-
1
-
-
0011984675
-
1,2,3-Triazole
-
Schumann E (ed), Thieme, Stuttgart
-
Dehne H (1994) 1,2,3-Triazole. In: Schumann E (ed) Methoden der organischen chemie (Houben-Weyl), Vol E8d. Thieme, Stuttgart, pp 305-405
-
(1994)
Methoden der Organischen Chemie (Houben-Weyl)
, vol.E8D
, pp. 305-405
-
-
Dehne, H.1
-
2
-
-
84944077249
-
1,2,3-Triazoles
-
Katritzky AR, Rees CW, Scriven EFV (eds) Elsevier Science, Oxford, doi:10.1016/B978-008096518-5.00079-4
-
Fan W-Q, Katritzky AR (1996) 1,2,3-Triazoles. In: Katritzky AR, Rees CW, Scriven EFV (eds) Comprehensive heterocyclic chemistry II, Vol. 4. Elsevier Science, Oxford, pp 1-126. doi:10.1016/B978-008096518-5.00079-4
-
(1996)
Comprehensive Heterocyclic Chemistry II
, vol.4
, pp. 1-126
-
-
Fan, W.-Q.1
Katritzky, A.R.2
-
3
-
-
0020677250
-
Studies on v-triazoles. 7. Antiallergic 9-oxo-1H,9H-benzopyrano[2,3-d]-v- triazoles
-
DOI 10.1021/jm00356a025
-
Buckle DR, Outred DJ, Rockell CJM, Smith H, Spicer BA (1983) Studies on v-triazoles 7. Antiallergic 9-oxo-1H,9Hbenzopyrano[ 2,3-d]-v-triazoles. JMed Chem 26:251-254. doi:10.1021/jm00356a025 (Pubitemid 13187355)
-
(1983)
Journal of Medicinal Chemistry
, vol.26
, Issue.2
, pp. 251-254
-
-
Buckle, D.R.1
Outred, D.J.2
Rockell, C.J.M.3
-
4
-
-
0023018014
-
1-antihistamine and mast cell stabilizing properties
-
DOI 10.1021/jm00161a022
-
Buckle DR, Rockell CJM, Smith H, Spicer BA (1986) Studies on 1,2,3-triazoles 13. (Piperazinylalkoxy)[1]benzopyrano[2,3-d]-1,2,3-triazol-9(1H) -ones with combined H1-antihistamine and mast cell stabilizing properties. J Med Chem 29: 2262-2267. doi:10.1021/jm00161a022 (Pubitemid 17182304)
-
(1986)
Journal of Medicinal Chemistry
, vol.29
, Issue.11
, pp. 2262-2267
-
-
Buckle, D.R.1
Rockell, C.J.M.2
Smith, H.3
Spicer, B.A.4
-
5
-
-
0034624685
-
Substituent effects on the antibacterial activity of nitrogen-carbon- linked (azolylphenyl)oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenzae and Moraxella catarrhalis
-
DOI 10.1021/jm990373e
-
Genin MJ, Allwine BA, Anderson DJ, Barbachyn MR, Emmert DE, Garmon SA, Graber DR, Grega KC, Hester JB, Hutchinson DK, Morris J, Reischer RJ, Ford CW, Zurenko GE, Hamel JC, Schaadt RD, Stapert D, Yagi BH (2000) Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl) oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenza and Moraxella catarralis. J Med Chem 43:953-970. doi:10.1021/jm990373e (Pubitemid 30152301)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.5
, pp. 953-970
-
-
Genin, M.J.1
Allwine, D.A.2
Anderson, D.J.3
Barbachyn, M.R.4
Emmert, D.E.5
Garmon, S.A.6
Graber, D.R.7
Grega, K.C.8
Hester, J.B.9
Hutchinson, D.K.10
Morris, J.11
Reischer, R.J.12
Ford, C.W.13
Zurenko, G.E.14
Hamel, J.C.15
Schaadt, R.D.16
Stapert, D.17
Yagi, B.H.18
-
6
-
-
0037294865
-
Synthesis and investigation of tuberculosis inhibition activities of some 1,2,3-triazole derivatives
-
DOI 10.1016/S0223-5234(02)01445-9
-
Dabak K, Sezer Ö, Akar A, Olcay A (2003) Synthesis and investigation of tuberculosis inhibition activities of some 1,2,3-triazoles. Eur J Med Chem 38:215-218. doi:10.1016/S0223-5234(02)01445-9 (Pubitemid 36288475)
-
(2003)
European Journal of Medicinal Chemistry
, vol.38
, Issue.2
, pp. 215-218
-
-
Dabak, K.1
Sezer, O.2
Akar, A.3
Anac, O.4
-
7
-
-
0028063421
-
1,2,3-Triazole-[ 2′,5′-bis-O-(tert-butyldimethylsilyl)- â-D-ribofuranosyl]- 3′-spiro-5″-(4″-amino-1″, 2″-oxathiole 2″,2″-dioxide) (TSAO) analogues: Synthesis and anti-HIV-1 activity
-
doi:10.1021/jm00050a015
-
Alvarez R, Velázquez S, San-Félix A, Aquaro S, De Clercq E, PernoC-F, Karlsson A, Balzarini J, Camarasa MJ (1994) 1,2,3-Triazole-[ 2′,5′-bis-O-(tert-butyldimethylsilyl)-â-D-ribofuranosyl]- 3′-spiro-5″-(4″-amino-1″,2″-oxathiole 2″,2″-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activity. J Med Chem 37:4185-4194. doi:10.1021/jm00050a015
-
(1994)
J Med Chem
, vol.37
, pp. 4185-4194
-
-
Alvarez, R.1
Velázquez, S.2
San-Félix, A.3
Aquaro, S.4
De Clercq, E.5
Perno, C.-F.6
Karlsson, A.7
Balzarini, J.8
Camarasa, M.J.9
-
8
-
-
27644579969
-
Efficient Pd(0)-catalyzed synthesis of 1,2,3-triazolo-3′- deoxycarbanucleosides and their analogues
-
DOI 10.1016/j.tet.2005.09.034, PII S0040402005016054
-
Joubert N, Schinazi RF, Agrofoglio LA (2005) Efficient Pd(0)-catalyzed synthesis of 1,2,3-triazolo-3′-deoxycarbanucleosides and their analogues. Tetrahedron 61:11744-11750. doi:10.1016/j.tet.2005.09.034 (Pubitemid 41572618)
-
(2005)
Tetrahedron
, vol.61
, Issue.49
, pp. 11744-11750
-
-
Joubert, N.1
Schinazi, R.F.2
Agrofoglio, L.A.3
-
9
-
-
22844438442
-
Synthesis, characterization and biological activity of triorganotin 2-phenyl-1,2,3-triazole-4-carboxylates
-
DOI 10.1016/j.jinorgbio.2005.05.006, PII S0162013405001364
-
Tian L, Sun Y, Li H, Zheng X, Cheng Y, Liu X, Qian B (2005) Synthesis, characterization and biological activity of triorganotin 2-phenyl-1,2,3- triazole-4-carboxylates. J Inorg Biochem 99: 1646-1652. doi:10.1016/j.inorgbio. 2005.05.506 (Pubitemid 41039923)
-
(2005)
Journal of Inorganic Biochemistry
, vol.99
, Issue.8
, pp. 1646-1652
-
-
Tian, L.1
Sun, Y.2
Li, H.3
Zheng, X.4
Cheng, Y.5
Liu, X.6
Qian, B.7
-
10
-
-
1942534588
-
Synthesis and biological evaluation of novel 2-pyridinyl-[1,2,3]triazoles as inhibitors of transforming growth factor β1 type 1 receptor
-
DOI 10.1016/j.bmcl.2004.03.024, PII S0960894X04003579
-
Kim D-D, Kim J, Park H-J (2004) Synthesis and biological evaluation of novel 2-pyridinyl-[1,2,3]triazoles as inhibitors of transforming growth factor β1 type 1 receptor. Bioorg Med Chem Lett 14:2401-2405. doi:10.1016/j.bmcl. 2004.03.024 (Pubitemid 38515674)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.10
, pp. 2401-2405
-
-
Kim, D.-K.1
Kim, J.2
Park, H.-J.3
-
11
-
-
20644448817
-
3-(1,2,3-Triazol-1-yl)-1-thio-galactosides as small, efficient, and hydrolytically stable inhibitors of galectin-3
-
DOI 10.1016/j.bmcl.2005.05.084, PII S0960894X05006402
-
Salameh BA, Leffler H, Nilsson UJ (2005) 3-(1,2,3-Triazol-1-yl)-1- thiogalactosides as small, efficient hydrolytically stable inhibitors of galectin-3. Bioorg Med Chem Lett 15:3344-3346. doi:10.1016/j.bmcl.2005.05.084 (Pubitemid 40835732)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.14
, pp. 3344-3346
-
-
Salameh, B.A.1
Leffler, H.2
Nilsson, U.J.3
-
12
-
-
0036020059
-
1A receptor ligands
-
DOI 10.1016/S0928-0987(02)00045-3, PII S0928098702000453
-
Caliendo G, Fiorino F, Perissutti E, Severino B, Scolaro D, Gessi S, Cattabriga E, Borea PA, Santagada V (2002) A convenient synthesis by microwave heating and pharmacological evaluation of novel benzoyltriazole and saccharine derivatives as 5-HT1A receptor ligands. Eur J Pharm Sci 16:15-28. doi:10.1016/S0928-0987(02)00045-3 (Pubitemid 34756778)
-
(2002)
European Journal of Pharmaceutical Sciences
, vol.16
, Issue.1-2
, pp. 15-28
-
-
Caliendo, G.1
Fiorino, F.2
Perissutti, E.3
Severino, B.4
Scolaro, D.5
Gessi, S.6
Cattabriga, E.7
Borea, P.A.8
Santagada, V.9
-
13
-
-
19544383231
-
Benzoyl and/or benzyl substituted 1,2,3-triazoles as potassium channel activators. VIII
-
DOI 10.1016/j.ejmech.2005.01.010, PII S0223523405000292
-
Calderone V, Giorgi I, Livi O, Martinotti E, Mantuano E, Martelli A, Nardi A (2005) Benzoyl and/or benzyl substituted 1,2,3-triazoles as potassium channel activators. VIII. Eur J Med Chem 40:521-528. doi:10.1016/j.ejmech.2005. 01.010 (Pubitemid 40732521)
-
(2005)
European Journal of Medicinal Chemistry
, vol.40
, Issue.6
, pp. 521-528
-
-
Calderone, V.1
Giorgi, I.2
Livi, O.3
Martinotti, E.4
Mantuano, E.5
Martelli, A.6
Nardi, A.7
-
14
-
-
0001427691
-
1,3-Dipolare cycloadditionen: Ruckschau und ausblick
-
Huisgen R (1963) 1,3-Dipolare cycloadditionen: ruckschau und ausblick. Angew Chem 75:604-637
-
(1963)
Angew Chem
, vol.75
, pp. 604-637
-
-
Huisgen, R.1
-
15
-
-
84981452695
-
1,3-Dipolare Cycloadditionen, XXXII
-
Huisgen R, Szeimes G, Moebius L (1967) 1,3-Dipolare Cycloadditionen, XXXII. Chem Ber 100:2494-2507
-
(1967)
Chem Ber
, vol.100
, pp. 2494-2507
-
-
Huisgen, R.1
Szeimes, G.2
Moebius, L.3
-
16
-
-
84986442078
-
Synthese von pyrazol- und triazoldialdehyden
-
Henkel K, Weygand F (1943) Synthese von pyrazol- und triazoldialdehyden. Chem Ber 76:812-818
-
(1943)
Chem Ber
, vol.76
, pp. 812-818
-
-
Henkel, K.1
Weygand, F.2
-
17
-
-
0037012920
-
Peptidotriazoles on solid phase: [1,2,3]-Triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
-
DOI 10.1021/jo011148j
-
Tornøe CW, Christensen C, Meldal M (2002) 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 67:3057-3064. doi:10.1021/jo011148j (Pubitemid 34457265)
-
(2002)
Journal of Organic Chemistry
, vol.67
, Issue.9
, pp. 3057-3064
-
-
Tornoe, C.W.1
Christensen, C.2
Meldal, M.3
-
18
-
-
0037099395
-
A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
doi:10.1002/1521-3773(20020715)41: 14〈2596::AID-ANIE2596〉3.0. CO;2-4
-
Rostovtsev VV, Green LG, Fokin VV, Sharpless KB (2002) A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew Chem Int Ed 41:2596-2599. doi:10.1002/1521-3773(20020715)41: 14〈2596::AID-ANIE2596〉3.0.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
-
19
-
-
28044465418
-
Ruthenium-catalyzed cycloaddition of alkynes and organic azides
-
DOI 10.1021/ja054114s
-
Zhang L, Chen X, Xue P, Sun HHY, Williams ID, Sharpless KB, Fokin V, Jia G (2005) Ruthenium-catalyzed cycloaddition of alkynes and organic azides. J Am Chem Soc 127:15998-15999. doi:10.1021/ja054114s (Pubitemid 41689208)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.46
, pp. 15998-15999
-
-
Zhang, L.1
Chen, X.2
Xue, P.3
Sun, H.H.Y.4
Williams, I.D.5
Sharpless, K.B.6
Fokin, V.V.7
Jia, G.8
-
20
-
-
84867726453
-
CuI-catalyzed alkyne-azide "click" cycloadditions from a mechanistic and synthetic perspective
-
doi:10.1002/ejoc.200500483
-
Bock VD, Hiemstra H, van Maarseveen JH (2006) CuI-catalyzed alkyne-azide "click" cycloadditions from a mechanistic and synthetic perspective. Eur J Org Chem 51-68. doi:10.1002/ejoc.200500483
-
(2006)
Eur J Org Chem
, pp. 51-68
-
-
Bock, V.D.1
Hiemstra, H.2
Van Maarseveen, J.H.3
-
21
-
-
34250811485
-
The rise of azide-alkyne 1,3-dipolar 'click' cycloaddition and its application to polymer science and surface modification
-
doi:10.1071/CH06457
-
Evans RA (2007) The rise of azide-alkyne 1,3-dipolar 'click' cycloaddition and its application to polymer science and surface modification. Aust J Chem 60:384-395. doi:10.1071/CH06457
-
(2007)
Aust J Chem
, vol.60
, pp. 384-395
-
-
Evans, R.A.1
-
22
-
-
34547272503
-
The growing applications of click chemistry
-
doi:10.1039/B613014N
-
Moses JE, Moorhouse AD (2007) The growing applications of click chemistry. Chem Soc Rev 36:1249-1262. doi:10.1039/B613014N
-
(2007)
Chem Soc Rev
, vol.36
, pp. 1249-1262
-
-
Moses, J.E.1
Moorhouse, A.D.2
-
23
-
-
39549111477
-
Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes
-
DOI 10.1002/med.20107
-
Tron GC, Pirali T, Billington RA, Canonico PL, Sorba G, Genazzani AA (2008) Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloadditions between azides and alkynes. Med Res Rev 28:278-308. doi:10.1002/med.20107 (Pubitemid 351281190)
-
(2008)
Medicinal Research Reviews
, vol.28
, Issue.2
, 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
-
24
-
-
77949799806
-
Click chemistry under non-classical reaction conditions
-
doi:10.1039/B901973C
-
Kappe CO, van der Eycken E (2010) Click chemistry under non-classical reaction conditions. Chem Soc Rev 39:1280-1290. doi:10.1039/B901973C
-
(2010)
Chem Soc Rev
, vol.39
, pp. 1280-1290
-
-
Kappe, C.O.1
Van Der Eycken, E.2
-
25
-
-
11844255741
-
Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates
-
doi:10.1021.ja0471525
-
Himo F, Lovell T, Hilgraf R, Rostovcev VV, Noodleman L, Sharpless KB, Fokin VV (2005) Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates. J Am Chem Soc 127:210-216. doi:10.1021.ja0471525
-
(2005)
J Am Chem Soc
, vol.127
, pp. 210-216
-
-
Himo, F.1
Lovell, T.2
Hilgraf, R.3
Rostovcev, V.V.4
Noodleman, L.5
Sharpless, K.B.6
Fokin, V.V.7
-
26
-
-
4444324951
-
Polytriazoles as copper(I)-stabilizing ligands in catalysis
-
DOI 10.1021/ol0493094
-
Chan TR, Hilgraf R, Sharpless KB, Fokin VV (2004) Polytriazoles as copper(I)-stabilizing ligands in catalysis.Org Lett 6:2853-2855. doi:10.1021/ol0493094 (Pubitemid 39178025)
-
(2004)
Organic Letters
, vol.6
, Issue.17
, pp. 2853-2855
-
-
Chan, T.R.1
Hilgraf, R.2
Sharpless, K.B.3
Fokin, V.V.4
-
27
-
-
9444260351
-
A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction
-
Appukkuttan P, Dehaen W, Fokin VV, van der Eycken E (2004) A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via copper(I)-catalyzed three-component reaction. Org Lett 6:4223-4225. doi:10.1021/ol048341v (Pubitemid 39563449)
-
(2004)
Organic Letters
, vol.6
, Issue.23
, pp. 4223-4225
-
-
Appukkuttan, P.1
Dehaen, W.2
Fokin, V.V.3
Van Der, E.E.4
-
28
-
-
79960246251
-
Conventional and microwave assisted synthesis of 1,4-disubstituted 1,2,3-triazoles from Huisgen cycloaddition
-
Sarmiento-Sánchez JI, Ochoa-Terán A, Rivero IA (2011) Conventional and microwave assisted synthesis of 1,4-disubstituted 1,2,3-triazoles from Huisgen cycloaddition. ARKIVOC ix:177-188
-
(2011)
ARKIVOC
, vol.9
, pp. 177-188
-
-
Sarmiento-Sánchez, J.I.1
Ochoa-Terán, A.2
Rivero, I.A.3
-
29
-
-
0141629513
-
Multivalent neoglycoconjugates by regioselective cycloaddition of alkynes and azides using organicsoluble copper catalysts
-
doi:10.1021/ol034534r
-
Pérez-Balderas F, Ortega-Muñoz M, Morales-Sanfrutos J, Hernández-Mateo F, Calvo-Flores FG, Calvo-Asín JA, Isac-García J, Santoyo-González F (2003) Multivalent neoglycoconjugates by regioselective cycloaddition of alkynes and azides using organicsoluble copper catalysts. Org Lett 5:1951-1954. doi:10.1021/ol034534r
-
(2003)
Org Lett
, vol.5
, pp. 1951-1954
-
-
Pérez-Balderas, F.1
Ortega-Muñoz, M.2
Morales-Sanfrutos, J.3
Hernández-Mateo, F.4
Calvo-Flores, F.G.5
Calvo-Asín, J.A.6
Isac-García, J.7
Santoyo-González, F.8
-
30
-
-
4644340517
-
Copper-catalyzed synthesis of N-unsubstituted 1,2,3-triazoles from nonactivated terminal alkynes
-
doi:10.1002/ejoc.200400442
-
Jin T, Kamijo S, Yamamoto Y (2004) Copper-catalyzed synthesis of N-unsubstituted 1,2,3-triazoles from nonactivated terminal alkynes. Eur J Org Chem 18:3789-3791 doi:10.1002/ejoc.200400442
-
(2004)
Eur J Org Chem
, vol.18
, pp. 3789-3791
-
-
Jin, T.1
Kamijo, S.2
Yamamoto, Y.3
-
32
-
-
4444233074
-
Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(I)-catalyzed ligation of azides and alkynes
-
DOI 10.1002/anie.200454078
-
Wu P, Feldman AK, Nugent AK, Hawker CJ, Scheel A, Voit B, Pyun J, Fréchet JMJ, Sharpless KB, Fokin VV (2004) Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(I)-catalyzed ligation of azides and alkynes. Angew Chem Int Ed 43:3928-3932. doi:10.1002/anie. 200454078 (Pubitemid 39257472)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.30
, pp. 3928-3932
-
-
Wu, P.1
Feldman, A.K.2
Nugent, A.K.3
Hawker, C.J.4
Scheel, A.5
Voit, B.6
Pyun, J.7
Frechet, J.M.J.8
Sharpless, K.B.9
Fokin, V.V.10
-
33
-
-
18244371903
-
Efficient synthesis of water-soluble calixarenes using click chemistry
-
DOI 10.1021/ol047468h
-
Ryu E-H, Zhao Y (2005) Efficient synthesis ofwater-soluble calixarenes using click chemistry. Org Lett 7:1035-1037. doi:10.1021/ol047468h (Pubitemid 40626894)
-
(2005)
Organic Letters
, vol.7
, Issue.6
, pp. 1035-1037
-
-
Ryu, E.-H.1
Zhao, Y.2
-
34
-
-
10044258626
-
A fluorogenic 1,3-dipolar cycloaddition reaction of 3-azidocoumarins and acetylenes
-
DOI 10.1021/ol047955x
-
Sivakumar K, Xie F, Cash BM, Long S, Barnhill HN, Wang Q (2004) A fluorogenic 1,3-dipolar cycloaddition reaction of 3-azidocoumarins and acetylenes. Org Lett 6:4603-4606. doi:10.1021/ol047955x (Pubitemid 39611821)
-
(2004)
Organic Letters
, vol.6
, Issue.24
, pp. 4603-4606
-
-
Sivakumar, K.1
Xie, F.2
Cash, B.M.3
Long, S.4
Barnhill, H.N.5
Wang, Q.6
-
35
-
-
0037021535
-
Synthesis of sugar arrays in microtiter plate
-
DOI 10.1021/ja020887u
-
Fazio F, Bryan MC, Blixt O, Paulson JC, Wong C-H (2002) Synthesis of sugar arrays in microtiter plate. J Am Chem Soc 124:14397-14402. doi:10.1021/ja020887u (Pubitemid 35403761)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.48
, pp. 14397-14402
-
-
Fazio, F.1
Bryan, M.C.2
Blixt, O.3
Paulson, J.C.4
Wong, C.-H.5
-
36
-
-
9344238756
-
Combining biginelli multicomponent and click chemistry: Generation of 6-(1,2,3-triazol-1-yl)-dihydropyrimidone libraries
-
DOI 10.1021/cc0498938
-
Khanetskyy B, Dallinger D, Kappe CO (2004) CombiningBiginelli multicomponent and click chemistry: generation of 6-(1,2,3-triazol-1-yl)- dihydropyrimidone libraries. J Comb Chem 6:884-892. doi:10.1021/cc0498938 (Pubitemid 39556558)
-
(2004)
Journal of Combinatorial Chemistry
, vol.6
, Issue.6
, pp. 884-892
-
-
Khanetskyy, B.1
Dallinger, D.2
Kappe, C.O.3
-
37
-
-
0141518157
-
Click linker: Efficient and high-yielding synthesis of a new family of SPOS resins by 1,3-dipolar cycloaddition
-
DOI 10.1021/ol034520l
-
Löber S, Rodriguez-Loaiza P, Gmeiner P (2003) Click linker: efficient and high yielding synthesis of a new family of SPOS resins by 1,3-dipolar cycloaddition. Org Lett 5:1753-1755. doi:10.1021/ol034520l (Pubitemid 37162021)
-
(2003)
Organic Letters
, vol.5
, Issue.10
, pp. 1753-1755
-
-
Lober, S.1
Rodriguez-Loaiza, P.2
Gmeiner, P.3
-
38
-
-
1842714290
-
Click chemistry on surfaces: 1,3-dipolar cycloaddition reactions of azide-terminated monolayers on silica
-
doi:10.1021/jp049601t
-
Lummerstorfer T, Hoffmann H (2004) Click chemistry on surfaces: 1,3-dipolar cycloaddition reactions of azide-terminated monolayers on silica. J Phys Chem B 108:3963-3966. doi:10.1021/jp049601t
-
(2004)
J Phys Chem B
, vol.108
, pp. 3963-3966
-
-
Lummerstorfer, T.1
Hoffmann, H.2
-
39
-
-
0037454346
-
Bioconjugation by copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition
-
DOI 10.1021/ja021381e
-
Wang Q, Chan TR, Hilgraf R, Fokin VV, Sharpless KB, Finn MG (2003) Bioconjugation by copper(I)-catalyzed azide-alkyne [3+2] cycloaddition. J Am Chem Soc 125:3192-3193. doi:10.1021/ja021381e (Pubitemid 36512443)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.11
, pp. 3192-3193
-
-
Wang, Q.1
Chan, T.R.2
Hilgraf, R.3
Fokin, V.V.4
Sharpless, K.B.5
Finn, M.G.6
-
40
-
-
0037462106
-
Activity-based protein profiling in vivo using a copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition
-
DOI 10.1021/ja034490h
-
Speers AE, Adam GC, Cravatt BF (2003) Activity-based protein profiling in vivo using a copper(I)-catalyzed azide-alkyne [3+2] cycloaddition. J Am Chem Soc 125:4686-4687. doi:10.1021/ja034490h (Pubitemid 36505343)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.16
, pp. 4686-4687
-
-
Speers, A.E.1
Adam, G.C.2
Cravatt, B.F.3
-
41
-
-
9344227358
-
A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems
-
DOI 10.1021/ja044996f
-
Agard NJ, Prescher JA, Bertozzi CR (2004) A strain-promoted [3+2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems. J Am Chem Soc 126:15046-15047. doi:10.1021/ja044996f (Pubitemid 39557262)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.46
, pp. 15046-15047
-
-
Agard, N.J.1
Prescher, J.A.2
Bertozzi, C.R.3
-
42
-
-
79954573197
-
Syntheses and transformations of á-azido ketones and related derivatives
-
doi:10.1039/c0cs00101e
-
Patonay T, Kónya K, Juhász-Tóth É (2011) Syntheses and transformations of á-azido ketones and related derivatives. Chem Soc Rev 40:2797-2847. doi:10.1039/c0cs00101e
-
(2011)
Chem Soc Rev
, vol.40
, pp. 2797-2847
-
-
Patonay, T.1
Kónya, K.2
Juhász-Tóth, É.3
-
43
-
-
79954593410
-
2-Azido-2-substituted indan-1,3-dione
-
Gudrinietce E, Bruvele N, Ievins A (1966) 2-Azido-2-substituted indan-1,3-dione. Dokl Akad Nauk SSSR 171:869-871,
-
(1966)
Dokl Akad Nauk SSSR
, vol.171
, pp. 869-871
-
-
Gudrinietce, E.1
Bruvele, N.2
Ievins, A.3
-
44
-
-
84858699877
-
-
Chem Abstr (1967) 67:53900h
-
(1967)
Chem Abstr
, vol.67
-
-
-
45
-
-
27144467716
-
1,3-Dipolar cycloaddition reactions in heterocyclic synthesis. Synthesis of 1-[4-(thiazolyl/imidazothiazolyl/triazolyl)phenyl]-1H-pyrazole-3,4- dicarboxylate esters from 3-(4-acetylphenyl)sydnone
-
Hunnur RK, Latthe PR, Badami BV (2005) 1,3-Dipolar cycloaddition reactions in heterocyclic synthesis. Synthesis of [1-[4-(thiazolyl/ imidazothiazolyl/triazolyl)phenyl]-1H-pyrazole-3,4-dicarboxylate esters from 3-(4-acetylphenyl)sydnone. J Chem Res 9:592-594. doi:10.3184/030823405774308907 (Pubitemid 41494380)
-
(2005)
Journal of Chemical Research
, Issue.9
, pp. 592-594
-
-
Hunnur, R.K.1
Latthe, P.R.2
Badami, B.V.3
-
46
-
-
19544378528
-
Click to fit: Versatile polyvalent display on a peptidomimetic scaffold
-
DOI 10.1021/ol050371q
-
Jang H, Fafarman A, Holub JM, Kirshenbaum K (2005) Click to fit: versatile polyvalent display on a peptidomimetic scaffold. Org Lett 7:1951-1954. doi:10.1021/ol050371q (Pubitemid 40732021)
-
(2005)
Organic Letters
, vol.7
, Issue.10
, pp. 1951-1954
-
-
Jang, H.1
Fafarman, A.2
Holub, J.M.3
Kirshenbaum, K.4
-
47
-
-
62249172981
-
Greener and expeditious synthesis of 1,4-disubstituted 1,2,3-triazoles from terminal acetylenes and in situ generated α-azido ketones
-
doi:10.1055/s-0028-1087556
-
Kumar D, Patel G, Reddy VB (2009) Greener and expeditious synthesis of 1,4-disubstituted 1,2,3-triazoles from terminal acetylenes and in situ generated α-azido ketones. Synlett 20:399-402. doi:10.1055/s-0028-1087556
-
(2009)
Synlett
, vol.20
, pp. 399-402
-
-
Kumar, D.1
Patel, G.2
Reddy, V.B.3
-
48
-
-
62449166392
-
A facile and regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles by click chemistry
-
doi:10.1016/j.tetlet.2009.02.107
-
Kumar D, Reddy VB, Varma RS (2009) A facile and regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles by click chemistry. Tetrahedron Lett 50:2065-2068. doi:10.1016/j.tetlet.2009.02.107
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 2065-2068
-
-
Kumar, D.1
Reddy, V.B.2
Varma, R.S.3
-
49
-
-
77957825923
-
Synthesis and cytotoxicity evaluation of novel 1,4-disubstituted 1,2,3-triazoles via CuI catalyzed 1,3-dipolar cycloaddition
-
doi:10.1016/ ejmech.2010.08.012
-
Vantikommu J, Palle S, Reddy PS, Ramanatham V, Khagga M, Pallapothula VR (2010) Synthesis and cytotoxicity evaluation of novel 1,4-disubstituted 1,2,3-triazoles via CuI catalyzed 1,3-dipolar cycloaddition. Eur J Med Chem 45:5044-5050. doi:10.1016/ ejmech.2010.08.012
-
(2010)
Eur J Med Chem
, vol.45
, pp. 5044-5050
-
-
Vantikommu, J.1
Palle, S.2
Reddy, P.S.3
Ramanatham, V.4
Khagga, M.5
Pallapothula, V.R.6
-
50
-
-
77953959578
-
Tandem oxidative α-tosyloxylation of alcohols/nucleophilic addition of azide/copper-catalyzed 1,3-dipolar cycloaddition
-
doi:10.1055/s0029-1217034
-
Reddy PS, Sreedhar B (2009) Tandem oxidative α-tosyloxylation of alcohols/nucleophilic addition of azide/copper-catalyzed 1,3-dipolar cycloaddition. Synthesis 4203-4207. doi:10.1055/s0029-1217034
-
(2009)
Synthesis
, pp. 4203-4207
-
-
Reddy, P.S.1
Sreedhar, B.2
-
51
-
-
77957896219
-
Carboxylic acid-promoted copper(I)-catalyzed azide-alkyne cycloaddition
-
doi:10.1021/jo101495k
-
Shao C, Wang X, Xu J, Zhao J, Zhang Q, Hu Y (2010) Carboxylic acid-promoted copper(I)-catalyzed azide-alkyne cycloaddition. J Org Chem 75:7002-7005. doi:10.1021/jo101495k
-
(2010)
J Org Chem
, vol.75
, pp. 7002-7005
-
-
Shao, C.1
Wang, X.2
Xu, J.3
Zhao, J.4
Zhang, Q.5
Hu, Y.6
-
52
-
-
77955926541
-
D-Ring substituted 1,2,3-triazolyl 20-keto pregnenanes as potential anticancer agents: Synthesis and biological evaluation
-
doi:10.1016/steroids.2010.02.015
-
Banday AH, Shameem AS, Gupta BD, Kumar HMS (2010) D-Ring substituted 1,2,3-triazolyl 20-keto pregnenanes as poten- tial anticancer agents: synthesis and biological evaluation. Steroids 75:801-804. doi:10.1016/steroids.2010.02.015
-
(2010)
Steroids
, vol.75
, pp. 801-804
-
-
Banday, A.H.1
Shameem, A.S.2
Gupta, B.D.3
Kumar, H.M.S.4
-
53
-
-
79960417422
-
Michael addition of α-azido ketones on iminocoumarin derivatives: And efficient access to new functionalized azido chromenes
-
doi:10.1016/j.tetlet.2011.05.101
-
Babu TH, Kamalraja J, Muralidharan D, Perumal PT (2011) Michael addition of α-azido ketones on iminocoumarin derivatives: and efficient access to new functionalized azido chromenes. Tetrahedron Lett 52:4093-4096. doi:10.1016/j.tetlet.2011.05.101
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 4093-4096
-
-
Babu, T.H.1
Kamalraja, J.2
Muralidharan, D.3
Perumal, P.T.4
-
54
-
-
33744966628
-
A new solvent system for efficient synthesis of 1,2,3-triazoles
-
DOI 10.1016/j.tetlet.2006.05.079, PII S0040403906010045
-
Lee B-Y, Park SR, Jeon HB, Kim KS (2006) A new solvent system for efficient synthesis of 1,2,3-triazoles. Tetrahedron Lett 47: 5105-5109. doi:10.1016/j.tetlet.2006.05.079 (Pubitemid 43867620)
-
(2006)
Tetrahedron Letters
, vol.47
, Issue.29
, pp. 5105-5109
-
-
Lee, B.-Y.1
Park, S.R.2
Jeon, H.B.3
Kim, K.S.4
-
55
-
-
0029994515
-
An efficient synthesis of the indole acetic acid metabolite of MK-0462
-
doi:10. 1080/00397919608003552
-
Chen C-Y, Lieberman DR, Street LJ, Guiblin AR, Larsen RD, Verhoeven TR (1996) An efficient synthesis of the indole acetic acid metabolite of MK-0462. Synth Comm 26:1977-1984. doi:10. 1080/00397919608003552
-
(1996)
Synth Comm
, vol.26
, pp. 1977-1984
-
-
Chen, C.-Y.1
Lieberman, D.R.2
Street, L.J.3
Guiblin, A.R.4
Larsen, R.D.5
Verhoeven, T.R.6
-
56
-
-
49049092768
-
A concise synthesis of (-) indolmycin and (-)-5-methoxyindolmycin
-
doi:10.1016/j.tetasy.2008.07.013
-
Sutou N, Kato K, Akita H (2008) A concise synthesis of (-) indolmycin and (-)-5-methoxyindolmycin. Tetrahedron Asymmetr 19:1833-1838. doi:10.1016/j.tetasy.2008.07.013
-
(2008)
Tetrahedron Asymmetr
, vol.19
, pp. 1833-1838
-
-
Sutou, N.1
Kato, K.2
Akita, H.3
-
57
-
-
33845277870
-
Cross-coupling of organosilanes with organic halides mediated by a palladium catalyst and tris(diethylamino)sulfonium difluorotrimethylsilicate
-
doi:10.1021/jo00239a056
-
Hatanaka Y, Hiyama T (1988) Cross-coupling of organosilanes with organic halides mediated by a palladium catalyst and tris(diethylamino)sulfonium difluorotrimethylsilicate. J Org Chem 53:918-920. doi:10.1021/jo00239a056
-
(1988)
J Org Chem
, vol.53
, pp. 918-920
-
-
Hatanaka, Y.1
Hiyama, T.2
-
58
-
-
14844349847
-
Hiyama cross-coupling of chloro-, fluoro-, and methoxypyridyltrimethylsilanes: Room-temperature novel access to functional bi(het)aryl
-
doi:10. 1021/ol047482u
-
Pierrat P, Gros P, Fort Y (2005) Hiyama cross-coupling of chloro-, fluoro-, and methoxypyridyltrimethylsilanes: room-temperature novel access to functional bi(het)aryl. Org Lett 7:697-700. doi:10. 1021/ol047482u
-
(2005)
Org Lett
, vol.7
, pp. 697-700
-
-
Pierrat, P.1
Gros, P.2
Fort, Y.3
-
59
-
-
0036154219
-
Base-induced coupling of α-azido ketones with aldehydes - An easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones, 2-acylaziridines, and 2-acylspiroaziridines
-
doi:10.1002/1099-0690(20021)2002:2<285::AID-EJOC285>3.0.CO;2-J
-
Patonay T, Juhász-Tóth É, Bényei A (2002) Base-induced coupling of α-azido ketones with aldehydes - an easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones, 2-acylaziridines, and 2-acylspiroaziridines. Eur J Org Chem 285-295. doi:10.1002/1099-0690(20021)2002:2<285::AID-EJOC285>3.0.CO;2-J
-
(2002)
Eur J Org Chem
, pp. 285-295
-
-
Patonay, T.1
Juhász-Tóth, É.2
Bényei, A.3
-
60
-
-
0036714739
-
Synthesis of tetrafunctionalized 2-azido-3-hydroxy-1,4-diones and their transformation into 5-substituted 3-acylisoxazoles
-
doi:10.1002/1099-0690(200209)2002:17〈3055::AID-EJOC3055〉3.0. CO;2-8
-
Juhász-TóthÉ, Patonay T (2002) Synthesis of tetrafunctionalized 2-azido-3-hydroxy-1,4-diones and their transformation into 5-substituted 3-acylisoxazoles. Eur J Org Chem 3055-3064. doi:10.1002/1099- 0690(200209)2002:17〈3055::AID-EJOC3055〉3.0.CO;2-8
-
(2002)
Eur J Org Chem
, pp. 3055-3064
-
-
Juhász-Tóth, É.1
Patonay, T.2
|