-
2
-
-
45349100212
-
From multicomponent-reactions (MCRs) towards multi-function-component- reactions (MFCRs)
-
Eckert, H. From multicomponent-reactions (MCRs) towards multi-function-component-reactions (MFCRs). Heterocycles 2007, 73, 149-158.
-
(2007)
Heterocycles
, vol.73
, pp. 149-158
-
-
Eckert, H.1
-
3
-
-
84984559459
-
-
Elsevier: New York, NY, USA
-
Katritzky, A.R., Ramsden, C.A., Scriven, E.F.V., Taylor, R.J.K., Eds. Comprehensive Heterocyclic Chemistry III; Elsevier: New York, NY, USA, 2008.
-
(2008)
Comprehensive Heterocyclic Chemistry III
-
-
Katritzky, A.R.1
Ramsden, C.A.2
Scriven, E.F.V.3
Taylor, R.J.K.4
-
4
-
-
0003851576
-
-
2nd ed.; Wiley & Sons: New York, NY, USA
-
Pozharskii, A.F.; Soldatenkov, A.T.; Katritzky, A.R. Heterocycles in Life and Society, 2nd ed.; Wiley & Sons: New York, NY, USA, 2011.
-
(2011)
Heterocycles in Life and Society
-
-
Pozharskii, A.F.1
Soldatenkov, A.T.2
Katritzky, A.R.3
-
5
-
-
80053341823
-
Heterocyclic chemistry
-
Hemming, K. Heterocyclic chemistry. Annu. Rep. Prog. Chem. B 2011, 107, 118-137.
-
(2011)
Annu. Rep. Prog. Chem. B
, vol.107
, pp. 118-137
-
-
Hemming, K.1
-
6
-
-
0004270887
-
-
Academic Press: New York, NY, USA
-
Ugi, I., Ed. Isonitrile Chemistry; Academic Press: New York, NY, USA, 1971.
-
(1971)
Isonitrile Chemistry
-
-
Ugi, I.1
-
7
-
-
79959799404
-
-
Topics in Heterocyclic Chemistry; Springer Verlag: New York, NY, USA
-
Orru, R.V.A., Ruijter, E., Eds. Synthesis of Heterocycles via Multicomponent Reactions I; Topics in Heterocyclic Chemistry; Springer Verlag: New York, NY, USA, 2010; Volume 23.
-
(2010)
Synthesis of Heterocycles via Multicomponent Reactions I
, vol.23
-
-
Orru, R.V.A.1
Ruijter, E.2
-
8
-
-
79959799404
-
-
Topics in Heterocyclic Chemistry; Springer Verlag: New York, NY, USA
-
Orru, R.V.A., Ruijter, E., Eds. Synthesis of Heterocycles via Multicomponent Reactions II; Topics in Heterocyclic Chemistry; Springer Verlag: New York, NY, USA, 2010; Volume 25.
-
(2010)
Synthesis of Heterocycles via Multicomponent Reactions II
, vol.25
-
-
Orru, R.V.A.1
Ruijter, E.2
-
9
-
-
84981761088
-
Über eine neue Darstellungsweise für substituierte Indole
-
Madelung, W. Über eine neue Darstellungsweise für substituierte Indole. Ber. Dtsch. Chem. Ges. 1912, 45, 1128.
-
(1912)
Ber. Dtsch. Chem. Ges.
, vol.45
, pp. 1128
-
-
Madelung, W.1
-
10
-
-
0019815529
-
Lithiation of N-(2-alkylphenyl)alkanamides and related compounds. A modified Madelung indole synthesis
-
Houlihan, W.J.; Parrino, V.A.; Uike, Y. Lithiation of N-(2-alkylphenyl)-alkanamides and related compounds. A modified Madelung indole synthesis. J. Org. Chem. 1981, 46, 4511-4515. (Pubitemid 12194519)
-
(1981)
Journal of Organic Chemistry
, vol.46
, Issue.22
, pp. 4511-4515
-
-
Houlihan, W.J.1
Parrino, V.A.2
Uike, Y.3
-
11
-
-
0000034629
-
An efficient synthesis of indole
-
Ito, Y.; Kobayashi, K.; Saegusa, T. An efficient synthesis of indole. J. Am. Chem. Soc. 1977, 99, 3532-3534.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 3532-3534
-
-
Ito, Y.1
Kobayashi, K.2
Saegusa, T.3
-
12
-
-
3042799070
-
A planning strategy for diversity-oriented synthesis
-
Burke, M.D.; Schreiber, S.L. A planning strategy for diversity-oriented synthesis. Angew. Chem. Int. Ed. Engl. 2004, 43, 47-58.
-
(2004)
Angew. Chem. Int. Ed. Engl.
, vol.43
, pp. 47-58
-
-
Burke, M.D.1
Schreiber, S.L.2
-
13
-
-
60749120878
-
Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds
-
Sunderhaus, J.D.; Martin, S.F. Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds. Chem. Eur. J. 2009, 15, 1300-1308.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 1300-1308
-
-
Sunderhaus, J.D.1
Martin, S.F.2
-
14
-
-
79959743947
-
Expeditious construction of spiro-pyrrolidines by an autocatalytic one-pot, five-component, 1,3-dipolar cycloaddition of in situ generated azo-methine ylides and olefinic dipolarophiles
-
Li, M.; Gong, F.-M.; Wen, L.-R.; Li, Z.-R. Expeditious construction of spiro-pyrrolidines by an autocatalytic one-pot, five-component, 1,3-dipolar cycloaddition of in situ generated azo-methine ylides and olefinic dipolarophiles. Eur. J. Org. Chem. 2011, 2011, 3482-3490.
-
(2011)
Eur. J. Org. Chem.
, vol.2011
, pp. 3482-3490
-
-
Li, M.1
Gong, F.-M.2
Wen, L.-R.3
Li, Z.-R.4
-
15
-
-
0039352277
-
The seven-component reaction
-
Doemling, A.; Herdtweck, E.; Ugi, I. The seven-component reaction. Acta Chem. Scand. 1998, 52, 107-113.
-
(1998)
Acta Chem. Scand.
, vol.52
, pp. 107-113
-
-
Doemling, A.1
Herdtweck, E.2
Ugi, I.3
-
16
-
-
70349912163
-
The efficient one-pot reaction of up to eight compo-nents by the union of multicomponent reactions
-
Elders, N.; van der Born, D.; Hendrickx, L.J.D.; Timmer, B.J.J.; Krause, A.; Janssen, E.; de Kanter, F.J.J.; Ruijter, E.; Orru, R.V.A. The efficient one-pot reaction of up to eight compo-nents by the union of multicomponent reactions. Angew. Chem. Int. Ed. Engl. 2009, 48, 5856-5859.
-
(2009)
Angew. Chem. Int. Ed. Engl.
, vol.48
, pp. 5856-5859
-
-
Elders, N.1
Van Der Born, D.2
Hendrickx, L.J.D.3
Timmer, B.J.J.4
Krause, A.5
Janssen, E.6
De Kanter, F.J.J.7
Ruijter, E.8
Orru, R.V.A.9
-
17
-
-
34250627489
-
Multi-component syntheses of heterocycles by transiton-metal catalysis
-
D'Souza, D.M.; Mueller, T.J.J. Multi-component syntheses of heterocycles by transiton-metal catalysis. Chem. Soc. Rev. 2007, 36, 1095-1108.
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1095-1108
-
-
D'Souza, D.M.1
Mueller, T.J.J.2
-
18
-
-
0037079610
-
Multi-component reactions and evolutionary chemistry
-
Weber, L. Multi-component reactions and evolutionary chemistry. Drug Discov. Today 2002, 7, 143-147.
-
(2002)
Drug Discov. Today
, vol.7
, pp. 143-147
-
-
Weber, L.1
-
19
-
-
70349156384
-
Natural product synthesis using multicomponent reaction strategies
-
Toure, B.B.; Hall, D.G. Natural product synthesis using multicomponent reaction strategies. Chem. Rev. 2009, 109, 4439-4486.
-
(2009)
Chem. Rev.
, vol.109
, pp. 4439-4486
-
-
Toure, B.B.1
Hall, D.G.2
-
20
-
-
65249100749
-
Strategies for innovation in multicomponent reaction design
-
Ganem, B. Strategies for innovation in multicomponent reaction design. Acc. Chem. Res. 2009, 42, 463-472.
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 463-472
-
-
Ganem, B.1
-
21
-
-
67650735929
-
Recent progress in three-component reactions. An update
-
Syamala, M. Recent progress in three-component reactions. An update. Org. Prep. Proced. Int. 2009, 4, 1-68.
-
(2009)
Org. Prep. Proced. Int.
, vol.4
, pp. 1-68
-
-
Syamala, M.1
-
22
-
-
78650177928
-
On the industrial applications of MCRs: Molecular diversity in drug discovery and generic drug synthesis
-
Kalinski, C.; Umkehrer, M.; Weber, L.; Kolb, J.; Burdack, C.; Ross, G. On the industrial applications of MCRs: Molecular diversity in drug discovery and generic drug synthesis. Mol. Divers. 2010, 14, 513-522.
-
(2010)
Mol. Divers.
, vol.14
, pp. 513-522
-
-
Kalinski, C.1
Umkehrer, M.2
Weber, L.3
Kolb, J.4
Burdack, C.5
Ross, G.6
-
23
-
-
77952542304
-
Recent advances in multicomponent reactions for diversity-oriented synthesis
-
Biggs-Houck, J.E.; Younai, A.; Shaw, J.T. Recent advances in multicomponent reactions for diversity-oriented synthesis. Curr. Opin. Chem. Biol. 2010, 14, 371-382.
-
(2010)
Curr. Opin. Chem. Biol.
, vol.14
, pp. 371-382
-
-
Biggs-Houck, J.E.1
Younai, A.2
Shaw, J.T.3
-
24
-
-
78349257436
-
Multicomponent reactions for the synthesis of heterocycles
-
Jiang, B.; Rajale, T.; Wever, W.; Tu, S.-J.; Li, G. Multicomponent reactions for the synthesis of heterocycles. Chem. Asian J. 2010, 5, 2318-2335.
-
(2010)
Chem. Asian J.
, vol.5
, pp. 2318-2335
-
-
Jiang, B.1
Rajale, T.2
Wever, W.3
Tu, S.-J.4
Li, G.5
-
25
-
-
79959907066
-
Multicomponent reaction design in the quest for molecular complexity and diversity
-
Ruijter, E.; Scheffelaar, R.; Orru, R.V.A. Multicomponent reaction design in the quest for molecular complexity and diversity. Angew. Chem. Int. Ed. Engl. 2011, 50, 6234-6246.
-
(2011)
Angew. Chem. Int. Ed. Engl.
, vol.50
, pp. 6234-6246
-
-
Ruijter, E.1
Scheffelaar, R.2
Orru, R.V.A.3
-
26
-
-
81255211335
-
Bronsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles
-
Yu, J.; Shit, F.; Gong, L.-Z. Bronsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles. Acc. Chem. Res. 2011, 44, 1156-1171.
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 1156-1171
-
-
Yu, J.1
Shit, F.2
Gong, L.-Z.3
-
27
-
-
33745795313
-
A new highly convergent entry to densely functionalized aziridines based on the Ugi reaction
-
DOI 10.1002/qsar.200540192
-
Banfi, L.; Bossio, A.; Guanti, G.; Paravidino, M.; Riva, R. A new highly convergent entry to densely functionalized aziridines based on the Ugi reaction. QSAR Comb. Sci. 2006, 5-6, 457-460. (Pubitemid 44022722)
-
(2006)
QSAR and Combinatorial Science
, vol.25
, Issue.5-6
, pp. 457-460
-
-
Banfi, L.1
Basso, A.2
Guanti, G.3
Paravidino, M.4
Riva, R.5
-
28
-
-
47349130002
-
Synthesis and synthetic applications of a-amino ketones derived from natural a-amino acids
-
Concellon, J.M.; Rodriguez-Solla, H. Synthesis and synthetic applications of a-amino ketones derived from natural a-amino acids. Curr. Org. Chem. 2008, 12, 524-543.
-
(2008)
Curr. Org. Chem.
, vol.12
, pp. 524-543
-
-
Concellon, J.M.1
Rodriguez-Solla, H.2
-
29
-
-
51149113750
-
Sulfur ylide mediated three-component aziridination and epoxidation reactions using vinyl sulfonium salts
-
Krokotos, C.G.; McGarrigle, E.M.; Aggerwal, V.K.; Varinder, K. Sulfur ylide mediated three-component aziridination and epoxidation reactions using vinyl sulfonium salts. Synlett 2008, 2008, 2191-2195.
-
(2008)
Synlett
, vol.2008
, pp. 2191-2195
-
-
Krokotos, C.G.1
McGarrigle, E.M.2
Aggerwal, V.K.3
Varinder, K.4
-
30
-
-
18244385723
-
Synthesis of cytotoxic derivatives of 2-oxo-1-acetidinylacetamid
-
Veinberg, G.; Diskovskaya, K.; Vorona, M.; Turkovskis, I.; Kanepe, I.; Lukevics, I. Synthesis of cytotoxic derivatives of 2-oxo-1-acetidinylacetamid. Chem. Heterocycl. Compd. 2005, 41, 93-97.
-
(2005)
Chem. Heterocycl. Compd.
, vol.41
, pp. 93-97
-
-
Veinberg, G.1
Diskovskaya, K.2
Vorona, M.3
Turkovskis, I.4
Kanepe, I.5
Lukevics, I.6
-
31
-
-
85014625574
-
The role of isocyanides in the synthesis of β-lactam antibiotics and related compounds
-
Atta-ur-Rahman, Ed.; Elsevier: New York, NY, USA
-
Eckert, H.; Ugi, I. The role of isocyanides in the synthesis of β-lactam antibiotics and related compounds. In Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed.; Elsevier: New York, NY, USA, 1993; pp. 113-143.
-
(1993)
Studies in Natural Products Chemistry
, pp. 113-143
-
-
Eckert, H.1
Ugi, I.2
-
32
-
-
69249205543
-
Two-and three-component reactions leading to new enamines derived from 2,3-dicyanobut-2-enoates
-
Mloston, G.; Celeda, M.; Linden, A.; Heimgartner, H. Two-and three-component reactions leading to new enamines derived from 2,3-dicyanobut-2-enoates. Helv. Chim. Acta 2009, 92, 1520-1537.
-
(2009)
Helv. Chim. Acta
, vol.92
, pp. 1520-1537
-
-
Mloston, G.1
Celeda, M.2
Linden, A.3
Heimgartner, H.4
-
33
-
-
58249096347
-
Solvent-free synthesis of penta-substituted pyrroles: One-pot reaction of amine, alkyl acetoacetate, and fumaryl chloride
-
Alizadeh, A.; Babaki, M.; Zoreh, N. Solvent-free synthesis of penta-substituted pyrroles: one-pot reaction of amine, alkyl acetoacetate, and fumaryl chloride. Tetrahedron 2009, 65, 1704-1707.
-
(2009)
Tetrahedron
, vol.65
, pp. 1704-1707
-
-
Alizadeh, A.1
Babaki, M.2
Zoreh, N.3
-
34
-
-
79953898169
-
Synthesis of functionalized pyrroles via catalyst-and solvent-free sequential three-component enamine-azoene annulations
-
Attanasi, O.A.; Favi, G.; Mantellini, F.; Moscatelli, G.; Santeusanio, S. Synthesis of functionalized pyrroles via catalyst-and solvent-free sequential three-component enamine-azoene annulations. J. Org. Chem. 2011, 76, 2860-2866.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 2860-2866
-
-
Attanasi, O.A.1
Favi, G.2
Mantellini, F.3
Moscatelli, G.4
Santeusanio, S.5
-
35
-
-
53149137500
-
One-pot four-component synthesis of tetra-substituted pyrroles
-
Kassaee, M.Z.; Masrouri, M.; Partiovi, T. One-pot four-component synthesis of tetra-substituted pyrroles. Helv. Chim. Acta 2008, 91, 227-231.
-
(2008)
Helv. Chim. Acta
, vol.91
, pp. 227-231
-
-
Kassaee, M.Z.1
Masrouri, M.2
Partiovi, T.3
-
36
-
-
79953319049
-
Synthesis of cyano-2,3-dihydropyrrolo[1,2-f]phenanthridine derivatives via a domino-Knoevenagel-cyclization
-
Marandi, G.; Maghsoodlou, M.T.; Hazeri, N.; Habibi-Khorassani, S.M.; Torbati, N.A.; Charati, F.R.; Skelton, B.W.; Makha, M. Synthesis of cyano-2,3-dihydropyrrolo[1,2-f]phenanthridine derivatives via a domino-Knoevenagel-cyclization. Mol. Divers. 2011, 15, 197-201.
-
(2011)
Mol. Divers.
, vol.15
, pp. 197-201
-
-
Marandi, G.1
Maghsoodlou, M.T.2
Hazeri, N.3
Habibi-Khorassani, S.M.4
Torbati, N.A.5
Charati, F.R.6
Skelton, B.W.7
Makha, M.8
-
37
-
-
48349102069
-
Three component, highly diastereoselective metal free synthesis of 2,3,4,5 tetrasubstituted pyrrolidines
-
Crovetto, L.; Rios, R. Three component, highly diastereoselective metal free synthesis of 2,3,4,5 tetrasubstituted pyrrolidines. Synlett 2008, 2008, 1840-1844.
-
(2008)
Synlett
, vol.2008
, pp. 1840-1844
-
-
Crovetto, L.1
Rios, R.2
-
38
-
-
28844498979
-
Asymmetric synthesis of multifunctionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reaction
-
DOI 10.1021/ol050819n
-
Xu, H.-W.; Li, G.-Y.; Wong, M.-K.; Che, C.-M. Asymmetric synthesis of multi-functionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reaction. Org. Lett. 2005, 7, 5349-5352. (Pubitemid 41775129)
-
(2005)
Organic Letters
, vol.7
, Issue.24
, pp. 5349-5352
-
-
Xu, H.-W.1
Li, G.-Y.2
Wong, M.-K.3
Che, C.-M.4
-
39
-
-
11144250168
-
Pyrrole syntheses by multicomponent coupling reactions
-
Balme, B. Pyrrole syntheses by multicomponent coupling reactions. Angew. Chem. Int. Ed. Engl. 2004, 43, 6238-6241.
-
(2004)
Angew. Chem. Int. Ed. Engl.
, vol.43
, pp. 6238-6241
-
-
Balme, B.1
-
40
-
-
0037015447
-
One-step synthesis of 3-aryl-and 3,4-diaryl-(1H)-pyrroles using tosylmethyl isocyanide (TOSMIC)
-
Smith, N.D.; Huang, D.; Cosford, N.D.P. One-step synthesis of 3-aryl-and 3,4-diaryl-(1H)-pyrroles using tosylmethyl isocyanide (TOSMIC). Org. Lett. 2002, 4, 3537-3539.
-
(2002)
Org. Lett.
, vol.4
, pp. 3537-3539
-
-
Smith, N.D.1
Huang, D.2
Cosford, N.D.P.3
-
41
-
-
79957992501
-
A straightforward one-pot multicomponent synthesis of polysubstituted pyrroles
-
Lin, X.; Mao, Z.; Dai, X.; Lu, P.; Wang, Y. A straightforward one-pot multicomponent synthesis of polysubstituted pyrroles. Chem. Commun. 2011, 47, 6620-6622.
-
(2011)
Chem. Commun.
, vol.47
, pp. 6620-6622
-
-
Lin, X.1
Mao, Z.2
Dai, X.3
Lu, P.4
Wang, Y.5
-
42
-
-
80052258158
-
Three-component synthesis of poly-substituted pyrroles from a-diazoketones, nitroalkenes, and amines
-
Hong, D.; Zhu, Y.; Li, Y.; Lin, X.; Lu, P.; Wang, Y. Three-component synthesis of poly-substituted pyrroles from a-diazoketones, nitroalkenes, and amines. Org. Lett. 2011, 13, 4668-4671.
-
(2011)
Org. Lett.
, vol.13
, pp. 4668-4671
-
-
Hong, D.1
Zhu, Y.2
Li, Y.3
Lin, X.4
Lu, P.5
Wang, Y.6
-
43
-
-
77956524122
-
Multicomponent reactions for the synthesis of pyrroles
-
Estevez, V.; Villacampa, M.; Menendez, J.J. Multicomponent reactions for the synthesis of pyrroles. Chem. Soc. Rev. 2010, 39, 4402-4421.
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 4402-4421
-
-
Estevez, V.1
Villacampa, M.2
Menendez, J.J.3
-
44
-
-
45249110918
-
3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: A novel binucleophilic system for three-component synthesis of 2-aminofurans
-
DOI 10.1055/s-2008-1067028
-
Alizadeh, A.; Rostamnia, S.; Zhu, L.G. Competition of the R3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: A novel binucleo-philic system for three-component synthesis of 2-aminofurans. Synthesis 2008, 2008, 1788-1792. (Pubitemid 351839137)
-
(2008)
Synthesis
, Issue.11
, pp. 1788-1792
-
-
Alizadeh, A.1
Rostamnia, S.2
Zhu, L.-G.3
-
45
-
-
63349101717
-
New domino approach for the synthesis of 2,3-disubstituted benzo[b]furans via copper-catalyzed multi-component coupling reactions followed by cyclization
-
Li, H.; Li, J.; Yan, B.; Li, Y. New domino approach for the synthesis of 2,3-disubstituted benzo[b]furans via copper-catalyzed multi-component coupling reactions followed by cyclization. Tetrahedron Lett. 2009, 50, 2353-2357.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2353-2357
-
-
Li, H.1
Li, J.2
Yan, B.3
Li, Y.4
-
46
-
-
77957157113
-
Multicomponent reaction of imidazo[1,5-α]pyridine carbenes with aldehydes and dimethyl acetylenedicarboxylate or allenoates: A straightforward approach to fully substituted furans
-
Pan, H.-R.; Li, Y.-J.; Yan, C.-X.; Xing, J.; Cheng, Y. Multicomponent reaction of imidazo[1,5-α]pyridine carbenes with aldehydes and dimethyl acetylenedicarboxylate or allenoates: A straightforward approach to fully substituted furans. J. Org. Chem. 2010, 75, 6644-6652.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 6644-6652
-
-
Pan, H.-R.1
Li, Y.-J.2
Yan, C.-X.3
Xing, J.4
Cheng, Y.5
-
47
-
-
44049106347
-
Microwave-assisted synthesis of N-sec- and N-tert-alkylated indoles
-
DOI 10.1055/s-2008-1067005, T17807SS
-
Schirok, H. Microwave-assisted synthesis of N-sec-and N-tert-alkylated indoles. Synthesis 2008, 2008, 1404-1414. (Pubitemid 351709857)
-
(2008)
Synthesis
, Issue.9
, pp. 1404-1414
-
-
Schirok, H.1
-
48
-
-
27444431741
-
Multiple component Fischer indole reactions
-
DOI 10.1016/j.tet.2005.08.062, PII S0040402005014584, Multicomponent Reactions
-
Simoneau, C.A.; Ganem, B. Multiple component Fischer indole reactions. Tetrahedron 2005, 61, 11374-11379. (Pubitemid 41532306)
-
(2005)
Tetrahedron
, vol.61
, Issue.48
, pp. 11374-11379
-
-
Simoneau, C.A.1
Ganem, B.2
-
49
-
-
38049001929
-
One-pot multicomponent synthesis of indoles from 2-iodobenzoic acid
-
Leogane, O.; Lebel, H. One-pot multicomponent synthesis of indoles from 2-iodobenzoic acid. Angew. Chem. Int. Ed. Engl. 2008, 47, 350-352.
-
(2008)
Angew. Chem. Int. Ed. Engl.
, vol.47
, pp. 350-352
-
-
Leogane, O.1
Lebel, H.2
-
50
-
-
33744519893
-
A novel one-pot synthesis of highly diverse indole scaffolds by the Ugi/Heck reaction
-
DOI 10.1016/j.tetlet.2006.04.127, PII S0040403906008707
-
Kalinski, C.; Umkehrer, M.; Schmidt, J.; Ross, G.; Kolb, J.; Burdack, C.; Hiller, W.; Hoffmann, S.D. A novel one-pot synthesis of highly diverse indole scaffolds by the Ugi/Heck reaction. Tetrahedron Lett. 2006, 47, 4683-4686. (Pubitemid 43815480)
-
(2006)
Tetrahedron Letters
, vol.47
, Issue.27
, pp. 4683-4686
-
-
Kalinski, C.1
Umkehrer, M.2
Schmidt, J.3
Ross, G.4
Kolb, J.5
Burdack, C.6
Hiller, W.7
Hoffmann, S.D.8
-
51
-
-
58149341296
-
A novel one-pot, three-component synthesis of dialkyl 5-(alkylamino)-1-aryl-1H-pyrazole-3,4-dicarboxylates
-
Adib, M.; Mohammadi, B.; Bijanzadeh, H.R. A novel one-pot, three-component synthesis of dialkyl 5-(alkylamino)-1-aryl-1H-pyrazole-3,4- dicarboxylates. Synlett 2008, 2008, 3180-3182.
-
(2008)
Synlett
, vol.2008
, pp. 3180-3182
-
-
Adib, M.1
Mohammadi, B.2
Bijanzadeh, H.R.3
-
52
-
-
79751536505
-
A novel and environment-friendly method for preparing dihydropyrano[2,3-c]pyrazoles in water under ultrasound irradiation
-
Zou, Y.; Wu, H.; Hu, Y.; Liu, H.; Zhao, X.; Ji, H.; Shi, D. A novel and environment-friendly method for preparing dihydropyrano[2,3-c]pyrazoles in water under ultrasound irradiation. Ultrason. Sonochem. 2011, 18, 708-712.
-
(2011)
Ultrason. Sonochem.
, vol.18
, pp. 708-712
-
-
Zou, Y.1
Wu, H.2
Hu, Y.3
Liu, H.4
Zhao, X.5
Ji, H.6
Shi, D.7
-
53
-
-
0141519171
-
A combinatorial scaffold approach based upon a multicomponent reaction
-
DOI 10.1021/ol0343313
-
Bertozzi, F.; Gundersen, B.V.; Gustavsson, M.; Olson, R. A combinatorial scaffold approach based upon a multicomponent reaction. Org. Lett. 2003, 5, 1551-1554. (Pubitemid 37140999)
-
(2003)
Organic Letters
, vol.5
, Issue.9
, pp. 1551-1554
-
-
Bertozzi, F.1
Gundersen, B.V.2
Gustafsson, M.3
Olsson, R.4
-
54
-
-
0037043209
-
Facile two-pot syntheses of novel alternating benzene/imidazole systems
-
DOI 10.1016/S0040-4020(02)00550-1, PII S0040402002005501
-
Sung, K.; Wu, S.H.; Chen, P.I. Facile two-pot syntheses of novel alternating benzene/imidazole systems. Tetrahedron 2002, 58, 5599-5602. (Pubitemid 34722896)
-
(2002)
Tetrahedron
, vol.58
, Issue.28
, pp. 5599-5602
-
-
Sung, K.1
Wu, S.-H.2
Chen, P.-I.3
-
55
-
-
37649024182
-
Highly efficient, four component, one-pot synthesis of tetrasubstituted imidazoles using a catalytic amount of FeCl3x6H2O
-
Heravi, M.M.; Derikwand, F.; Haghighi, M. Highly efficient, four component, one-pot synthesis of tetrasubstituted imidazoles using a catalytic amount of FeCl3x6H2O. Monatsh. Chem. Chem. Mon. 2008, 139, 31-33.
-
(2008)
Monatsh. Chem. Chem. Mon.
, vol.139
, pp. 31-33
-
-
Heravi, M.M.1
Derikwand, F.2
Haghighi, M.3
-
56
-
-
38349191130
-
Synthesis of highly substituted 2-imidazolines through a three-component coupling reaction
-
Han, Y.; Xie, Y.-X.; Zhao, L.-B.; Fan, M.-J.; Liang, Y.-M. Synthesis of highly substituted 2-imidazolines through a three-component coupling reaction. Synthesis 2008, 2008, 87-93.
-
(2008)
Synthesis
, vol.2008
, pp. 87-93
-
-
Han, Y.1
Xie, Y.-X.2
Zhao, L.-B.3
Fan, M.-J.4
Liang, Y.-M.5
-
57
-
-
0034629166
-
An investigation of imidazole and oxazole syntheses using aryl- substituted TosMIC reagents
-
DOI 10.1021/jo991782l
-
Sisko, J.; Kanick, A.J.; Mellinger, M.; Filan, J.F.; Allen, A.; Olsen, M.A. An investigation of imidazole and oxazole syntheses using aryl-substituted TosMIC reagents. J. Org. Chem. 2000, 65, 1516-1524. (Pubitemid 30145985)
-
(2000)
Journal of Organic Chemistry
, vol.65
, Issue.5
, pp. 1516-1524
-
-
Sisko, J.1
Kassick, A.J.2
Mellinger, M.3
Filan, J.J.4
Allen, A.5
Olsen, M.A.6
-
58
-
-
78149304818
-
Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide
-
Hasaninejad, A.; Zare, A.; Shekouhy, M.; Rad, J.A. Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide. J. Comb. Chem. 2010, 12, 844-849.
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 844-849
-
-
Hasaninejad, A.1
Zare, A.2
Shekouhy, M.3
Rad, J.A.4
-
59
-
-
79951484035
-
Carbon-based solid acid as an efficient and reusable catalyst for one-pot synthesis of tetrasubstituted imidazoles under solvent-free conditions
-
Tavakoli-Hoseini, N.; Davoodnia, A. Carbon-based solid acid as an efficient and reusable catalyst for one-pot synthesis of tetrasubstituted imidazoles under solvent-free conditions. Chinese J. Chem. 2011, 29, 203-206.
-
(2011)
Chinese J. Chem.
, vol.29
, pp. 203-206
-
-
Tavakoli-Hoseini, N.1
Davoodnia, A.2
-
60
-
-
34250831544
-
Double insertion of isocyanides into dihydropyridines: Direct access to substituted benzimidazolium salts
-
DOI 10.1002/anie.200605070
-
Masdeu, C.; Gomez, E.; Williams, N.A.O.; Lavilla, R. Double insertion of isocyanides into dihydropyridines: Direct access to substituted benzimidazolium salts. Angew. Chem. Int. Ed. Engl. 2007, 46, 3043-3046. (Pubitemid 46973514)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.17
, pp. 3043-3046
-
-
Masdeu, C.1
Gomez, E.2
Williams, N.A.O.3
Lavilla, R.4
-
61
-
-
60849121072
-
Multicomponent access to functionalized mesoionic structures based on TFAA activation of isocyanides: Novel domino reactions
-
Arevalo, M.J.; Kielland, N.; Masdeu, C.; Miguel, M.; Isambert, N.; Lavilla, R. Multicomponent access to functionalized mesoionic structures based on TFAA activation of isocyanides: Novel domino reactions. Eur. J. Org. Chem. 2009, 617-625.
-
(2009)
Eur. J. Org. Chem.
, pp. 617-625
-
-
Arevalo, M.J.1
Kielland, N.2
Masdeu, C.3
Miguel, M.4
Isambert, N.5
Lavilla, R.6
-
62
-
-
53849109164
-
Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide
-
Yoo, W.-J.; Li, C.-J. Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide. Adv. Synth. Catal. 2008, 350, 1503-1506.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1503-1506
-
-
Yoo, W.-J.1
Li, C.-J.2
-
63
-
-
78651447556
-
Exploiting the divergent reactivity of a-isocyanoacetate: Multicomponent synthesis of 5-alkoxyoxazoles and related heterocycles
-
Lalli, C.; Bouma, M.J.; Bonne, D.; Masson, G.; Zhu, J. Exploiting the divergent reactivity of a-isocyanoacetate: Multicomponent synthesis of 5-alkoxyoxazoles and related heterocycles. Chem. Eur. J. 2011, 17, 880-889.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 880-889
-
-
Lalli, C.1
Bouma, M.J.2
Bonne, D.3
Masson, G.4
Zhu, J.5
-
64
-
-
0345871007
-
New MCRs: The first 4-component reaction leading to 2,4-disubstituted thiazoles
-
DOI 10.1023/B:MODI.0000006827.35029.e4
-
Kolb, J.; Beck, B.; Almstetter, M.; Heck, S.; Herdtweck, E.; Doemling, A. New MCRs: The first 4-component reaction leading to 2,4-disubstituted thiazoles. Mol. Divers. 2003, 6, 297-313. (Pubitemid 38089868)
-
(2003)
Molecular Diversity
, vol.6
, Issue.3-4
, pp. 297-313
-
-
Kolb, J.1
Beck, B.2
Almstetter, M.3
Heck, S.4
Herdtweck, E.5
Domling, A.6
-
65
-
-
11844289672
-
2,4,5-Trisubstituted thiazole building blocks by a novel multi-component reaction
-
DOI 10.1055/s-2004-836035, G37904ST
-
Umkehrer, M.; Kolb, J.; Burdack, C.; Hiller, W. 2,4,5-Trisubstituted thiazole building blocks by a novel multi-component reaction. Synlett 2005, 2005, 79-82. (Pubitemid 40094888)
-
(2005)
Synlett
, Issue.1
, pp. 79-82
-
-
Umkehrer, M.1
Kolb, J.2
Burdack, C.3
Hiller, W.4
-
66
-
-
80052703052
-
Novel application of a-azido aldehydes in multicomponent reactions: Synthesis of triazolo-fused dihydrooxazinones via a passerini reaction-dipolar cycloaddition strategy
-
de Moliner, F.; Crosignani, S.; Galatini, A.; Riva, R.; Basso, A. Novel application of a-azido aldehydes in multicomponent reactions: Synthesis of triazolo-fused dihydrooxazinones via a passerini reaction-dipolar cycloaddition strategy. ACS Comb. Sci. 2011, 13, 453-457.
-
(2011)
ACS Comb. Sci.
, vol.13
, pp. 453-457
-
-
De Moliner, F.1
Crosignani, S.2
Galatini, A.3
Riva, R.4
Basso, A.5
-
67
-
-
5644259644
-
A versatile synthesis of fused triazolo derivatives by sequential Ugi/alkyne-azide cycloaddition reactions
-
DOI 10.1016/j.tetlet.2004.09.117, PII S0040403904020854
-
Akritopoulou-Zanze, I.; Gracias, V.; Djuric, S.W. A versatile synthesis of fused triazolo derivatives by sequential Ugi/alkyne-azide cycloaddition reactions. Tetrahedron Lett. 2004, 45, 8439-8441. (Pubitemid 39369885)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.46
, pp. 8439-8441
-
-
Akritopoulou-Zanze, I.1
Gracias, V.2
Djuric, S.W.3
-
68
-
-
79952120925
-
A copper(I) isonitrile complex as a heterogeneous catalyst for azide-alkyne cycloaddition in water
-
Liu, M.; Reiser, O. A copper(I) isonitrile complex as a heterogeneous catalyst for azide-alkyne cycloaddition in water. Org. Lett. 2011, 13, 1102-1105.
-
(2011)
Org. Lett.
, vol.13
, pp. 1102-1105
-
-
Liu, M.1
Reiser, O.2
-
69
-
-
33746210083
-
Inhibitors of HIV-1 protease by using in situ click chemistry
-
DOI 10.1002/anie.200502161
-
Whiting, M.; Muldroon, J.; Silverman, S.M.; Lindstrom, W.; Olson, A.J.; Kolb, H.C.; Finn, M.G.; Sharpless, K.B.; Elder, J.H.; Fokin, V.V. Inhibitors of HIV-1 protease by using in situ click chemistry. Angew. Chem. Int. Ed. Engl. 2006, 45, 1435-1439. (Pubitemid 44097627)
-
(2006)
Angewandte Chemie - International Edition
, vol.45
, Issue.9
, pp. 1435-1439
-
-
Whiting, M.1
Muldoon, J.2
Lin, Y.-C.3
Silverman, S.M.4
Lindstrom, W.5
Olson, A.J.6
Kolb, H.C.7
Finn, M.G.8
Sharpless, K.B.9
Elder, J.H.10
Fokin, V.V.11
-
70
-
-
43449108552
-
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 Deliv. Rev. 2008, 60, 958-970.
-
(2008)
Adv. Drug Deliv. Rev.
, vol.60
, pp. 958-970
-
-
Lutz, J.F.1
Zarafshani, Z.2
-
71
-
-
34250353931
-
Click chemistry - What's in a name? Triazole synthesis and beyond
-
DOI 10.1055/s-2007-966071
-
Gil, M.V.; Arevalo, M.J.; Lopez, O. Click chemistry: What's in a name? Triazol synthesis and beyond. Synthesis 2007, 2007, 1589-1620. (Pubitemid 46911512)
-
(2007)
Synthesis
, Issue.11
, pp. 1589-1620
-
-
Gil, M.V.1
Arevalo, M.J.2
Lopez, O.3
-
72
-
-
33845256893
-
Stereoselective synthesis of multifunctionalized 1,2,4-triazolidines by a ruthenium porphyrin-catalyzed three-component coupling reaction
-
DOI 10.1002/adsc.200600320
-
Wang, M.-Z.; Xu, H.-W.; Liu, Y.; Wong, M.-K. Stereoselective synthesis of multi-functionalized 1,2,4-triazolidines by a ruthenium porphyrin-catalyzed three-component coupling reaction. Adv. Synth. Catal. 2006, 348, 2391-2396. (Pubitemid 44865617)
-
(2006)
Advanced Synthesis and Catalysis
, vol.348
, Issue.16-17
, pp. 2391-2396
-
-
Wang, M.-Z.1
Xu, H.-W.2
Liu, Y.3
Wong, M.-K.4
Che, C.-M.5
-
73
-
-
79951633283
-
Rapid synthesis of 1,3,5-substituted 1,2,4-triazoles from carboxylic acids, amidines, and hydrazines
-
Castanedo, G.M.; Seng, P.S.; Blaquiere, N.; Trapp, S.; Staben, S.T. Rapid synthesis of 1,3,5-substituted 1,2,4-triazoles from carboxylic acids, amidines, and hydrazines. J. Org. Chem. 2011, 76, 1177-1179.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 1177-1179
-
-
Castanedo, G.M.1
Seng, P.S.2
Blaquiere, N.3
Trapp, S.4
Staben, S.T.5
-
74
-
-
64249107551
-
Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4- tetrazoles under solvent-free conditions
-
Kundu, D.; Majee, A.; Hajra, A. Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4-tetrazoles under solvent-free conditions. Tetrahedron Lett. 2009, 50, 2668-2670.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2668-2670
-
-
Kundu, D.1
Majee, A.2
Hajra, A.3
-
75
-
-
36549070069
-
Studies on isocyanides: Synthesis of tetrazolyl-isoindolinones via tandem Ugi four-component condensation/intramolecular amidation
-
DOI 10.1016/j.tetlet.2007.10.154, PII S0040403907021636
-
Marcos, C.M.; Marcaccini, S.; Menchi, G.; Pepino, R.; Torroba, T. Studies on isocyanides: Synthesis of tetrazolyl-isoindolinones via tandem Ugi four-component condensation / intramolecular amidation. Tetrahedron Lett. 2008, 49, 149-152. (Pubitemid 350191867)
-
(2008)
Tetrahedron Letters
, vol.49
, Issue.1
, pp. 149-152
-
-
Marcos, C.F.1
Marcaccini, S.2
Menchi, G.3
Pepino, R.4
Torroba, T.5
-
76
-
-
79952157097
-
Three-component strategy toward 5-membered heterocycles from isocyanide dibromides
-
Kaim, L.; Grimaud, L.; Patil, P. Three-component strategy toward 5-membered heterocycles from isocyanide dibromides. Org. Lett. 2011, 13, 1261-1263.
-
(2011)
Org. Lett.
, vol.13
, pp. 1261-1263
-
-
Kaim, L.1
Grimaud, L.2
Patil, P.3
-
77
-
-
0001034439
-
A novel synthetic route to 1,6-dihydro-6-oxopyridine-2-carboxylic acid derivatives
-
Bossio, R.; Marcos, C.F.; Marcaccini, S.; Pepino, R. A novel synthetic route to 1,6-dihydro-6-oxopyridine-2-carboxylic acid derivatives. Heterocycles 1997, 45, 1589-1592.
-
(1997)
Heterocycles
, vol.45
, pp. 1589-1592
-
-
Bossio, R.1
Marcos, C.F.2
Marcaccini, S.3
Pepino, R.4
-
78
-
-
66149157758
-
Synthesis of isoxazolo[5,4-b]pyridines by microwave-assisted multi-component reactions in water
-
Tu, S.-J.; Zhang, X.H.; Han, Z.-G.; Cao, X.D.; Wu, S.-S.; Yan, S.; Hao, W.-J.; Zhang, G.; Ma, N. Synthesis of isoxazolo[5,4-b]pyridines by microwave-assisted multi-component reactions in water. J. Comb. Chem. 2009, 11, 428-432.
-
(2009)
J. Comb. Chem.
, vol.11
, pp. 428-432
-
-
Tu, S.-J.1
Zhang, X.H.2
Han, Z.-G.3
Cao, X.D.4
Wu, S.-S.5
Yan, S.6
Hao, W.-J.7
Zhang, G.8
Ma, N.9
-
79
-
-
80051599854
-
A grinding-induced catalyst-and solvent-free synthesis of highly functionalized 1,4-dihydropyridines via a domino multicomponent reaction
-
Kumar, A.; Sharma, S. A grinding-induced catalyst-and solvent-free synthesis of highly functionalized 1,4-dihydropyridines via a domino multicomponent reaction. Green Chem. 2011, 13, 2017-2020.
-
(2011)
Green Chem.
, vol.13
, pp. 2017-2020
-
-
Kumar, A.1
Sharma, S.2
-
80
-
-
79954421874
-
New four-component reactions in water: A convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,40-pyrazolo[3,4-b] pyridine derivatives
-
Balamurugan, K.; Perumal, S.; Menendez, J.C. New four-component reactions in water: A convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,40-pyrazolo[3,4-b]pyridine derivatives. Tetrahedron 2011, 67, 3201-3208.
-
(2011)
Tetrahedron
, vol.67
, pp. 3201-3208
-
-
Balamurugan, K.1
Perumal, S.2
Menendez, J.C.3
-
81
-
-
66349130441
-
A facile synthesis of furo[3,4-e]pyrazolo[3,4-b]pyridine-5(7H)-one derivatives via three-component reaction in ionic liquid without any catalyst
-
Shi, D.-Q.; Yang, F.; Nib, S.N. A facile synthesis of furo[3,4-e]pyrazolo[3,4-b]pyridine-5(7H)-one derivatives via three-component reaction in ionic liquid without any catalyst. J. Heterocycl. Chem. 2009, 46, 469-476.
-
(2009)
J. Heterocycl. Chem.
, vol.46
, pp. 469-476
-
-
Shi, D.-Q.1
Yang, F.2
Nib, S.N.3
-
82
-
-
77349122549
-
Ionic liquid-promoted multi-component reaction: Novel and efficient preparation of pyrazolo[3,4-b]pyridinone, pyrazolo[3,4-b]-quinolinone and their hybrids with pyrimidine nucleoside
-
Zhang, X.; Li, D.; Fan, X.; Wang, X.; Li, X.; Qu, G.; Wang, J. Ionic liquid-promoted multi-component reaction: novel and efficient preparation of pyrazolo[3,4-b]pyridinone, pyrazolo[3,4-b]-quinolinone and their hybrids with pyrimidine nucleoside. Mol. Divers. 2010, 14, 159-167.
-
(2010)
Mol. Divers.
, vol.14
, pp. 159-167
-
-
Zhang, X.1
Li, D.2
Fan, X.3
Wang, X.4
Li, X.5
Qu, G.6
Wang, J.7
-
83
-
-
79957636776
-
Convenient ultrasound-promoted regioselective synthesis of fused 6-amino-3-methyl-4-aryl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile
-
Zare, L.; Mahmoodi, O.; Yahyazadeh, A.; Mamaghani, M. Convenient ultrasound-promoted regioselective synthesis of fused 6-amino-3-methyl-4-aryl- 1H-pyrazolo[3,4-b]pyridine-5-carbonitrile. Synth. Commun. 2011, 41, 2323-2330.
-
(2011)
Synth. Commun.
, vol.41
, pp. 2323-2330
-
-
Zare, L.1
Mahmoodi, O.2
Yahyazadeh, A.3
Mamaghani, M.4
-
84
-
-
66249101971
-
Synthesis of highly functionalized bis(4H-chromene) and 4H-benzo[g]chromene derivatives via an isocyanide-based pseudo-five-component Reaction
-
Shaabani, A.; Ghadari, R.; Beheshdi, S.; Sarvary, A.; Rezayan, A.H. Synthesis of highly functionalized bis(4H-chromene) and 4H-benzo[g]chromene derivatives via an isocyanide-based pseudo-five-component Reaction. J. Org. Chem. 2009, 74, 4372-4374.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4372-4374
-
-
Shaabani, A.1
Ghadari, R.2
Beheshdi, S.3
Sarvary, A.4
Rezayan, A.H.5
-
85
-
-
38849124974
-
Facile synthesis of 3-(aminomethyl)isoquinolines by copper-catalysed domino four-component coupling and cyclisation
-
DOI 10.1039/b718201e
-
Ohta, Y.; Oishi, S.; Fujii, N.; Ohno, H. Facile synthesis of 3-(aminomethyl)isoquinolines by copper-catalysed domino four-component coupling and cyclisation. Chem. Comm. 2008, 835-837. (Pubitemid 351208239)
-
(2008)
Chemical Communications
, Issue.7
, pp. 835-837
-
-
Ohta, Y.1
Oishi, S.2
Fujii, N.3
Ohno, H.4
-
86
-
-
34248584543
-
A novel, one-pot, three-component synthesis of 4H-pyrido[1,2-a] pyrimidines
-
DOI 10.1016/j.tetlet.2007.04.068, PII S0040403907007423
-
Adib, M.; Sayahi, M.-H.; Nosrati, M.; Zhu, L.-G. A novel, one-pot, three-component synthesis of 4H-pyrido[1,2-α]pyrimidines. Tetrahedron Lett. 2007, 48, 4195-4198. (Pubitemid 46754395)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.24
, pp. 4195-4198
-
-
Adib, M.1
Sayahi, M.H.2
Nosrati, M.3
Zhu, L.-G.4
-
87
-
-
77951611528
-
A novel and efficient one-pot synthesis of 2-aminopyrimidinones and their self-assembly
-
Bararjanian, M.; Balalaie, S.; Rominer, F.; Barouti, S. A novel and efficient one-pot synthesis of 2-aminopyrimidinones and their self-assembly. Helv. Chim. Acta 2010, 93, 777-784.
-
(2010)
Helv. Chim. Acta
, vol.93
, pp. 777-784
-
-
Bararjanian, M.1
Balalaie, S.2
Rominer, F.3
Barouti, S.4
-
88
-
-
80052140174
-
One-pot combinatorial synthesis of benzo[4,5]-imidazo-[1,2-α] thiopyrano[3,4-d]pyrimidin-4(3H)-one derivatives
-
Shen, S.; Zhang, H.; Yang, W.; Yu, C.; Yao, C. One-pot combinatorial synthesis of benzo[4,5]-imidazo-[1,2-α]thiopyrano[3,4-d]pyrimidin-4(3H)- one derivatives. Chin. J. Chem. 2011, 29, 1727-1731.
-
(2011)
Chin. J. Chem.
, vol.29
, pp. 1727-1731
-
-
Shen, S.1
Zhang, H.2
Yang, W.3
Yu, C.4
Yao, C.5
-
89
-
-
20044388356
-
One-step construction of peptidomimetic 5-carbamoyl-4-sulfonyl-2- piperazinones
-
Ailyin, A.P.; Trifilenkov, A.S.; Kurashvili, I.D.; Krasavin, M.; Ivachtchenko, A.V. One-step construction of peptidomimetic 5-carbamoyl-4- sulfonyl-2-piperazinones. J. Comb. Chem. 2005, 7, 360-363.
-
(2005)
J. Comb. Chem.
, vol.7
, pp. 360-363
-
-
Ailyin, A.P.1
Trifilenkov, A.S.2
Kurashvili, I.D.3
Krasavin, M.4
Ivachtchenko, A.V.5
-
90
-
-
66149097336
-
Fluorous parallel synthesis of a piperazinedione-fused tricyclic compoundl library
-
Werner, S.; Nielsen, S.D.; Wipf, P.; Turner, D.M.; Chambers, P.G.; Geib, S.J.; Curran, D.P.; Zhang, W. Fluorous parallel synthesis of a piperazinedione-fused tricyclic compoundl library. J. Comb. Chem. 2009, 11, 452-459.
-
(2009)
J. Comb. Chem.
, vol.11
, pp. 452-459
-
-
Werner, S.1
Nielsen, S.D.2
Wipf, P.3
Turner, D.M.4
Chambers, P.G.5
Geib, S.J.6
Curran, D.P.7
Zhang, W.8
-
91
-
-
77956050442
-
Piperazine scaffolds via isocyanide-based multicomponent reactions
-
Domling, A.; Huang, Y. Piperazine scaffolds via isocyanide-based multicomponent reactions. Synthesis 2010, 2010, 2859-2883.
-
(2010)
Synthesis 2010
, pp. 2859-2883
-
-
Domling, A.1
Huang, Y.2
-
92
-
-
75749131130
-
Environmentally safe one-pot solvent-free synthesis of 6-aryl-1,2,4,5-tetrazinane-3 thiones(ones) catalyzed by NaHSO4-SiO2
-
Kanagarajan, V.; Sureshkumar, P.; Thanusu, J.; Gopalakrishnan, M. Environmentally safe one-pot solvent-free synthesis of 6-aryl-1,2,4,5- tetrazinane-3 thiones(ones) catalyzed by NaHSO4-SiO2. Russ. J. Org. Chem. 2009, 45, 1707-1713.
-
(2009)
Russ. J. Org. Chem.
, vol.45
, pp. 1707-1713
-
-
Kanagarajan, V.1
Sureshkumar, P.2
Thanusu, J.3
Gopalakrishnan, M.4
-
93
-
-
77955470708
-
Synthesis of pseudopeptidic (S)-6-amino-5-oxo-1,4-diazepines and (S)-3-benzyl-2-oxo-1,4-benzodiazepines by an Ugi 4CC Staudinger/aza-Wittig sequence
-
Lezinska, P.; Corres, N.; Moreno, D.; Garcia-Valverde, M.; Marcaccini, S.; Torroba, T. Synthesis of pseudopeptidic (S)-6-amino-5-oxo-1,4-diazepines and (S)-3-benzyl-2-oxo-1,4-benzodiazepines by an Ugi 4CC Staudinger/aza-Wittig sequence. Tetrahedron 2010, 66, 6783-6788.
-
(2010)
Tetrahedron
, vol.66
, pp. 6783-6788
-
-
Lezinska, P.1
Corres, N.2
Moreno, D.3
Garcia-Valverde, M.4
Marcaccini, S.5
Torroba, T.6
-
94
-
-
33847681051
-
The reaction of (N-isocyanimino)triphenylphosphorane with dialkyl acetylenedicarboxylates in the presence of 1,3-diphenyl-1,3-propanedione: A novel three-component reaction for the stereoselective synthesis of dialkyl (Z)-2-(5,7-diphenyl-1,3,4-oxadiazepin-2-yl)-2-butenedioates
-
DOI 10.1016/j.tetlet.2007.02.010, PII S0040403907002651
-
Souldozi, A.; Bouslimani, N.; Welter, R. The reaction of (N-isocyanimino)triphenylphos-phorane with dialkyl acetylenedicarboxylates in the presence of 1,3-diphenyl-1,3-propanedione: A novel three-component reaction for the stereoselective synthesis of dialkyl (Z)-2-(5,7-diphenyl-1,3,4- oxadiazepin-2-yl)-2-butenedioates. Tetrahedron Lett. 2007, 48, 2617-2620. (Pubitemid 46356461)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.14
, pp. 2617-2620
-
-
Souldozi, A.1
Ramazani, A.2
Bouslimani, N.3
Welter, R.4
-
95
-
-
33847080427
-
Direct synthesis of pyrroles from Imines, alkynes, and acid chlorides: An isocyanide-mediated reaction
-
Cyr, D.C.; Martin, N.; Arndtsen, B.A. Direct synthesis of pyrroles from Imines, alkynes, and acid chlorides: An isocyanide-mediated reaction. Org. Lett. 2007, 9, 449-452.
-
(2007)
Org. Lett.
, vol.9
, pp. 449-452
-
-
Cyr, D.C.1
Martin, N.2
Arndtsen, B.A.3
-
96
-
-
0034728837
-
A facile synthesis of annelated pyridines from β-formyl enamides under microwave irradiation
-
DOI 10.1016/S0040-4039(00)00405-6, PII S0040403900004056
-
Sharma, U.; Shahadat, A.; Boruah, R.C. A facile synthesis of annelated pyridines from β-formyl enamides under microwave irradiation. Tetrahedron Lett. 2000, 41, 3493-3495. (Pubitemid 30307844)
-
(2000)
Tetrahedron Letters
, vol.41
, Issue.18
, pp. 3493-3495
-
-
Sharma, U.1
Ahmed, S.2
Boruah, R.C.3
-
97
-
-
67650650696
-
Application of malononitrile in multicomponent reactions
-
Wang, Q.; Song, X.; Yan, C. Application of malononitrile in multicomponent reactions. Huaxue Jinzhan 2009, 21, 997-1007.
-
(2009)
Huaxue Jinzhan
, vol.21
, pp. 997-1007
-
-
Wang, Q.1
Song, X.2
Yan, C.3
-
98
-
-
77956591638
-
1,3-Dicarbonyl compounds in stereoselective domino and multicomponent reactions
-
Bonne, D.; Coquerel, Y.; Constantieux, T.; Rodriguez, J. 1,3-Dicarbonyl compounds in stereoselective domino and multicomponent reactions. Tetrahedron: Asymmetry 2010, 21, 1085-1109.
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 1085-1109
-
-
Bonne, D.1
Coquerel, Y.2
Constantieux, T.3
Rodriguez, J.4
-
99
-
-
84856173939
-
β-Diketo building blocks for MCRs-based syntheses of heterocycles
-
Duque, M.; Allais, C.; Isambert, N.; Constantieux, T.; Rodriguez, J. β-Diketo building blocks for MCRs-based syntheses of heterocycles. Top. Heterocycl. Chem. 2010, 23, 227-277.
-
(2010)
Top. Heterocycl. Chem.
, vol.23
, pp. 227-277
-
-
Duque, M.1
Allais, C.2
Isambert, N.3
Constantieux, T.4
Rodriguez, J.5
-
100
-
-
79955772132
-
Recent developments in the reactivity of the Biginelli compounds
-
Matache, M.; Dobrota, C.; Bogdan, N.D.; Funeriu, D.P. Recent developments in the reactivity of the Biginelli compounds. Curr. Org. Synth. 2011, 8, 356-373.
-
(2011)
Curr. Org. Synth.
, vol.8
, pp. 356-373
-
-
Matache, M.1
Dobrota, C.2
Bogdan, N.D.3
Funeriu, D.P.4
-
101
-
-
79956371243
-
Molecular diversity of three-component reactions of aromatic aldehydes, arylamines, and acetylenedicarboxylates
-
Sun, J.; Wu, Q.; Xia, E.-Y.; Yan, C.G. Molecular diversity of three-component reactions of aromatic aldehydes, arylamines, and acetylenedicarboxylates. Eur. J. Org. Chem. 2011, 2011, 2981-2986.
-
(2011)
Eur. J. Org. Chem.
, vol.2011
, pp. 2981-2986
-
-
Sun, J.1
Wu, Q.2
Xia, E.-Y.3
Yan, C.G.4
-
102
-
-
80053053888
-
Recent advances in the chemistry of imine-based multicomponent reactions (MCRs)
-
Choudhury, L.H.; Parvin, T. Recent advances in the chemistry of imine-based multicomponent reactions (MCRs). Tetrahedron 2011, 67, 8213-8228.
-
(2011)
Tetrahedron
, vol.67
, pp. 8213-8228
-
-
Choudhury, L.H.1
Parvin, T.2
-
103
-
-
59949090727
-
Beyond the Ugi reaction: Less conventional interactions between isocyanides and iminium species
-
El Kaim, L.; Grimaud, L. Beyond the Ugi reaction: Less conventional interactions between isocyanides and iminium species. Tetrahedron 2009, 65, 2153-2171.
-
(2009)
Tetrahedron
, vol.65
, pp. 2153-2171
-
-
El Kaim, L.1
Grimaud, L.2
-
104
-
-
78649554190
-
Multi-component reactions of isocyanides in the synthesis of heterocycles
-
Ivachtchenko, A.V.; Ivanenkov, Y.A.; Kysil, V.M.; Krasavin, M.Y.; Ilyin, A.P. Multi-component reactions of isocyanides in the synthesis of heterocycles. Russ. Chem. Rev. 2010, 79, 787-817.
-
(2010)
Russ. Chem. Rev.
, vol.79
, pp. 787-817
-
-
Ivachtchenko, A.V.1
Ivanenkov, Y.A.2
Kysil, V.M.3
Krasavin, M.Y.4
Ilyin, A.P.5
-
105
-
-
79953854104
-
A-Acidic isocyanides in multicomponent chemistry
-
Elders, N.; Ruijter, E.; Nenajdenko, V.G.; Orru, R.V.A. a-Acidic isocyanides in multicomponent chemistry. Top. Heterocycl. Chem. 2010, 23, 129-159.
-
(2010)
Top. Heterocycl. Chem.
, vol.23
, pp. 129-159
-
-
Elders, N.1
Ruijter, E.2
Nenajdenko, V.G.3
Orru, R.V.A.4
-
106
-
-
79952897776
-
Recent application of isocyanides in synthesis of heterocycles
-
Sadjadi, S.; Heravi, M.M. Recent application of isocyanides in synthesis of heterocycles. Tetrahedron 2011, 67, 2707-2752.
-
(2011)
Tetrahedron
, vol.67
, pp. 2707-2752
-
-
Sadjadi, S.1
Heravi, M.M.2
-
107
-
-
79957779724
-
Catalytic multicomponent reactions based on isocyanides
-
Heravi, M.M.; Moghimi, S. Catalytic multicomponent reactions based on isocyanides. J. Iran. Chem. Soc. 2011, 8, 306-373.
-
(2011)
J. Iran. Chem. Soc.
, vol.8
, pp. 306-373
-
-
Heravi, M.M.1
Moghimi, S.2
-
108
-
-
80052426829
-
Beyond Ugi and Passerini reactions. Multicomponent approaches based on isocyanides and alkynes as an efficient tool for diversity oriented synthesis
-
de Moliner, F.; Banfi, L.; Riva, R.; Basso, A. Beyond Ugi and Passerini reactions. Multicomponent approaches based on isocyanides and alkynes as an efficient tool for diversity oriented synthesis. Comb. Chem. High Throughput Screen. 2011, 14, 782-810.
-
(2011)
Comb. Chem. High Throughput Screen.
, vol.14
, pp. 782-810
-
-
De Moliner, F.1
Banfi, L.2
Riva, R.3
Basso, A.4
-
109
-
-
79953294313
-
Recent progress of isocyanide-based multicomponent reactions in Iran
-
Shaabani, A.; Maleki, A.; Rezayan, A.H.; Sarvary, A. Recent progress of isocyanide-based multicomponent reactions in Iran. Mol. Divers. 2011, 15, 41-68.
-
(2011)
Mol. Divers.
, vol.15
, pp. 41-68
-
-
Shaabani, A.1
Maleki, A.2
Rezayan, A.H.3
Sarvary, A.4
-
111
-
-
78649671753
-
Solvent-free and safe process for the quantitative production of phosgene from triphosgene by deactivated imino-based catalysts
-
Eckert, H.; Auerweck, J. Solvent-free and safe process for the quantitative production of phosgene from triphosgene by deactivated imino-based catalysts. Org. Process Res. Dev. 2010, 14, 1501-1505.
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 1501-1505
-
-
Eckert, H.1
Auerweck, J.2
-
112
-
-
84856152821
-
Phosgenation reactions with phosgene from triphosgene
-
Eckert, H. Phosgenation reactions with phosgene from triphosgene. Chim. OGGI 2011, 29, 40-46.
-
(2011)
Chim. OGGI
, vol.29
, pp. 40-46
-
-
Eckert, H.1
-
113
-
-
66249125675
-
Multicomponent reactions of convertible isonitriles
-
Pirrung, M.C.; Ghorai, S.; Ibarra-Rivera, T.R. Multicomponent reactions of convertible isonitriles. J. Org. Chem. 2009, 74, 4110-4117.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4110-4117
-
-
Pirrung, M.C.1
Ghorai, S.2
Ibarra-Rivera, T.R.3
-
114
-
-
84856171807
-
Multicomponent syntheses of macrocycles
-
Masson, G.; Neuville, L.; Bughin, C.; Fayol, A.; Zhu, J. Multicomponent syntheses of macrocycles. Top. Heterocycl. Chem. 2010, 25, 1-24.
-
(2010)
Top. Heterocycl. Chem.
, vol.25
, pp. 1-24
-
-
Masson, G.1
Neuville, L.2
Bughin, C.3
Fayol, A.4
Zhu, J.5
-
115
-
-
63849191356
-
Multiple multicomponent macrocyclisations (MiBs): A strategic development toward macrocycle diversity
-
Wessjohann, L.A.; Rivera, D.G.; Vercillo, O.E. Multiple multicomponent macrocyclisations (MiBs): A strategic development toward macrocycle diversity. Chem. Rev. 2009, 109, 796-814.
-
(2009)
Chem. Rev.
, vol.109
, pp. 796-814
-
-
Wessjohann, L.A.1
Rivera, D.G.2
Vercillo, O.E.3
-
116
-
-
73149096486
-
Multicomponent reactions in water
-
Kumaravel, K.; Vasuki, G. Multicomponent reactions in water. Curr. Org. Chem. 2009, 13, 1820-1841.
-
(2009)
Curr. Org. Chem.
, vol.13
, pp. 1820-1841
-
-
Kumaravel, K.1
Vasuki, G.2
-
117
-
-
79951864858
-
Multicomponent reactions and ionic liquids: A perfect synergy for eco-compatible heterocyclic synthesis
-
Isambert, N.; Duque, M.; del Mar, S.; Plaquevent, J.-C.; Genisson, Y.; Rodriguez, J.; Constantieux, T. Multicomponent reactions and ionic liquids: A perfect synergy for eco-compatible heterocyclic synthesis. Chem. Soc. Rev. 2011, 40, 1347-1357.
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 1347-1357
-
-
Isambert, N.1
Duque, M.2
Del Mar, S.3
Plaquevent, J.-C.4
Genisson, Y.5
Rodriguez, J.6
Constantieux, T.7
-
118
-
-
73849106328
-
Microwave multicomponent synthesis
-
Hugel, H.M. Microwave multicomponent synthesis. Molecules 2009, 14, 4936-4972.
-
(2009)
Molecules
, vol.14
, pp. 4936-4972
-
-
Hugel, H.M.1
-
119
-
-
77952317114
-
Microwave-assisted multicomponent reactions in the heterocyclic chemistry
-
Jiang, B.; Shi, F.; Tu, S.-J. Microwave-assisted multicomponent reactions in the heterocyclic chemistry. Curr. Org. Chem. 2010, 14, 357-378.
-
(2010)
Curr. Org. Chem.
, vol.14
, pp. 357-378
-
-
Jiang, B.1
Shi, F.2
Tu, S.-J.3
-
120
-
-
79961084642
-
Microwave-assisted multicomponent synthesis of heterocycles
-
Kruithof, A.; Ruijter, E.; Orru, R.V.A. Microwave-assisted multicomponent synthesis of heterocycles. Curr. Org. Chem. 2011, 15, 204-236.
-
(2011)
Curr. Org. Chem.
, vol.15
, pp. 204-236
-
-
Kruithof, A.1
Ruijter, E.2
Orru, R.V.A.3
-
121
-
-
79952760490
-
Microwave-assisted fluorous multicomponent reactions. A combinatorial chemistry approach for green organic synthesis
-
Kadam, A.; Zhang, Z.; Zhang, W. Microwave-assisted fluorous multicomponent reactions. A combinatorial chemistry approach for green organic synthesis. Curr. Org. Synth. 2011, 8, 295-309.
-
(2011)
Curr. Org. Synth.
, vol.8
, pp. 295-309
-
-
Kadam, A.1
Zhang, Z.2
Zhang, W.3
-
122
-
-
77954770357
-
Infrared irradiation: An alternative for reaction activation and its contribution to green chemistry
-
Miranda, R.; Noguez, O.; Velasco, B.; Arroyo, G.; Penieres, G.; Martinez, J.O.; Delgado, F. Infrared irradiation: An alternative for reaction activation and its contribution to green chemistry. Educ. Quim. 2009, 20, 421-425.
-
(2009)
Educ. Quim.
, vol.20
, pp. 421-425
-
-
Miranda, R.1
Noguez, O.2
Velasco, B.3
Arroyo, G.4
Penieres, G.5
Martinez, J.O.6
Delgado, F.7
|