-
1
-
-
84955394357
-
-
Yamamoto, H. (Ed) Wiley: Weinheim
-
Yamamoto, H. (Ed). Lewis Acids in Organic Synthesis; Wiley: Weinheim, 2000; vols. 1 and 2.
-
(2000)
Lewis Acids in Organic Synthesis
, vol.1-2
-
-
-
4
-
-
0036625262
-
Rare-earth metal triflates in organic synthesis
-
Kobayashi, S.; Sugiura, M.; Kitagawa, H.; Lam, W. L. Rare-earth metal triflates in organic synthesis. Chem. Rev. 2002, 102, 2227.
-
(2002)
Chem. Rev.
, vol.102
, pp. 2227
-
-
Kobayashi, S.1
Sugiura, M.2
Kitagawa, H.3
Lam, W.L.4
-
5
-
-
0001008984
-
Use of lanthanide(III) ions as catalysts for the reactions of amines with nitriles
-
Forsberg, J. H.; Spaziano, V. T.; Balasubramanian, T. M.; Liu, G. K.; Kinsley, S. A.; Duckworth, C. A.; Poteruca, J. J.; Brown, P. S.; Miller, J. L. Use of lanthanide(III) ions as catalysts for the reactions of amines with nitriles. J. Org. Chem. 1987, 52, 1017.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 1017
-
-
Forsberg, J.H.1
Spaziano, V.T.2
Balasubramanian, T.M.3
Liu, G.K.4
Kinsley, S.A.5
Duckworth, C.A.6
Poteruca, J.J.7
Brown, P.S.8
Miller, J.L.9
-
8
-
-
0033490799
-
Characterization, and anticonvulsant activity of enaminones, part 6: Synthesis of substituted vinylic benzamides as potential anticonvulsants
-
Foster, J. E.; Nicholson, J. M.; Butcher, R.; Stables, J. P.; Edafiogho, I. O.; Goodwin, A. M.; Henson, M. C.; Smith, C. A.; Scott, K. R. Synthesis, characterization, and anticonvulsant activity of enaminones, part 6: Synthesis of substituted vinylic benzamides as potential anticonvulsants. Bioorg. Med. Chem. 1999, 7, 2415
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 2415
-
-
Foster, J.E.1
Nicholson, J.M.2
Butcher, R.3
Stables, J.P.4
Edafiogho, I.O.5
Goodwin, A.M.6
Henson, M.C.7
Smith, C.A.8
Synthesis, R.S.K.9
-
9
-
-
0141974909
-
Traceless solid phase synthesis of 2-substituted pyrimidines using an ''off-the-shelf'' chlorogermane-functionalised resin
-
Spivey, A. C.; Srikaran, R.; Diaper, C. M.; Turner, D. J. Traceless solid phase synthesis of 2-substituted pyrimidines using an ''off-the-shelf'' chlorogermane-functionalised resin. Org. Biomol. Chem. 2003, 1, 1638
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 1638
-
-
Spivey, A.C.1
Srikaran, R.2
Diaper, C.M.3
Turner, D.J.4
-
10
-
-
0028003718
-
And diaster-eoselective reduction of b-enamino esters: A convenient synthesis of both cis-and trans-c-amino alcohols and b-amino esters
-
Bartoli, G.; Cimarelli, C.; Marcantoni, E.; Palmieri, G.; Petrini, M. Chemo-and diaster-eoselective reduction of b-enamino esters: A convenient synthesis of both cis-and trans-c-amino alcohols and b-amino esters. J. Org. Chem. 1994, 59, 5328
-
(1994)
J. Org. Chem.
, vol.59
, pp. 5328
-
-
Bartoli, G.1
Cimarelli, C.2
Marcantoni, E.3
Palmieri, G.4
Chemo-, P.M.5
-
11
-
-
0033520236
-
Synthesis of N-substituted pyrrole and tetrahydroindole derivatives from alkenyl b-dicarbonyl compounds.
-
Ferraz, H. M. C.; Pereira, F. L. C.; Leite, F. S.; Nuns, M. R. S.; Payret-Arrua, M. E. Synthesis of N-substituted pyrrole and tetrahydroindole derivatives from alkenyl b-dicarbonyl compounds. Tetrahedron 1999, 55, 10915
-
(1999)
Tetrahedron
, vol.55
, pp. 10915
-
-
Ferraz, H.M.C.1
Pereira, F.L.C.2
Leite, F.S.3
Nuns, M.R.S.4
Payret-Arrua, M.E.5
-
12
-
-
10044293955
-
A facile synthesis of 2,3-disubstituted-6-arylpyridines from enaminones using montmorillonite K10 as solid acid support.
-
Reddy, G. J.; Latha, D.; Thirupathaiah, C.; Rao, K. S. A facile synthesis of 2,3-disubstituted-6-arylpyridines from enaminones using montmorillonite K10 as solid acid support. Tetrahedron Lett. 2005, 46, 301.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 301
-
-
Reddy, G.J.1
Latha, D.2
Thirupathaiah, C.3
Rao, K.S.4
-
13
-
-
0021041317
-
An improved procedure for the Blaise reaction: A short, practical route to the key intermediates of the saxitoxin synthesis
-
Hannick, S. M.; Kishi, Y. An improved procedure for the Blaise reaction: A short, practical route to the key intermediates of the saxitoxin synthesis. J. Org. Chem. 1983, 48, 3833
-
(1983)
J. Org. Chem.
, vol.48
, pp. 3833
-
-
Hannick, S.M.1
Kishi, Y.2
-
14
-
-
0000467813
-
1,2-Aryl and 1,2-hydride migration in transition metal complex catalyzed diazo decomposition: A novel approach to a-aryl-b-enamino esters
-
Jiang N.,Qu Z.,Wang J. 1,2-Aryl and 1,2-hydride migration in transition metal complex catalyzed diazo decomposition: A novel approach to a-aryl-b-enamino esters. Org. Lett. 2001, 3: 2989.
-
(2001)
Org. Lett.
, Issue.3
, pp. 2989
-
-
Jiang, N.1
Qu, Z.2
Wang, J.3
-
15
-
-
4143153949
-
The reaction of b-enaminoesters with organolithium reagents: A convenient method for the regioselective synthesis of enaminoketones.
-
Cimarelli, G.; Palmieri, G.; Volpini, E. The reaction of b-enaminoesters with organolithium reagents: A convenient method for the regioselective synthesis of enaminoketones. Tetrahedron Lett. 2004, 45, 6629
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 6629
-
-
Cimarelli, G.1
Palmieri, G.2
Volpini, E.3
-
16
-
-
0034529658
-
Imine acylation via benzotriazole derivatives: The preparation of enaminones.
-
Katritzky, A. R.; Fang, Y.; Donkor, A.; Xu, J. Imine acylation via benzotriazole derivatives: The preparation of enaminones. Synthesis 2000, 2029
-
(2000)
Synthesis
, vol.2029
-
-
Katritzky, A.R.1
Fang, Y.2
Donkor, A.3
Xu, J.4
-
17
-
-
0031794248
-
Synthesis and reactivity of new b-enamino acid derivatives: A simple and general approach to b-enamino esters and thioesters
-
Fustero, S.; de la Torre, M. G.; Jofre, V.; Carlon, R. P.; Navarro, A.; Fuentes, A. S.; Carrio, J. S. Synthesis and reactivity of new b-enamino acid derivatives: A simple and general approach to b-enamino esters and thioesters. J. Org. Chem. 1998, 63, 8825.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 8825
-
-
Fustero, S.1
De La Torre, M.G.2
Jofre, V.3
Carlon, R.P.4
Navarro, A.5
Fuentes, A.S.6
Carrio, J.S.7
-
18
-
-
37049127487
-
Enamine chemistry, XIV: Reaction of a,b-unsaturated acid chlorides with tertiary enamino ketones and esters
-
Hickmott, P. W.; Sheppard, G. Enamine chemistry, XIV: Reaction of a,b-unsaturated acid chlorides with tertiary enamino ketones and esters. J. Chem. Soc., Perkin Trans. 1 1972, 1038
-
(1972)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 1038
-
-
Hickmott, P.W.1
Sheppard, G.2
-
19
-
-
0034532847
-
New potential antimalarial agents: Synthesis and biological activities of original diaza-analogs of phenanthrene
-
1886
-
Yapi, A. D.; Mustofa, M.; Valentin, A.; Chavignon, O.; Teulade, J. C.; Mallie, M.; Chapat, J. P.; Blache, Y. New potential antimalarial agents: Synthesis and biological activities of original diaza-analogs of phenanthrene. Chem. Pharm. Bull. 2000, 48, 1886
-
(2000)
Chem. Pharm. Bull.
, vol.48
-
-
Yapi, A.D.1
Mustofa, M.2
Valentin, A.3
Chavignon, O.4
Teulade, J.C.5
Mallie, M.6
Chapat, J.P.7
Blache, Y.8
-
20
-
-
12444323717
-
The synthesis of oximes
-
Brown, R. J.; Carver, F. W. S.; Hollingsworth, B. L. The synthesis of oximes. J. Org. Chem. 1967, 32, 2624
-
(1967)
J. Org. Chem.
, vol.32
, pp. 2624
-
-
Brown, R.J.1
Carver, F.W.S.2
Hollingsworth, B.L.3
-
21
-
-
3142767629
-
Efficient synthetic method for b-enamino esters using ultrasound.
-
Brandt, C. A.; da Silva, A. C. M. P.; Pancote, C. G.; Brito, C. L.; da Silveira, M. A. B. Efficient synthetic method for b-enamino esters using ultrasound. Synthesis 2004, 1557
-
(2004)
Synthesis
, vol.1557
-
-
Brandt, C.A.1
Da Silva, A.C.M.P.2
Pancote, C.G.3
Brito, C.L.4
Da Silveira, M.A.B.5
-
22
-
-
0031827953
-
The use of K-10=ultrasound in the selective synthesis of unsymmetrical-enamino ketones.
-
Valduga, C. J.; Squizani, A.; Braibante, H. S.; Braibante, M. E. F. The use of K-10=ultrasound in the selective synthesis of unsymmetrical-enamino ketones. Synthesis 1998, 1019
-
(1998)
Synthesis
, vol.1019
-
-
Valduga, C.J.1
Squizani, A.2
Braibante, H.S.3
Braibante, M.E.F.4
-
23
-
-
1642369626
-
A new regio-and chemoselective approach to b-keto amides and b-enamino carboxamides via 1, 3,2-dioxaborinanes
-
Stefane, B.; Polanc, S. A new regio-and chemoselective approach to b-keto amides and b-enamino carboxamides via 1,3,2-dioxaborinanes. Synlett 2004, 698
-
(2004)
Synlett
, pp. 698
-
-
Stefane, B.1
Polanc, S.2
-
24
-
-
1642410348
-
A Convenient and Effective Method for Synthesizing B-amino-a, B-unsaturated Esters and Ketones
-
Gao, Y. H.; Zhang, Q. H.; Xu, J. X. A Convenient and effective method for synthesizing b-amino-a, b-unsaturated esters and ketones. Synth. Commun. 2004, 34, 909
-
(2004)
Synth. Commun.
, vol.34
, pp. 909
-
-
Gao, Y.H.1
Zhang, Q.H.2
Xu, J.X.3
-
25
-
-
1342344846
-
2O as a powerful catalyst for the conversion of b-ketoesters into b-enamino esters
-
Bartoli, G.; Bosco, M.; Locatelli, M.; Marcantoni, E.; Melchiorre, P.; Sambri, L. Zn(ClO4)2-6H2O as a powerful catalyst for the conversion of b-ketoesters into b-enamino esters. Synlett 2004, 239
-
(2004)
Synlett
, pp. 239
-
-
Bartoli, G.1
Bosco, M.2
Locatelli, M.3
Marcantoni, E.4
Melchiorre, P.5
Sambri, L.6
-
26
-
-
60849114194
-
2 O at ambient conditions: Ionic liquid and solvent-free media.
-
Khodaei, M. M.; Khosropour, A. R.; Kookhazadeh, M. Enamination of b-dicarbonyl compounds catalyzed by CeCl3-7H2O at ambient conditions: Ionic liquid and solvent-free media. Synlett 2004, 1980
-
(1980)
Synlett
, vol.2004
-
-
Khodaei, M.M.1
Khosropour, A.R.2
Kookhazadeh, M.3
-
27
-
-
0043154088
-
Gold catalysis in the reactions of 1,3-dicarbonyls with nucleophiles.
-
Arcadi, A.; Bianchi, G.; Di Giuseppe, S.; Marinelli, F. Gold catalysis in the reactions of 1,3-dicarbonyls with nucleophiles. Green Chem. 2003, 5, 64
-
(2003)
Green Chem.
, vol.5
, pp. 64
-
-
Arcadi, A.1
Bianchi, G.2
Di Giuseppe, S.3
Marinelli, F.4
-
28
-
-
1142288504
-
Natural clays as efficient catalysts for obtaining chiral b-enamino esters
-
Silva, F. C; Souza, M. C. B. V.; Ferreira, V. F.; Sabino, S. J.; Antunes, O. A. C. Natural clays as efficient catalysts for obtaining chiral b-enamino esters. Catal. Commun. 2004, 5, 151
-
(2004)
Catal. Commun.
, vol.5
, pp. 151
-
-
Silva, F.C.1
Souza, M.C.B.V.2
Ferreira, V.F.3
Sabino, S.J.4
Antunes, O.A.C.5
-
29
-
-
0842348272
-
3 as a reusable catalyst in aqueous media.
-
Khosropour, A. R.; Khodaei, M. M.; Kookhazadeh, M. A mild, efficient and environmentally friendly method for the regio-and chemoselective synthesis of enaminones using Bi(TFA)3 as a reusable catalyst in aqueous media. Tetrahedron Lett. 2004, 45, 1725
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 1725
-
-
Khosropour, A.R.1
Khodaei, M.M.2
Kookhazadeh, M.3
-
30
-
-
20044365621
-
3 immobilized on molten TBAB
-
Khodaei, M. M.; Khosropour, A. R.; Kookhazadeh, M. A novel enamination of b-dicarbonyl compounds catalyzed by Bi(TFA)3 immobilized on molten TBAB. Can. J. Chem. 2005, 83, 209
-
(2005)
Can. J. Chem.
, vol.83
, pp. 209
-
-
Khodaei, M.M.1
Khosropour, A.R.2
Kookhazadeh, M.3
-
31
-
-
29944445416
-
Thin-layer chromatography of enamino ketones.
-
Potesil, T. Thin-layer chromatography of enamino ketones. J. Chromatogr. 1984, 312, 387
-
(1984)
J. Chromatogr.
, vol.312
, pp. 387
-
-
Potesil, T.1
-
32
-
-
0033771259
-
An easy synthesis of enaminones in water as solvent.
-
Stefani, H. A.; Costa, I. M.; Silva, D. O. An easy synthesis of enaminones in water as solvent. Synthesis 2000, 1526
-
(2000)
Synthesis
, vol.1526
-
-
Stefani, H.A.1
Costa, I.M.2
Silva, D.O.3
-
33
-
-
32844458664
-
Highly efficient, mild and chemo-and stereoselective synthesis of enaminones and enamino esters using silica supported perchloric acid under solvent-free conditions
-
Das, B.; Venkateswarlu, K.; Majhi, A.; Reddy, M. R.; Reddy, K. N.; Rao, Y. K.; Ravikumar, K.; Sridhar, B. Highly efficient, mild and chemo-and stereoselective synthesis of enaminones and enamino esters using silica supported perchloric acid under solvent-free conditions. J. Mol. Catal. A: Chem. 2006, 246, 276
-
(2006)
J. Mol. Catal. A: Chem.
, vol.246
, pp. 276
-
-
Das, B.1
Venkateswarlu, K.2
Majhi, A.3
Reddy, M.R.4
Reddy, K.N.5
Rao, Y.K.6
Ravikumar, K.7
Sridhar, B.8
-
34
-
-
33747350324
-
3 catalyzed highly rapid and efficient synthesis of b-enamino compounds under solvent-free conditions
-
Yadav, J. S.; Kumar, V. N.; Rao, R. S.; Priyadarshini, A. D.; Rao, P. P.; Reddy, B. V. S.; Nagaiah, K. Sc(OTf)3 catalyzed highly rapid and efficient synthesis of b-enamino compounds under solvent-free conditions. J. Mol. Catal. A: Chem. 2006, 256, 234
-
(2006)
J. Mol. Catal. A: Chem.
, vol.256
, pp. 234
-
-
Yadav, J.S.1
Kumar, V.N.2
Rao, R.S.3
Priyadarshini, A.D.4
Rao, P.P.5
Reddy, B.V.S.6
Nagaiah, K.7
-
35
-
-
31544466241
-
A general and efficient method for the preparation of b-enamino ketones and esters catalyzed by indium tribromide
-
Zhang, Z. H.; Yin, L.; Wang, Y. M. A general and efficient method for the preparation of b-enamino ketones and esters catalyzed by indium tribromide. Adv. Synth. Catal. 2006, 348, 184
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 184
-
-
Zhang, Z.H.1
Yin, L.2
Wang, Y.M.3
-
36
-
-
33845410678
-
Chloride-mediated synthesis of b-enamino compounds under solvent-free conditions
-
Zhang, Z. H.; Hu, J. Y. Cobalt(II) chloride-mediated synthesis of b-enamino compounds under solvent-free conditions. J. Braz. Chem. Soc. 2006, 17, 1447
-
(2006)
J. Braz. Chem. Soc.
, vol.17
, pp. 1447
-
-
Zhang, Z.H.1
Cobalt II, Y.H.J.2
-
37
-
-
33947576867
-
Tertiary 3-aminoprope-nones and 3-aminopropenoates: Their preparation, with and without lewis acids, from secondary amines and 1,3-diketo compounds.
-
Vohra, R. K.; Renaud, J. L.; Bruneau, C. Tertiary 3-aminoprope-nones and 3-aminopropenoates: Their preparation, with and without lewis acids, from secondary amines and 1,3-diketo compounds. Synthesis 2007, 731, and references therein.
-
(2007)
Synthesis
, vol.731
-
-
Vohra, R.K.1
Renaud, J.L.2
Bruneau, C.3
-
38
-
-
0344240163
-
Synthesis and antioxidant activity of new tetraaryl pyrroles
-
Lehuedu, J.; Fauconneau, B.; Barrier, L.; Ourakow, M.; Piriou, A.; Vierfond, J. M. Synthesis and antioxidant activity of new tetraaryl pyrroles. Eur. J. Med. Chem. 1999, 34: 991
-
(1999)
Eur. J. Med. Chem
, vol.34
, pp. 991
-
-
Lehuedu, J.1
Fauconneau, B.2
Barrier, L.3
Ourakow, M.4
Piriou, A.5
Vierfond, J.M.6
-
39
-
-
0037027989
-
Antitumor imidazotetrazines 41: Conjugation of the antitumor agents mitozolomide and temozolomide to peptides and lexitropsins bearing DNA major and minor groove-binding structural motifs
-
Arrowsmith, J.; Jennings, S. A.; Clark, A. S.; Stevens, M. F. G. Antitumor imidazotetrazines, 41: Conjugation of the antitumor agents mitozolomide and temozolomide to peptides and lexitropsins bearing DNA major and minor groove-binding structural motifs. J. Med. Chem. 2002, 45, 5458
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5458
-
-
Arrowsmith, J.1
Jennings, S.A.2
Clark, A.S.3
Stevens, M.F.G.4
-
40
-
-
0033229862
-
Design, synthesis and binding properties of novel and selective dopamine D4 receptor ligands
-
Haubmann, C; Hubner, H.; Gmeiner, P. Piperidinyl-pyrroles: Design, synthesis and binding properties of novel and selective dopamine D4 receptor ligands. Bioorg. Med. Chem. Lett. 1999, 9, 3143.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 3143
-
-
Haubmann, C.1
Hubner, H.2
Piperidinyl-Pyrroles, G.P.3
-
41
-
-
85032569251
-
Stereochemical arrangement of atoms in molecules containing nitrogen
-
Hantzsch, A. Stereochemical arrangement of atoms in molecules containing nitrogen. Ber. Dtsch. Chem. Ges. 1890, 23, 1474
-
(1890)
Ber. Dtsch. Chem. Ges.
, vol.23
, pp. 1474
-
-
Hantzsch, A.1
-
42
-
-
37049087845
-
On the mechanism of pyrrole formation in the knorr pyrrole synthesis and by porphobilinogen synthase
-
Fabiano, E.; Golding, B. T. On the mechanism of pyrrole formation in the knorr pyrrole synthesis and by porphobilinogen synthase. J. Chem. Soc., Perkin Trans. 1 1991, 3371
-
(1991)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 3371
-
-
Fabiano, E.1
Golding, B.T.2
-
43
-
-
0035648701
-
Recent advances in the synthesis of pyrroles
-
Ferreira, V. F.; De Souza, M. C. B. V.; Cunha, A. C.; Pereira, L. O. R.; Ferreira, M. L. G. Recent advances in the synthesis of pyrroles. Org. Prep. Proced. Int. 2002, 33, 411
-
(2002)
Org. Prep. Proced. Int.
, vol.33
, pp. 411
-
-
Ferreira, V.F.1
De Souza, M.C.B.V.2
Cunha, A.C.3
Pereira, L.O.R.4
Ferreira, M.L.G.5
-
44
-
-
33845451797
-
A novel route to certain 2-pyrrolecarboxylic esters and nitriles
-
Kleinspehn, G. G. A novel route to certain 2-pyrrolecarboxylic esters and nitriles. J. Am. Chem. Soc. 1955, 77, 1546
-
(1955)
J. Am. Chem. Soc.
, vol.77
, pp. 1546
-
-
Kleinspehn, G.G.1
-
45
-
-
0000706504
-
C. a-Amino ketones from amino acids as precursors for the knorr pyrrole synthesis.
-
Hamby, J. M.; Hodges, J. C. a-Amino ketones from amino acids as precursors for the knorr pyrrole synthesis. Heterocycles 1993, 35, 843
-
(1993)
Heterocycles
, vol.35
, pp. 843
-
-
Hamby, J.M.1
Hodges, J.2
-
46
-
-
0033591154
-
Versatility of Weinreb amides in the knorr pyrrole synthesis.
-
Alberola, A.; Ortega, A. G.; Sadaba, M. L.; Sanudo, C. Versatility of Weinreb amides in the knorr pyrrole synthesis. Tetrahedron 1999, 55, 6555
-
(1999)
Tetrahedron
, vol.55
, pp. 6555
-
-
Alberola, A.1
Ortega, A.G.2
Sadaba, M.L.3
Sanudo, C.4
-
48
-
-
3242766765
-
4 as novel and reusable catalytic system for the synthesis of furan, pyrrole, and thiophene derivatives.
-
Yadav, J. S.; Reddy, B. V. S.; Eeshwaraiah, B.; Gupta, M. K. Bi(OTf)3=[bmim]BF4 as novel and reusable catalytic system for the synthesis of furan, pyrrole, and thiophene derivatives. Tetrahedron Lett. 2004, 45, 5873
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 5873
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Eeshwaraiah, B.3
Gupta, M.K.4
-
49
-
-
0035909591
-
A novel one-pot pyrrole synthesis via a coupling-isomerization-Stetter= Paal-Knorr sequence
-
Braun, R. U.; Zeitler, K.; Mueller, T. J. J. A novel one-pot pyrrole synthesis via a coupling-isomerization-Stetter=Paal-Knorr sequence. Org. Lett. 2001, 3, 3297
-
(2001)
Org. Lett.
, vol.3
, pp. 3297
-
-
Braun, R.U.1
Zeitler, K.2
Mueller, T.J.J.3
-
50
-
-
0037433806
-
Layered zirconium phosphate and phosphonate as heterogeneous catalyst in the preparation of pyrroles.
-
Curini, M.; Montanari, F.; Rosati, O.; Lioy, E.; Margarita, R. Layered zirconium phosphate and phosphonate as heterogeneous catalyst in the preparation of pyrroles. Tetrahedron Lett. 2003, 44, 3923
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3923
-
-
Curini, M.1
Montanari, F.2
Rosati, O.3
Lioy, E.4
Margarita, R.5
-
51
-
-
0347991827
-
Simple synthesis of substituted pyrroles
-
Banik, B. K.; Samajdar, S.; Banik, I. Simple synthesis of substituted pyrroles. J. Org. Chem. 2004, 69, 213
-
(2004)
J. Org. Chem.
, vol.69
, pp. 213
-
-
Banik, B.K.1
Samajdar, S.2
Banik, I.3
-
52
-
-
11144250168
-
Heterocycle synthesis: Pyrrole syntheses by multicomponent coupling reactions
-
Balme, G. Heterocycle synthesis: Pyrrole syntheses by multicomponent coupling reactions. Angew. Chem., Int. Ed. 2004, 43, 6238
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 6238
-
-
Balme, G.1
-
53
-
-
3242695438
-
Catalytic multicomponent synthesis of highly substituted pyrroles utilizing a one-pot Sila-Stetter=Paal-Knorr strategy
-
Bharadwaj, A. R.; Scheidt, K. A. Catalytic multicomponent synthesis of highly substituted pyrroles utilizing a one-pot Sila-Stetter=Paal-Knorr strategy. Org. Lett. 2004, 6, 2465
-
(2004)
Org. Lett.
, vol.6
, pp. 2465
-
-
Bharadwaj, A.R.1
Scheidt, K.A.2
-
54
-
-
0034093338
-
2, 5-Dialkylfurans and nitro alkanes as source of 2, 3,5-trialkylpyr- roles
-
Ballini, R.; Barboni, L.; Bosica, G.; Petrini, M. 2,5-Dialkylfurans and nitro alkanes as source of 2,3,5-trialkylpyr-roles. Synlett 2000, 391
-
(2000)
Synlett
, pp. 391
-
-
Ballini, R.1
Barboni, L.2
Bosica, G.3
Petrini, M.4
-
55
-
-
0037263786
-
Solid-phase synthesis of heterocycles from 1,4-diketone synthons.
-
Raghavan, S.; Anuradha, K. Solid-phase synthesis of heterocycles from 1,4-diketone synthons. Synlett 2003, 711
-
(2003)
Synlett
, vol.711
-
-
Raghavan, S.1
Anuradha, K.2
-
56
-
-
0037240917
-
A practical variation on the Paal-Knorr pyrrole synthesis.
-
Quiclet-Sire, B.; Quintero, L.; Sanchez-Jimenez, G.; Zard, Z. A practical variation on the Paal-Knorr pyrrole synthesis. Synlett 2003, 75
-
(2003)
Synlett
, vol.75
-
-
Quiclet-Sire, B.1
Quintero, L.2
Sanchez-Jimenez, G.3
Zard, Z.4
-
57
-
-
1842788687
-
Pyrrole synthesis in ionic liquids by Paal-Knorr condensation under mild conditions
-
Wang, B.; Gu, Y. L.; Luo, C.;Yang, T.; Yang, L. M.; Suo, J. S. Pyrrole synthesis in ionic liquids by Paal-Knorr condensation under mild conditions. Tetrahedron Lett. 2004, 45, 3417
-
(2004)
Tetrahedron Lett.
, Issue.45
, pp. 3417
-
-
Wang, B.1
Gu, Y.L.2
Luo, C.3
Yang, T.4
Yang, L.M.5
Suo, J.S.6
-
58
-
-
17044437759
-
3-Mon-tmorillonite as effective, recyclable catalyst for Paal-Knorr pyrrole synthesis under mild conditions
-
Wang, B.; Kang, Y. R.; Yang, T.; Yang, L. M. Fe3-Mon-tmorillonite as effective, recyclable catalyst for Paal-Knorr pyrrole synthesis under mild conditions. Synth. Commun. 2005, 35, 1051.
-
(2005)
Synth. Commun.
, vol.35
, pp. 1051
-
-
Wang, B.1
Kang, Y.R.2
Yang, T.3
Yang, L.M.4
-
59
-
-
0001893443
-
Rapid generation of amines by microwave irradiation of ureas dispersed on clay.
-
Ruault, P.; Pilard, J. F.; Touaux, B.; Boullet, F. T.; Hamelin, J. Rapid generation of amines by microwave irradiation of ureas dispersed on clay. Synlett 1994, 935
-
(1994)
Synlett
, vol.935
-
-
Ruault, P.1
Pilard, J.F.2
Touaux, B.3
Boullet, F.T.4
Hamelin, J.5
-
60
-
-
0033553540
-
Microwave assisted synthesis of pyrroles.
-
Danks, T. N. Microwave assisted synthesis of pyrroles. Tetrahedron Lett. 1999, 40, 3957
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3957
-
-
Danks, T.N.1
-
61
-
-
30044440260
-
Microwave-assisted Paal-Knorr reaction-Three-step regiocon-trolled synthesis of polysubstituted furans, pyrroles, and thiophenes
-
Minetto, G.; Raveglia, L. F.; Sega, A.; Taddei, M. Microwave-assisted Paal-Knorr reaction-Three-step regiocon-trolled synthesis of polysubstituted furans, pyrroles, and thiophenes. Eur. J. Org. Chem. 2005, 5277
-
(2005)
Eur. J. Org. Chem.
, vol.5277
-
-
Minetto, G.1
Raveglia, L.F.2
Sega, A.3
Taddei, M.4
-
62
-
-
1342285524
-
Microwave-assisted Paal-Knorr reaction: A rapid approach to substituted pyrroles and furans
-
Minetto, G.; Raveglia, L. F.; Taddei, M. Microwave-assisted Paal-Knorr reaction: A rapid approach to substituted pyrroles and furans. Org. Lett. 2004, 3, 389.
-
(2004)
Org. Lett.
, vol.3
, pp. 389
-
-
Minetto, G.1
Raveglia, L.F.2
Taddei, M.3
-
63
-
-
33846591918
-
Efficient one-pot synthesis of fluorinated benzimidazolines, benzothiazolines, benzoxazolines, and dihydrobenzoxazi-nones using gallium(III) triflate as a catalyst
-
Prakash, G. K. S.; Mathew, T.; Panja, C.; Vaghoo, H.; Venkataraman, K.; Olah, G. A. Efficient one-pot synthesis of fluorinated benzimidazolines, benzothiazolines, benzoxazolines, and dihydrobenzoxazi-nones using gallium(III) triflate as a catalyst. Org. Lett. 2007, 9, 179
-
(2007)
Org. Lett.
, vol.9
, pp. 179
-
-
Prakash, G.K.S.1
Mathew, T.2
Panja, C.3
Vaghoo, H.4
Venkataraman, K.5
Olah, G.A.6
-
64
-
-
23044492621
-
Highly regioselective rearrangement of 2-substituted vinylepoxides catalyzed by gallium(III) triflate
-
Deng, X. M.; Sun, X. L.; Tang, Y. Highly regioselective rearrangement of 2-substituted vinylepoxides catalyzed by gallium(III) triflate. J. Org. Chem. 2005, 70, 6537
-
(2005)
J. Org. Chem.
, vol.70
, pp. 6537
-
-
Deng, X.M.1
Sun, X.L.2
Tang, Y.3
-
65
-
-
29044450579
-
An annulation toward fused bicy-clolactones
-
Nguyen, R. V.; Li, C. J. An annulation toward fused bicy-clolactones. J. Am. Chem. Soc. 2005, 127, 17184.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17184
-
-
Nguyen, R.V.1
Li, C.J.2
-
66
-
-
23244444900
-
One-pot synthesis of dihy-dropyrimidiones catalyzed by strontium(II) triflate under solvent-free conditions.
-
Su, W. K.; Li, J. J.; Zheng, Z. G.; Shen, Y. C. One-pot synthesis of dihy-dropyrimidiones catalyzed by strontium(II) triflate under solvent-free conditions. Tetrahedron Lett. 2005, 46, 6037
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 6037
-
-
Su, W.K.1
Li, J.J.2
Zheng, Z.G.3
Shen, Y.C.4
-
67
-
-
33745671357
-
A facile synthesis of 1-substituted-1H-1 2, 3,4-tetrazoles catalyzed by ytterbium triflate hydrate
-
Su, W. K.; Hong, Z.; Shan, W. G.; Zhang, X. X. A facile synthesis of 1-substituted-1H-1,2,3,4-tetrazoles catalyzed by ytterbium triflate hydrate. Eur. J. Org. Chem. 2006, 2723
-
(2006)
Eur. J. Org. Chem.
, pp. 2723
-
-
Su, W.K.1
Hong, Z.2
Shan, W.G.3
Zhang, X.X.4
-
68
-
-
33947235817
-
Ytterbium(III) triflate catalyzed [3 + 2] cycload-dition of N-aryl imines and epoxides: A novel and solvent-free synthesis of substituted 1,3-oxazolidines
-
Yu C. M.,Dai X. P.,Su W. K. Ytterbium(III) triflate catalyzed [3 + 2] cycload-dition of N-aryl imines and epoxides: A novel and solvent-free synthesis of substituted 1,3-oxazolidines. Synlett, 2007: 646.
-
(2007)
Synlett
, vol.646
-
-
Yu, C.M.1
Dai, X.P.2
Su, W.K.3
-
69
-
-
33745195009
-
3 under solvent-free conditions.
-
Chen, J. X.; Wu, H. Y.; Zheng, Z. G.; Jin, C.; Zhang, X. X.; Su, W. K. An approach to the Paal-Knorr pyrroles synthesis catalyzed by Sc(OTf)3 under solvent-free conditions. Tetrahedron Lett. 2006, 47, 5383
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 5383
-
-
Chen, J.X.1
Wu, H.Y.2
Zheng, Z.G.3
Jin, C.4
Zhang, X.X.5
Su, W.K.6
-
70
-
-
34250204873
-
A general and efficient method for the selective synthesis of b-hydroxy sul-fides and b-hydroxy sulfoxides catalyzed by gallium(III) triflate
-
Su, W. K.; Chen, J. X.; Wu, H. Y.; Jin, C. A general and efficient method for the selective synthesis of b-hydroxy sul-fides and b-hydroxy sulfoxides catalyzed by gallium(III) triflate. J. Org. Chem. 2007, 72, 4524
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4524
-
-
Su, W.K.1
Chen, J.X.2
Wu, H.Y.3
Jin, C.4
-
71
-
-
33947589434
-
First catalytic and green synthesis of Aryl-(Z)-vinyl chlorides and its plausible addition-elimination mechanism
-
Su, W. K.; Jin, C. First catalytic and green synthesis of Aryl-(Z)-vinyl chlorides and its plausible addition-elimination mechanism. Org. Lett. 2007, 9, 993
-
(2007)
Org. Lett.
, vol.9
, pp. 993
-
-
Su, W.K.1
Jin, C.2
-
72
-
-
8644240882
-
One-step reaction of Friedel-Crafts acylation and demethylation of aryl-methyl ethers catalyzed by ytter-bium(III) triflate
-
Su, W. K.; Jin, C. One-step reaction of Friedel-Crafts acylation and demethylation of aryl-methyl ethers catalyzed by ytter-bium(III) triflate. Synth. Commun. 2004, 34, 4199
-
(2004)
Synth. Commun.
, vol.34
, pp. 4199
-
-
Su, W.K.1
Jin, C.2
-
73
-
-
10644237031
-
Ytterbium triflate-catalyzed Friedel-Crafts reaction: Facile synthesis of diaryl ketones
-
Ytterbium triflate-catalyzed Friedel-Crafts reaction: Facile synthesis of diaryl ketones. Synth. Commun. 2004, 34, 4249
-
(2004)
Synth. Commun.
, vol.34
, pp. 4249
-
-
-
74
-
-
20844459502
-
Novel process for synthesis of 1 2,4-triazoles: Ytterbium triflate-catalyzed cyclization of hydrazonyl chlorides with nitriles
-
Su, W. K.; Yang, D. W.; Li, J. J. Novel process for synthesis of 1,2,4-triazoles: Ytterbium triflate-catalyzed cyclization of hydrazonyl chlorides with nitriles. Synth. Commun. 2005, 35, 1435
-
(2005)
Synth. Commun.
, Issue.35
, pp. 1435
-
-
Su, W.K.1
Yang, D.W.2
Li, J.J.3
-
75
-
-
33645456496
-
Highly regio-selective ring opening of epoxides with thiophenols in ionic liquids without the use of any catalyst.
-
Chen, J. X.; Wu, H. Y.; Jin, C.; Zhang, X. X.; Xie, Y. Y.; Su, W. K. Highly regio-selective ring opening of epoxides with thiophenols in ionic liquids without the use of any catalyst. Green Chem. 2006, 8, 330
-
(2006)
Green Chem.
, vol.8
, pp. 330
-
-
Chen, J.X.1
Wu, H.Y.2
Jin, C.3
Zhang, X.X.4
Xie, Y.Y.5
Su, W.K.6
-
76
-
-
34548215079
-
Eco-friendly synthesis of 2,3-dihydroquinazolin-4(1H)-ones in ionic liquids or ionic liquid-water without additional catalyst.
-
Chen, J. X.; Su, W. K.; Wu, H. Y.; Liu, M. C.; Jin, C. Eco-friendly synthesis of 2,3-dihydroquinazolin-4(1H)-ones in ionic liquids or ionic liquid-water without additional catalyst. Green Chem. 2007, 9, 972
-
(2007)
Green Chem.
, vol.9
, pp. 972
-
-
Chen, J.X.1
Su, W.K.2
Wu, H.Y.3
Liu, M.C.4
Jin, C.5
-
77
-
-
35548982108
-
Solvent-free synthesis of b-hydroxy esters and b-amino esters by indium-mediated reformatsky reaction.
-
Chen, X. A.; Zhang, C. F.; Wu, H. Y.; Yu, X. C.; Su, W. K.; Cheng, J. Solvent-free synthesis of b-hydroxy esters and b-amino esters by indium-mediated reformatsky reaction. Synthesis 2007, 3233.
-
(2007)
Synthesis
, vol.3233
-
-
Chen, X.A.1
Zhang, C.F.2
Wu, H.Y.3
Yu, X.C.4
Su, W.K.5
Cheng, J.6
-
78
-
-
0031486613
-
17O NMR spec-troscopic studies of acyclic and cyclic N-aryl enaminones: Substituent effects and intramolecular hydrogen bonding
-
Zhou, J. C. NMR of enaminones, part 3: 1H, 13C, and 17O NMR spec-troscopic studies of acyclic and cyclic N-aryl enaminones: Substituent effects and intramolecular hydrogen bonding. Magn. Reson. Chem. 1997, 35, 311.
-
(1997)
Magn. Reson. Chem.
, Issue.35
, pp. 311
-
-
Zhou, J.C.1
-
79
-
-
33947445004
-
The reactions of unsaturated ketones and derivatives with amino compounds: Amino ketones
-
Coromwell, N. H. The reactions of unsaturated ketones and derivatives with amino compounds: Amino ketones. Chem. Rev. 1946, 38, 83.
-
(1946)
Chem. Rev.
, vol.38
, pp. 83
-
-
Coromwell, N.H.1
-
80
-
-
22544470276
-
Synthesis NMR, and x-ray characterisation of 6-substituted 4-amino-5-aryldiazenyl-1-arylpyridazinium salts.
-
Simunek, P.; Peskova, M.; Bertolasi, V.; Machacek, V.; Lycka, A. Synthesis, NMR, and x-ray characterisation of 6-substituted 4-amino-5- aryldiazenyl-1-arylpyridazinium salts. Tetrahedron 2005, 61, 8130.
-
(2005)
Tetrahedron
, vol.61
, pp. 8130
-
-
Simunek, P.1
Peskova, M.2
Bertolasi, V.3
MacHacek, V.4
Lycka, A.5
-
81
-
-
37049122265
-
Reaction of 1, 2-and 1,3-dicarbonyl compounds with 1,3-diamines: Some new 1,4-diazepines
-
McDougall, R. H.; Malik, S. H. Reaction of 1,2-and 1,3-dicarbonyl compounds with 1,3-diamines: Some new 1,4-diazepines. J. Chem. Soc. 1969, 2044.
-
(1969)
J. Chem. Soc.
, pp. 2044
-
-
McDougall, R.H.1
Malik, S.H.2
-
82
-
-
33947465481
-
Inner complex chelates, II: Analogs and polar substituted analogs of bis(acetylacetone) ethylenediimine and its metal chelates
-
Hovey, R. J.; O'Connell, J. J.; Martell, A. E. Inner complex chelates, II: Analogs and polar substituted analogs of bis(acetylacetone) ethylenediimine and its metal chelates. J. Am. Chem. Soc. 1959, 81, 3189.
-
(1959)
J. Am. Chem. Soc.
, vol.81
, pp. 3189
-
-
Hovey, R.J.1
O'Connell, J.J.2
Martell, A.E.3
-
83
-
-
0007674578
-
2,5-dimethylpyrrole derivatives
-
Bishop, W. S. 2,5-dimethylpyrrole derivatives. J. Am. Chem. Soc. 1945, 67, 2261.
-
(1945)
J. Am. Chem. Soc.
, Issue.67
, pp. 2261
-
-
Bishop, W.S.1
-
84
-
-
0000619013
-
Trifluoroacetylation at the 3-position of 1-(2-aminophenyl)-2,5- dimethylpyrrole in trifluoroacetic acid: Possible remote control of an amino group in electrophilic substitution
-
Imuro, K.; Hanafusa, T. Trifluoroacetylation at the 3-position of 1-(2-aminophenyl)-2,5-dimethylpyrrole in trifluoroacetic acid: Possible remote control of an amino group in electrophilic substitution. Bull. Chem. Soc. Jpn. 1976, 49, 1363.
-
(1976)
Bull. Chem. Soc. Jpn.
, vol.49
, pp. 1363
-
-
Imuro, K.1
Hanafusa, T.2
-
85
-
-
85078397894
-
Pyrrole and pyrazole ring closure in heterogeneous media.
-
Texier-Boullet, F.; Klein, B.; Hamelin, J. Pyrrole and pyrazole ring closure in heterogeneous media. Synthesis 1986, 409.
-
(1986)
Synthesis
, vol.409
-
-
Texier-Boullet, F.1
Klein, B.2
Hamelin, J.3
|