochemistry 2011, 72, 435-457 10.1016/j.phytochem.2011.01.015
    • (2011) Phytochemistry , vol.72 , pp. 435-457
    • Augustin, J.M.1    Kuzina, V.2    Andersen, S.B.3    Bak, S.4
  • 203
    • 84873739522 scopus 로고    scopus 로고
    • Synthesis and Conformational Study of Triazole-linked bis-Spirostanic Conjugates
    • Pérez-Labrada, K.; Morera, C.; Brouard, I.; Llerena, R.; Rivera, D. G. Synthesis and Conformational Study of Triazole-linked bis-Spirostanic Conjugates Tetrahedron Lett. 2013, 54, 1602-1606 10.1016/j.tetlet.2013.01.058
    • (2013) Tetrahedron Lett. , vol.54 , pp. 1602-1606
    • Pérez-Labrada, K.1    Morera, C.2    Brouard, I.3    Llerena, R.4    Rivera, D.G.5
  • 204
    • 82955237594 scopus 로고    scopus 로고
    • Click Chemistry: An Efficient Synthesis of Heterocycles Substituted with Steroids, Saponins, and Digitalis Analogues
    • Deobald, A. M.; Camargo, L. R. S.; Alves, D.; Zukerman-Schpector, J.; Corrêa, A. G.; Paixa'o, M. W. Click Chemistry: An Efficient Synthesis of Heterocycles Substituted with Steroids, Saponins, and Digitalis Analogues Synthesis 2011, 2011, 4003-4010 10.1055/s-0031-1289606
    • (2011) Synthesis , vol.2011 , pp. 4003-4010
    • Deobald, A.M.1    Camargo, L.R.S.2    Alves, D.3    Zukerman-Schpector, J.4    Corrêa, A.G.5    Paixa'o, M.W.6
  • 205
    • 84904490673 scopus 로고    scopus 로고
    • Preparation of Selectively Protected Protoescigenin Derivatives for Synthesis of Escin Analogs and Neoglycoconjugates
    • Jatczak, K.; Gruza, M.; Filip, K.; Cmoch, P.; Grynkiewicz, G. Preparation of Selectively Protected Protoescigenin Derivatives for Synthesis of Escin Analogs and Neoglycoconjugates Cent. Eur. J. Chem. 2014, 12, 1222-1231 10.2478/s11532-014-0572-9
    • (2014) Cent. Eur. J. Chem. , vol.12 , pp. 1222-1231
    • Jatczak, K.1    Gruza, M.2    Filip, K.3    Cmoch, P.4    Grynkiewicz, G.5
  • 206
    • 3242785011 scopus 로고    scopus 로고
    • Isoprenoids: Remarkable Diversity of Form and Function
    • Holstein, S. A.; Hohl, R. J. Isoprenoids: Remarkable Diversity of Form and Function Lipids 2004, 39, 293-309 10.1007/s11745-004-1233-3
    • (2004) Lipids , vol.39 , pp. 293-309
    • Holstein, S.A.1    Hohl, R.J.2
  • 207
    • 25844446180 scopus 로고    scopus 로고
    • The Allylic Azide Rearrangement: Achieving Selectivity
    • Feldman, A. K.; Colasson, B.; Sharpless, K. B.; Fokin, V. V. The Allylic Azide Rearrangement: Achieving Selectivity J. Am. Chem. Soc. 2005, 127, 13444-13445 10.1021/ja050622q
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 13444-13445
    • Feldman, A.K.1    Colasson, B.2    Sharpless, K.B.3    Fokin, V.V.4
  • 208
    • 60249090089 scopus 로고    scopus 로고
    • Synthesis of a Polyprenyl-type Library Containing 1,4-Disubstituted-1,2,3-triazoles with Anti-biofilm Activities Against Pseudoalteromonas sp
    • Praud-Tabaries, A.; Dombrowsky, L.; Bottzek, O.; Briand, J.-F.; Blache, Y. Synthesis of a Polyprenyl-type Library Containing 1,4-Disubstituted-1,2,3-triazoles with Anti-biofilm Activities Against Pseudoalteromonas sp Tetrahedron Lett. 2009, 50, 1645-1648 10.1016/j.tetlet.2009.01.125
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1645-1648
    • Praud-Tabaries, A.1    Dombrowsky, L.2    Bottzek, O.3    Briand, J.-F.4    Blache, Y.5
  • 209
    • 79951722365 scopus 로고    scopus 로고
    • Targeting Bacterial Biofilms: Design of a Terpenoid-like Library as Non-toxic Anti-biofilm Compounds
    • Sall, C.; Dombrowsky, L.; Bottzeck, O.; Praud-Tabariès, A.; Blache, Y. Targeting Bacterial Biofilms: Design of a Terpenoid-like Library as Non-toxic Anti-biofilm Compounds Bioorg. Med. Chem. Lett. 2011, 21, 1493-1497 10.1016/j.bmcl.2010.12.134
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 1493-1497
    • Sall, C.1    Dombrowsky, L.2    Bottzeck, O.3    Praud-Tabariès, A.4    Blache, Y.5
  • 210
    • 84921325836 scopus 로고    scopus 로고
    • Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
    • Palsuledesai, C. C.; Distefano, M. D. Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications ACS Chem. Biol. 2015, 10, 51-62 10.1021/cb500791f
    • (2015) ACS Chem. Biol. , vol.10 , pp. 51-62
    • Palsuledesai, C.C.1    Distefano, M.D.2
  • 212
    • 84899456383 scopus 로고    scopus 로고
    • Geranyl and Neryl Triazole Bisphosphonates as Inhibitors of Geranylgeranyl Diphosphate Synthase
    • Zhou, X.; Ferree, S. D.; Wills, V. S.; Born, E. J.; Tong, H.; Wiemer, D. F.; Holstein, S. A. Geranyl and Neryl Triazole Bisphosphonates as Inhibitors of Geranylgeranyl Diphosphate Synthase Bioorg. Med. Chem. 2014, 22, 2791-2798 10.1016/j.bmc.2014.03.014
    • (2014) Bioorg. Med. Chem. , vol.22 , pp. 2791-2798
    • Zhou, X.1    Ferree, S.D.2    Wills, V.S.3    Born, E.J.4    Tong, H.5    Wiemer, D.F.6    Holstein, S.A.7
  • 213
    • 84866644783 scopus 로고    scopus 로고
    • Synthesis of Farnesol Analogues Containing Triazoles in Place of Isoprenes through "Click Chemistry"
    • Subramanian, T.; Parkin, S.; Spielmann, H. P. Synthesis of Farnesol Analogues Containing Triazoles in Place of Isoprenes through "Click Chemistry" Synlett 2012, 23, 2539-2543 10.1055/s-0031-1290461
    • (2012) Synlett , vol.23 , pp. 2539-2543
    • Subramanian, T.1    Parkin, S.2    Spielmann, H.P.3
  • 214
    • 84855907701 scopus 로고    scopus 로고
    • S-Farnesyl-Thiopropionic Acid Triazoles as Potent Inhibitors of Isoprenylcysteine Carboxyl Methyltransferase
    • Bergman, J. A.; Hahne, K.; Song, J.; Hrycyna, C. A.; Gibbs, R. A. S-Farnesyl-Thiopropionic Acid Triazoles as Potent Inhibitors of Isoprenylcysteine Carboxyl Methyltransferase ACS Med. Chem. Lett. 2012, 3, 15-19 10.1021/ml200106d
    • (2012) ACS Med. Chem. Lett. , vol.3 , pp. 15-19
    • Bergman, J.A.1    Hahne, K.2    Song, J.3    Hrycyna, C.A.4    Gibbs, R.A.5
  • 215
    • 77953893928 scopus 로고    scopus 로고
    • Copper-free Click Chemistry Bioorthogonal Reagents for Tagging Azides
    • Baskin, J. M.; Bertozzi, C. R. Copper-free Click Chemistry Bioorthogonal Reagents for Tagging Azides Aldrichimica Acta 2010, 43, 15-23
    • (2010) Aldrichimica Acta , vol.43 , pp. 15-23
    • Baskin, J.M.1    Bertozzi, C.R.2
  • 217
    • 33846333918 scopus 로고    scopus 로고
    • Selective Labeling of Proteins by Using Protein Farnesyltransferase
    • Duckworth, B. P.; Zhang, Z.; Hosokawa, A.; Distefano, M. D. Selective Labeling of Proteins by Using Protein Farnesyltransferase ChemBioChem 2007, 8, 98-105 10.1002/cbic.200600340
    • (2007) ChemBioChem , vol.8 , pp. 98-105
    • Duckworth, B.P.1    Zhang, Z.2    Hosokawa, A.3    Distefano, M.D.4
  • 218
    • 34250015570 scopus 로고    scopus 로고
    • Evaluation of an Alkyne-containing Analogue of Farnesyl Diphosphate as a Dual Substrate for Protein-prenyltransferases
    • Hosokawa, A.; Wollack, J. W.; Zhang, Z.; Chen, L.; Barany, G.; Distefano, M. D. Evaluation of an Alkyne-containing Analogue of Farnesyl Diphosphate as a Dual Substrate for Protein-prenyltransferases Int. J. Pept. Res. Ther. 2007, 13, 345-354 10.1007/s10989-007-9090-3
    • (2007) Int. J. Pept. Res. Ther. , vol.13 , pp. 345-354
    • Hosokawa, A.1    Wollack, J.W.2    Zhang, Z.3    Chen, L.4    Barany, G.5    Distefano, M.D.6
  • 220
    • 84879730573 scopus 로고    scopus 로고
    • Prenylome Profiling Reveals S-farnesylation is Crucial for Membrane Targeting and Antiviral Activity of ZAP Long-isoform
    • Charron, G.; Li, M. M. H.; MacDonald, M. R.; Hang, H. C. Prenylome Profiling Reveals S-farnesylation is Crucial for Membrane Targeting and Antiviral Activity of ZAP Long-isoform Proc. Natl. Acad. Sci. U. S. A. 2013, 110, 11085-11090 10.1073/pnas.1302564110
    • (2013) Proc. Natl. Acad. Sci. U. S. A. , vol.110 , pp. 11085-11090
    • Charron, G.1    Li, M.M.H.2    MacDonald, M.R.3    Hang, H.C.4
  • 221
    • 80051786364 scopus 로고    scopus 로고
    • Evaluation of a Cell Penetrating Prenylated Peptide Lacking an Intrinsic Fluorophore via in situ Click Reaction
    • Ochocki, J. D.; Mullen, D. G.; Wattenberg, E. V.; Distefano, M. D. Evaluation of a Cell Penetrating Prenylated Peptide Lacking an Intrinsic Fluorophore via in situ Click Reaction Bioorg. Med. Chem. Lett. 2011, 21, 4998-5001 10.1016/j.bmcl.2011.04.138
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 4998-5001
    • Ochocki, J.D.1    Mullen, D.G.2    Wattenberg, E.V.3    Distefano, M.D.4
  • 222
    • 67651120082 scopus 로고    scopus 로고
    • Synthesis and Application of Photoaffinity Probe Containing an Intact Isoprenoid Chain
    • Li, L.; Tang, W.; Zhao, Z. K. Synthesis and Application of Photoaffinity Probe Containing an Intact Isoprenoid Chain Bioorg. Med. Chem. Lett. 2009, 19, 4824-4826 10.1016/j.bmcl.2009.06.037
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 4824-4826
    • Li, L.1    Tang, W.2    Zhao, Z.K.3
  • 224
    • 84896861606 scopus 로고    scopus 로고
    • 1,2,3-Triazole-Containing Derivatives of Rupestonic Acid: Click-chemical Synthesis and Antiviral Activities Against Influenza Viruses
    • He, Y.-W.; Dong, C.-Z.; Zhao, J.-Y.; ma, L.-L.; Li, Y.-H.; Aisa, H. A. 1,2,3-Triazole-Containing Derivatives of Rupestonic Acid: Click-chemical Synthesis and Antiviral Activities Against Influenza Viruses Eur. J. Med. Chem. 2014, 76, 245-255 10.1016/j.ejmech.2014.02.029
    • (2014) Eur. J. Med. Chem. , vol.76 , pp. 245-255
    • He, Y.-W.1    Dong, C.-Z.2    Zhao, J.-Y.3    Ma, L.-L.4    Li, Y.-H.5    Aisa, H.A.6
  • 225
    • 84901924951 scopus 로고    scopus 로고
    • Natural Sesquiterpene Lactones as Renewable Chemical Materials for New Medicinal Products
    • Adekenov, S. M. Natural Sesquiterpene Lactones as Renewable Chemical Materials for New Medicinal Products Eurasian Chem.-Technol. J. 2015, 15, 163-174 10.18321/ectj220
    • (2015) Eurasian Chem.-Technol. J. , vol.15 , pp. 163-174
    • Adekenov, S.M.1
  • 226
    • 80054071903 scopus 로고    scopus 로고
    • Perspectives on Sesquiterpene Lactones in Inflammation and Cancer
    • Merfort, I. Perspectives on Sesquiterpene Lactones in Inflammation and Cancer Curr. Drug Targets 2011, 12, 1560-1573 10.2174/138945011798109437
    • (2011) Curr. Drug Targets , vol.12 , pp. 1560-1573
    • Merfort, I.1
  • 227
    • 84893723977 scopus 로고    scopus 로고
    • Click Chemistry Inspired Facile Synthesis and Bioevaluation of Novel Triazolyl Analogs of Ludartin
    • Lone, S. H.; Bhat, K. A.; Majeed, R.; Hamid, A.; Khuroo, M. A. Click Chemistry Inspired Facile Synthesis and Bioevaluation of Novel Triazolyl Analogs of Ludartin Bioorg. Med. Chem. Lett. 2014, 24, 1047-1051 10.1016/j.bmcl.2014.01.018
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 1047-1051
    • Lone, S.H.1    Bhat, K.A.2    Majeed, R.3    Hamid, A.4    Khuroo, M.A.5
  • 229
    • 84916942936 scopus 로고    scopus 로고
    • Diterpenoids of Terrestrial Origin
    • Hanson, J. R. Diterpenoids of Terrestrial Origin Nat. Prod. Rep. 2015, 32, 76 10.1039/C4NP00108G
    • (2015) Nat. Prod. Rep. , vol.32 , pp. 76
    • Hanson, J.R.1
  • 230
    • 84863946239 scopus 로고    scopus 로고
    • Nat. Prod. Rep. 2012, 29, 890. 10.1039/c2np20051a
    • (2012) Nat. Prod. Rep. , vol.29 , pp. 890
  • 231
    • 84055186954 scopus 로고    scopus 로고
    • Nat. Prod. Rep. 2011, 28, 1755. 10.1039/c1np90021h
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 1755
  • 232
    • 70349504182 scopus 로고    scopus 로고
    • Nat. Prod. Rep. 2009, 26, 1156. 10.1039/b807311m
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 1156
  • 233
    • 84871880840 scopus 로고    scopus 로고
    • Progress in Renewable Polymers from Natural Terpenes, Terpenoids, and Rosin
    • Wilbon, P. A.; Chu, F.; Tang, C. Progress in Renewable Polymers from Natural Terpenes, Terpenoids, and Rosin Macromol. Rapid Commun. 2013, 34, 8-37 10.1002/marc.201200513
    • (2013) Macromol. Rapid Commun. , vol.34 , pp. 8-37
    • Wilbon, P.A.1    Chu, F.2    Tang, C.3
  • 234
    • 84874905056 scopus 로고    scopus 로고
    • Controlled Polymerization of Next-Generation Renewable Monomers and beyond
    • Yao, K.; Tang, C. Controlled Polymerization of Next-Generation Renewable Monomers and Beyond Macromolecules 2013, 46, 1689-1712 10.1021/ma3019574
    • (2013) Macromolecules , vol.46 , pp. 1689-1712
    • Yao, K.1    Tang, C.2
  • 236
    • 84894620086 scopus 로고    scopus 로고
    • Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid
    • Pertino, M. W.; Verdugo, V.; Theoduloz, C.; Schmeda-Hirschmann, G. Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid Molecules 2014, 19, 2523-2535 10.3390/molecules19022523
    • (2014) Molecules , vol.19 , pp. 2523-2535
    • Pertino, M.W.1    Verdugo, V.2    Theoduloz, C.3    Schmeda-Hirschmann, G.4
  • 237
    • 50249167106 scopus 로고    scopus 로고
    • A Click Chemistry Approach to Pleuromutilin Conjugates with Nucleosides or Acyclic Nucleoside Derivatives and Their Binding to the Bacterial Ribosome
    • Lolk, L.; Pøhlsgaard, J.; Jepsen, A. S.; Hansen, L. H.; Nielsen, H.; Steffansen, S. I.; Sparving, L.; Nielsen, A. B.; Vester, B.; Nielsen, P. A Click Chemistry Approach to Pleuromutilin Conjugates with Nucleosides or Acyclic Nucleoside Derivatives and Their Binding to the Bacterial Ribosome J. Med. Chem. 2008, 51, 4957-4967 10.1021/jm800261u
    • (2008) J. Med. Chem. , vol.51 , pp. 4957-4967
    • Lolk, L.1    Pøhlsgaard, J.2    Jepsen, A.S.3    Hansen, L.H.4    Nielsen, H.5    Steffansen, S.I.6    Sparving, L.7    Nielsen, A.B.8    Vester, B.9    Nielsen, P.10
  • 238
    • 84863242788 scopus 로고    scopus 로고
    • A Click Chemistry Approach to Pleuromutilin Derivatives, Part 2: Conjugates with Acyclic Nucleosides and Their Ribosomal Binding and Antibacterial Activity
    • Dreier, I.; Kumar, S.; Søndergaard, H.; Rasmussen, M. L.; Hansen, L. H.; List, N. H.; Kongsted, J.; Vester, B.; Nielsen, P. A Click Chemistry Approach to Pleuromutilin Derivatives, Part 2: Conjugates with Acyclic Nucleosides and Their Ribosomal Binding and Antibacterial Activity J. Med. Chem. 2012, 55, 2067-2077 10.1021/jm201266b
    • (2012) J. Med. Chem. , vol.55 , pp. 2067-2077
    • Dreier, I.1    Kumar, S.2    Søndergaard, H.3    Rasmussen, M.L.4    Hansen, L.H.5    List, N.H.6    Kongsted, J.7    Vester, B.8    Nielsen, P.9
  • 239
    • 84893724606 scopus 로고    scopus 로고
    • A Click Chemistry Approach to Pleuromutilin Derivatives. Part 3: Extended Footprinting Analysis and Excellent MRSA Inhibition for a Derivative with an Adenine Phenyl Side Chain
    • Dreier, I.; Hansen, L. H.; Nielsen, P.; Vester, B. A Click Chemistry Approach to Pleuromutilin Derivatives. Part 3: Extended Footprinting Analysis and Excellent MRSA Inhibition for a Derivative with an Adenine Phenyl Side Chain Bioorg. Med. Chem. Lett. 2014, 24, 1043-1046 10.1016/j.bmcl.2014.01.019
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 1043-1046
    • Dreier, I.1    Hansen, L.H.2    Nielsen, P.3    Vester, B.4
  • 240
    • 84878343968 scopus 로고    scopus 로고
    • Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
    • Pertino, M. W.; Theoduloz, C.; Bastías, M.; Schmeda-Hirschmann, G. Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects Molecules 2013, 18, 5936-5953 10.3390/molecules18055936
    • (2013) Molecules , vol.18 , pp. 5936-5953
    • Pertino, M.W.1    Theoduloz, C.2    Bastías, M.3    Schmeda-Hirschmann, G.4
  • 242
    • 84880554110 scopus 로고    scopus 로고
    • Overcoming Synthetic Challenges of Oridonin A-Ring Structural Diversification: Regio- and Stereoselective Installation of Azides and 1,2,3-Triazoles at the C-1, C-2, or C-3 Position
    • Ding, C.; Zhang, Y.; Chen, H.; Wild, Ch.; Wang, T.; White, M. A.; Shen, Q.; Zhou, J. Overcoming Synthetic Challenges of Oridonin A-Ring Structural Diversification: Regio- and Stereoselective Installation of Azides and 1,2,3-Triazoles at the C-1, C-2, or C-3 Position Org. Lett. 2013, 15, 3718-3721 10.1021/ol4015865
    • (2013) Org. Lett. , vol.15 , pp. 3718-3721
    • Ding, C.1    Zhang, Y.2    Chen, H.3    Wild, Ch.4    Wang, T.5    White, M.A.6    Shen, Q.7    Zhou, J.8
  • 243
    • 60449110147 scopus 로고    scopus 로고
    • Synthesis and Biological Evaluation of C-12 Triazole and Oxadiazole Analogs of Salvinorin A
    • Yang, L.; Xu, W.; Chen, F.; Liu-Chen, L.-Y.; Ma, Z.; Lee, D. Y. W. Synthesis and Biological Evaluation of C-12 Triazole and Oxadiazole Analogs of Salvinorin A Bioorg. Med. Chem. Lett. 2009, 19, 1301-1304 10.1016/j.bmcl.2009.01.078
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 1301-1304
    • Yang, L.1    Xu, W.2    Chen, F.3    Liu-Chen, L.-Y.4    Ma, Z.5    Lee, D.Y.W.6
  • 244
    • 77956148100 scopus 로고    scopus 로고
    • A Solanesol-derived Scaffold for Multimerization of Bioactive Peptides
    • Alleti, R.; Rao, V.; Xu, L.; Gillies, R. J.; Mash, E. A. A Solanesol-derived Scaffold for Multimerization of Bioactive Peptides J. Org. Chem. 2010, 75, 5895-5903 10.1021/jo101043m
    • (2010) J. Org. Chem. , vol.75 , pp. 5895-5903
    • Alleti, R.1    Rao, V.2    Xu, L.3    Gillies, R.J.4    Mash, E.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.