-
1
-
-
84981756782
-
Ueber eine neue bildungsweise von diphenylaminderivaten
-
Ullmann, F. Ueber eine neue bildungsweise von diphenylaminderivaten Chem. Ber. 1903, 36, 2382-2384
-
(1903)
Chem. Ber.
, vol.36
, pp. 2382-2384
-
-
Ullmann, F.1
-
2
-
-
84973392158
-
Ueber synthesen in der biphenylreihe
-
Ullmann, F.; Bielecki, J. Ueber synthesen in der biphenylreihe Chem. Ber. 1901, 34, 2174-2185
-
(1901)
Chem. Ber.
, vol.34
, pp. 2174-2185
-
-
Ullmann, F.1
Bielecki, J.2
-
3
-
-
0003677260
-
Ueber die phenylirung von phenolen
-
Ullmann, F.; Sponagel, P. Ueber die phenylirung von phenolen Chem. Ber. 1905, 36, 2211-2212
-
(1905)
Chem. Ber.
, vol.36
, pp. 2211-2212
-
-
Ullmann, F.1
Sponagel, P.2
-
4
-
-
84971062653
-
Concerning phenylization in the presence of copper as a catalytic agent
-
Goldberg, I. Concerning phenylization in the presence of copper as a catalytic agent Chem. Ber. 1906, 39, 1691-1692
-
(1906)
Chem. Ber.
, vol.39
, pp. 1691-1692
-
-
Goldberg, I.1
-
5
-
-
2742585020
-
Syntheses of cyclic bisbibenzyl systems
-
Eicher, T.; Fey, S.; Puhl, W.; Büchel, E.; Speicher, A. Syntheses of cyclic bisbibenzyl systems Eur. J. Org. Chem. 1998, 1998 (5) 877-888
-
(1998)
Eur. J. Org. Chem.
, vol.1998
, Issue.5
, pp. 877-888
-
-
Eicher, T.1
Fey, S.2
Puhl, W.3
Büchel, E.4
Speicher, A.5
-
6
-
-
0032538575
-
Total syntheses of vancomycin and eremomycin aglycons
-
Evans, D. A.; Wood, M. R.; Trotter, B. W.; Richardson, T. I.; Barrow, J. C.; Katz, J. L. Total syntheses of vancomycin and eremomycin aglycons Angew. Chem., Int. Ed. 1998, 37 (19) 2700-2704
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, Issue.19
, pp. 2700-2704
-
-
Evans, D.A.1
Wood, M.R.2
Trotter, B.W.3
Richardson, T.I.4
Barrow, J.C.5
Katz, J.L.6
-
7
-
-
0041528352
-
A novel polycarbonate for high temperature electro-optics via azo bisphenol amines accessed by Ullmann coupling
-
Suresh, S.; Gulotty, R. J., Jr.; Bales, S. E.; Inbasekaran, M. N.; Chartier, M. A.; Cummins, C.; Smith, D. W., Jr. A novel polycarbonate for high temperature electro-optics via azo bisphenol amines accessed by Ullmann coupling Polymer 2003, 44 (18) 5111-5117
-
(2003)
Polymer
, vol.44
, Issue.18
, pp. 5111-5117
-
-
Suresh, S.1
Gulotty Jr., R.J.2
Bales, S.E.3
Inbasekaran, M.N.4
Chartier, M.A.5
Cummins, C.6
Smith Jr., D.W.7
-
8
-
-
0030780953
-
Palladium-catalyzed formation of diaryl ethers from aryl bromides. Electron poor phosphines enhance reaction yields
-
Mann, G.; Hartwig, J. F. Palladium-catalyzed formation of diaryl ethers from aryl bromides. Electron poor phosphines enhance reaction yields Tetrahedron Lett. 1997, 38 (46) 8005-8008
-
(1997)
Tetrahedron Lett.
, vol.38
, Issue.46
, pp. 8005-8008
-
-
Mann, G.1
Hartwig, J.F.2
-
9
-
-
0033531744
-
Palladium-catalyzed C-O coupling involving unactivated aryl halides. Sterically induced reductive elimination to form the C-O bond in diaryl ethers
-
Mann, G.; Incarvito, C.; Rheingold, A. L.; Hartwig, J. F. Palladium-catalyzed C-O coupling involving unactivated aryl halides. Sterically induced reductive elimination to form the C-O bond in diaryl ethers J. Am. Chem. Soc. 1999, 121 (13) 3224-3225
-
(1999)
J. Am. Chem. Soc.
, vol.121
, Issue.13
, pp. 3224-3225
-
-
Mann, G.1
Incarvito, C.2
Rheingold, A.L.3
Hartwig, J.F.4
-
10
-
-
0033549049
-
Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers
-
Aranyos, A.; Old, D. W.; Kiyomori, A.; Wolfe, J. P.; Sadighi, J. P.; Buchwald, S. L. Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers J. Am. Chem. Soc. 1999, 121 (18) 4369-4378
-
(1999)
J. Am. Chem. Soc.
, vol.121
, Issue.18
, pp. 4369-4378
-
-
Aranyos, A.1
Old, D.W.2
Kiyomori, A.3
Wolfe, J.P.4
Sadighi, J.P.5
Buchwald, S.L.6
-
11
-
-
0345708168
-
Modern synthetic methods for copper-mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S Bond Formation
-
Ley, S. V.; Thomas, A. W. Modern synthetic methods for copper-mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S Bond Formation Angew. Chem., Int. Ed. 2003, 42 (44) 5400-5449
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, Issue.44
, pp. 5400-5449
-
-
Ley, S.V.1
Thomas, A.W.2
-
12
-
-
70349786460
-
Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions
-
Monnier, F.; Taillefer, M. Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions Angew. Chem., Int. Ed. 2009, 48 (38) 6954-6971
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, Issue.38
, pp. 6954-6971
-
-
Monnier, F.1
Taillefer, M.2
-
13
-
-
0035842155
-
Expanding the diversity of purine libraries
-
Ding, S.; Gray, N. S.; Ding, Q.; Schultz, P. G. Expanding the diversity of purine libraries Tetrahedron Lett. 2001, 42, 8751-8755
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8751-8755
-
-
Ding, S.1
Gray, N.S.2
Ding, Q.3
Schultz, P.G.4
-
14
-
-
0037047555
-
Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond-forming cross-couplings
-
Kataoka, N.; Shelby, Q.; Stambuli, J. P.; Hartwig, J. F. Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond-forming cross-couplings J. Org. Chem. 2002, 67 (16) 5553-5566
-
(2002)
J. Org. Chem.
, vol.67
, Issue.16
, pp. 5553-5566
-
-
Kataoka, N.1
Shelby, Q.2
Stambuli, J.P.3
Hartwig, J.F.4
-
15
-
-
0037007703
-
Ullmann diaryl ether synthesis: Rate acceleration by 2,2,6,6- tetramethylheptane-3,5-dione
-
Buck, E.; Song, Z. J.; Tschaen, D.; Dormer, P. G.; Volante, R. P.; Reider, P. J. Ullmann diaryl ether synthesis: Rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione Org. Lett. 2002, 4 (9) 1623-1626
-
(2002)
Org. Lett.
, vol.4
, Issue.9
, pp. 1623-1626
-
-
Buck, E.1
Song, Z.J.2
Tschaen, D.3
Dormer, P.G.4
Volante, R.P.5
Reider, P.J.6
-
16
-
-
0032492942
-
New N- and O-arylations with phenylboronic acids and cupric acetate
-
Chan, D. M. T.; Monaco, K. L.; Wang, R.-P.; Winters, M. P. New N- and O-arylations with phenylboronic acids and cupric acetate Tetrahedron Lett. 1998, 39 (19) 2933-2936
-
(1998)
Tetrahedron Lett.
, vol.39
, Issue.19
, pp. 2933-2936
-
-
Chan, D.M.T.1
Monaco, K.L.2
Wang, R.-P.3
Winters, M.P.4
-
17
-
-
1642528362
-
A general and mild Ullmann-type synthesis of diaryl ethers
-
Cristau, H. J.; Cellier, P. P.; Hamada, S.; Spindler, J. F.; Taillefer, M. A general and mild Ullmann-type synthesis of diaryl ethers Org. Lett. 2004, 6, 913-916
-
(2004)
Org. Lett.
, vol.6
, pp. 913-916
-
-
Cristau, H.J.1
Cellier, P.P.2
Hamada, S.3
Spindler, J.F.4
Taillefer, M.5
-
18
-
-
0032492980
-
Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine
-
Evans, D. A.; Katz, J. L.; West, T. R. Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine Tetrahedron Lett. 1998, 39 (19) 2937-2940
-
(1998)
Tetrahedron Lett.
, vol.39
, Issue.19
, pp. 2937-2940
-
-
Evans, D.A.1
Katz, J.L.2
West, T.R.3
-
19
-
-
0033593282
-
Ligand-accelerated catalysis of the Ullmann condensation: Application to hole conducting triarylamines
-
Goodbrand, H. B.; Hu, N. X. J. Ligand-accelerated catalysis of the Ullmann condensation: Application to hole conducting triarylamines J. Org. Chem. 1999, 64 (2) 670-674
-
(1999)
J. Org. Chem.
, vol.64
, Issue.2
, pp. 670-674
-
-
Goodbrand, H.B.1
Hu, N.X.J.2
-
20
-
-
0001572402
-
Formation of aryl-nitrogen, aryl-oxygen, and aryl-carbon bonds using well defined copper (i)-based catalyst
-
Gujadhur, R. K.; Bates, C. G.; Venkataraman, D. Formation of aryl-nitrogen, aryl-oxygen, and aryl-carbon bonds using well defined copper (i)-based catalyst Org. Lett. 2001, 3, 4315-4317
-
(2001)
Org. Lett.
, vol.3
, pp. 4315-4317
-
-
Gujadhur, R.K.1
Bates, C.G.2
Venkataraman, D.3
-
21
-
-
0032493017
-
New aryl/heteroaryl C···N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
-
Lam, P. Y. S.; Clark, C. G.; Saubern, S.; Adams, J.; Winters, M. P.; Chan, D. M. T.; Combs, A. New aryl/heteroaryl C···N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation Tetrahedron Lett. 1998, 39, 2941-2944
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2941-2944
-
-
Lam, P.Y.S.1
Clark, C.G.2
Saubern, S.3
Adams, J.4
Winters, M.P.5
Chan, D.M.T.6
Combs, A.7
-
22
-
-
0042347800
-
Copper-catalyzed amination of aromatic halides with 2- N, N -dimethylaminoethanol as solvent
-
Lu, Z.; Twieg, R. J.; Huang, S. D. Copper-catalyzed amination of aromatic halides with 2- N, N -dimethylaminoethanol as solvent Tetrahedron Lett. 2003, 44, 6289-6292
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6289-6292
-
-
Lu, Z.1
Twieg, R.J.2
Huang, S.D.3
-
23
-
-
0242543883
-
N, N -Dimethyl glycine-promoted Ullmann coupling reaction of phenols and aryl halides
-
Ma, D.; Cai, Q. N, N -Dimethyl glycine-promoted Ullmann coupling reaction of phenols and aryl halides Org. Lett. 2003, 5, 3799-3802
-
(2003)
Org. Lett.
, vol.5
, pp. 3799-3802
-
-
Ma, D.1
Cai, Q.2
-
24
-
-
0035833707
-
CuI-catalyzed coupling reaction of β-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857
-
Ma, D.; Xia, C. CuI-catalyzed coupling reaction of β-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857 Org. Lett. 2001, 3, 2583-2586
-
(2001)
Org. Lett.
, vol.3
, pp. 2583-2586
-
-
Ma, D.1
Xia, C.2
-
25
-
-
0030700314
-
A general copper-catalyzed synthesis of diaryl ethers
-
Marcoux, J. F.; Doye, S.; Buchwald, S. L. J. A general copper-catalyzed synthesis of diaryl ethers J. Am. Chem. Soc. 1997, 7863 (12) 10539-10540
-
(1997)
J. Am. Chem. Soc.
, vol.7863
, Issue.12
, pp. 10539-10540
-
-
Marcoux, J.F.1
Doye, S.2
Buchwald, S.L.J.3
-
26
-
-
0002888890
-
Phosphazene P4-But base for the Ullmann biaryl ether synthesis
-
Palomo, C.; Oiarbide, M.; Lopez, R.; Gomez-Bengoa, E. Phosphazene P4-But base for the Ullmann biaryl ether synthesis Chem. Commun. 1998, 19, 2091-2092
-
(1998)
Chem. Commun.
, vol.19
, pp. 2091-2092
-
-
Palomo, C.1
Oiarbide, M.2
Lopez, R.3
Gomez-Bengoa, E.4
-
27
-
-
77952894215
-
Cu-based nanoalloys in the base-free Ullmann heterocyle-aryl ether synthesis
-
Engels, V.; Benaskar, F.; Patil, N.; Rebrov, E. V.; Hessel, V.; Hulshof, L. A.; Jefferson, D. A.; Vekemans, J. A. J. M.; Karwal, S.; Schouten, J. C.; Wheatley, A. E. H. Cu-based nanoalloys in the base-free Ullmann heterocyle-aryl ether synthesis Org. Process Res. Dev. 2010, 14 (3) 644-649
-
(2010)
Org. Process Res. Dev.
, vol.14
, Issue.3
, pp. 644-649
-
-
Engels, V.1
Benaskar, F.2
Patil, N.3
Rebrov, E.V.4
Hessel, V.5
Hulshof, L.A.6
Jefferson, D.A.7
Vekemans, J.A.J.M.8
Karwal, S.9
Schouten, J.C.10
Wheatley, A.E.H.11
-
28
-
-
47749142816
-
Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions: Copper makes a difference
-
Monnier, F.; Taillefer, M. Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions: Copper makes a difference Angew. Chem., Int. Ed. 2008, 47 (17) 3096-3099
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, Issue.17
, pp. 3096-3099
-
-
Monnier, F.1
Taillefer, M.2
-
29
-
-
24944493399
-
Kinetics and mechanism of the reaction of substituted benzyl chlorides with copper in dimethylformamide
-
Egorov, A. M.; Matyukhova, S. A.; Anisimov, A. V. Kinetics and mechanism of the reaction of substituted benzyl chlorides with copper in dimethylformamide J. Phys. Org. Chem. 2005, 18 (10) 1023-1031
-
(2005)
J. Phys. Org. Chem.
, vol.18
, Issue.10
, pp. 1023-1031
-
-
Egorov, A.M.1
Matyukhova, S.A.2
Anisimov, A.V.3
-
30
-
-
77949377447
-
Copper(I) phenoxide complexes in the etherification of aryl halides
-
Tye, J. W.; Weng, Z.; Giri, R.; Hartwig, J. F. Copper(I) phenoxide complexes in the etherification of aryl halides Angew. Chem., Int. Ed. 2010, 49 (12) 2185-2189
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, Issue.12
, pp. 2185-2189
-
-
Tye, J.W.1
Weng, Z.2
Giri, R.3
Hartwig, J.F.4
-
31
-
-
0020829220
-
A spectroscopic investigation of the adsorption of phenol on Cu(110)
-
Richardson, N. V.; Hofmann, P. A spectroscopic investigation of the adsorption of phenol on Cu(110) Vacuum 1983, 33 (10-1) 793-796
-
(1983)
Vacuum
, vol.33
, Issue.101
, pp. 793-796
-
-
Richardson, N.V.1
Hofmann, P.2
-
32
-
-
34248216076
-
Molecular orbital model for pyridine/alpha-pyridyl adsorption on metal surfaces
-
Jones, T. E.; Zuo, C.; Jagodzinski, P. W.; Eberhart, M. E. Molecular orbital model for pyridine/alpha-pyridyl adsorption on metal surfaces J. Phys. Chem. C 2007, 111 (14) 5493-5496
-
(2007)
J. Phys. Chem. C
, vol.111
, Issue.14
, pp. 5493-5496
-
-
Jones, T.E.1
Zuo, C.2
Jagodzinski, P.W.3
Eberhart, M.E.4
-
33
-
-
0037173310
-
Adlayer structures of pyridine, pyrazine and triazine on Cu(111): An in situ scanning tunneling microscopy study
-
Wang, D.; Xu, Q. M.; Wan, L. J.; Wang, C.; Bai, C. L. Adlayer structures of pyridine, pyrazine and triazine on Cu(111): An in situ scanning tunneling microscopy study Langmuir 2002, 18 (13) 5133-5138
-
(2002)
Langmuir
, vol.18
, Issue.13
, pp. 5133-5138
-
-
Wang, D.1
Xu, Q.M.2
Wan, L.J.3
Wang, C.4
Bai, C.L.5
-
35
-
-
0346749657
-
Renaissance of Ullmann and Goldberg reactions - Progress in copper catalyzed C-N-, C-O-, and C-S-coupling
-
Kunz, K.; Scholz, U.; Ganzer, D. Renaissance of Ullmann and Goldberg reactions-Progress in copper catalyzed C-N-, C-O-, and C-S-coupling Synlett 2003, 2003 (15) 2428-2439
-
(2003)
Synlett
, vol.2003
, Issue.15
, pp. 2428-2439
-
-
Kunz, K.1
Scholz, U.2
Ganzer, D.3
-
36
-
-
36449000663
-
Benzene adsorption on Cu(111) - Formation of a stable bilayer
-
Xi, M.; Yang, M. X.; Jo, S. K.; Bent, B. E.; Stevens, P. Benzene adsorption on Cu(111)-Formation of a stable bilayer J. Chem. Phys. 1994, 101 (10) 9122-9131
-
(1994)
J. Chem. Phys.
, vol.101
, Issue.10
, pp. 9122-9131
-
-
Xi, M.1
Yang, M.X.2
Jo, S.K.3
Bent, B.E.4
Stevens, P.5
-
37
-
-
0029184806
-
The adsorption of pyridine at clean, oxidized and hydroxylated Cu(111) surfaces
-
Davies, P. R.; Shukla, N. The adsorption of pyridine at clean, oxidized and hydroxylated Cu(111) surfaces Surf. Sci. 1995, 322 (1-3) 8-20
-
(1995)
Surf. Sci.
, vol.322
, Issue.13
, pp. 8-20
-
-
Davies, P.R.1
Shukla, N.2
-
38
-
-
84856347507
-
NAr-type C-O coupling reactions
-
NAr-type C-O coupling reactions Chem.-Eur. J. 2012, 18 (6) 1800-1810
-
(2012)
Chem. - Eur. J.
, vol.18
, Issue.6
, pp. 1800-1810
-
-
Benaskar, F.1
Engels, V.2
Rebrov, E.V.3
Patil, N.G.4
Meuldijk, J.5
Magusin, P.C.M.M.6
Mezari, B.7
Hessel, V.8
Hulshof, L.A.9
Thüne, P.C.10
Hensen, E.J.M.11
Wheatley, A.E.H.12
Schouten, J.C.13
-
39
-
-
84860280229
-
Cost analysis for a continuously operated fine chemicals production plant at 10 kg/day using a combination of microprocessing and microwave heating
-
Benaskar, F.; Ben-Abdelmoumen, A.; Patil, N. G.; Rebrov, E. V.; Meuldijk, J.; Hulshof, L. A.; Hessel, V.; Krtschil, U.; Schouten, J. C. Cost analysis for a continuously operated fine chemicals production plant at 10 kg/day using a combination of microprocessing and microwave heating J. Flow Chem. 2011, 1 (2) 74-89
-
(2011)
J. Flow Chem.
, vol.1
, Issue.2
, pp. 74-89
-
-
Benaskar, F.1
Ben-Abdelmoumen, A.2
Patil, N.G.3
Rebrov, E.V.4
Meuldijk, J.5
Hulshof, L.A.6
Hessel, V.7
Krtschil, U.8
Schouten, J.C.9
-
40
-
-
80052103380
-
Aryl-O reductive elimination from reaction of well-defined aryl-CuIII species with phenolates: The importance of ligand reactivity
-
Casitas, A.; Ioannidis, N.; Mitrikas, G.; Costas, M.; Ribas, X. Aryl-O reductive elimination from reaction of well-defined aryl-CuIII species with phenolates: The importance of ligand reactivity Dalton Trans. 2011, 40 (35) 8796-8799
-
(2011)
Dalton Trans.
, vol.40
, Issue.35
, pp. 8796-8799
-
-
Casitas, A.1
Ioannidis, N.2
Mitrikas, G.3
Costas, M.4
Ribas, X.5
-
41
-
-
78049335595
-
Arylation of unactivated arenes
-
Lei, A.; Liu, W.; Liu, C.; Chen, M. Arylation of unactivated arenes Dalton Trans. 2010, 39 (43) 10352-10361
-
(2010)
Dalton Trans.
, vol.39
, Issue.43
, pp. 10352-10361
-
-
Lei, A.1
Liu, W.2
Liu, C.3
Chen, M.4
-
42
-
-
78049346662
-
The mechanism of the modified Ullmann reaction
-
Sperotto, E.; van Klink, G. P. M.; van Koten, G.; de Vries, J. G. The mechanism of the modified Ullmann reaction Dalton Trans. 2010, 39 (43) 10338-10351
-
(2010)
Dalton Trans.
, vol.39
, Issue.43
, pp. 10338-10351
-
-
Sperotto, E.1
Van Klink, G.P.M.2
Van Koten, G.3
De Vries, J.G.4
-
43
-
-
33749129825
-
Complexes of copper(I) with aromatic compounds in aqueous solutions
-
Saphier, M.; Burg, A.; Sheps, S.; Cohen, H.; Meyerstein, D. Complexes of copper(I) with aromatic compounds in aqueous solutions J. Chem. Soc., Dalton Trans. 1999, 11) 1845-1850
-
(1999)
J. Chem. Soc., Dalton Trans.
, Issue.11
, pp. 1845-1850
-
-
Saphier, M.1
Burg, A.2
Sheps, S.3
Cohen, H.4
Meyerstein, D.5
-
44
-
-
0036238145
-
Copper(I) as a homogeneous catalyst for the ullmann reaction in aqueous solutions - The transformation of 2-bromobenzoate into salicylate
-
Saphier, M.; Masarwa, A.; Cohen, H.; Meyerstein, D. Copper(I) as a homogeneous catalyst for the ullmann reaction in aqueous solutions-The transformation of 2-bromobenzoate into salicylate Eur. J. Inorg. Chem. 2002, 2002 (5) 1226-1234
-
(2002)
Eur. J. Inorg. Chem.
, vol.2002
, Issue.5
, pp. 1226-1234
-
-
Saphier, M.1
Masarwa, A.2
Cohen, H.3
Meyerstein, D.4
-
45
-
-
37049084739
-
Kinetics and equilibria of reactions between acetic anhydride and substituted phenolate ions in aqueous and chlorobenzene solutions
-
Ba-Saif, S. A.; Maude, A. B.; Williams, A. Kinetics and equilibria of reactions between acetic anhydride and substituted phenolate ions in aqueous and chlorobenzene solutions J. Chem. Soc., Perkin Trans. 2 1994, 12) 2395-2400
-
(1994)
J. Chem. Soc., Perkin Trans. 2
, Issue.12
, pp. 2395-2400
-
-
Ba-Saif, S.A.1
Maude, A.B.2
Williams, A.3
-
46
-
-
67349180231
-
Highly efficient synthesis of functionalized tertiary alcohols catalyzed by potassium alkoxide-crown ether complexes
-
Hatano, M.; Suzuki, S.; Takagi, E.; Ishihara, K. Highly efficient synthesis of functionalized tertiary alcohols catalyzed by potassium alkoxide-crown ether complexes Tetrahedron Lett. 2009, 50 (26) 3171-3174
-
(2009)
Tetrahedron Lett.
, vol.50
, Issue.26
, pp. 3171-3174
-
-
Hatano, M.1
Suzuki, S.2
Takagi, E.3
Ishihara, K.4
-
47
-
-
13544273190
-
Copper(I)-mediated ligand-accelerated Ullmann-type coupling of anilines with aryliodides: Ligand selection and reaction kinetics for synthesis of tri- p -tolylamine
-
Manifar, T.; Rohani, S.; Bender, T. P.; Goodbrand, H. B.; Gaynor, R.; Saban, M. Copper(I)-mediated ligand-accelerated Ullmann-type coupling of anilines with aryliodides: Ligand selection and reaction kinetics for synthesis of tri- p -tolylamine Ind. Chem. Eng. Res. 2005, 44, 789-798
-
(2005)
Ind. Chem. Eng. Res.
, vol.44
, pp. 789-798
-
-
Manifar, T.1
Rohani, S.2
Bender, T.P.3
Goodbrand, H.B.4
Gaynor, R.5
Saban, M.6
-
48
-
-
0001199033
-
Mechanisms and models for copper mediated nucleophilic aromatic substitution. 2. A single catalytic species from three different oxidation states of copper in an ullmann synthesis of triarylamines
-
Paine, A. J. Mechanisms and models for copper mediated nucleophilic aromatic substitution. 2. A single catalytic species from three different oxidation states of copper in an ullmann synthesis of triarylamines J. Am. Chem. Soc. 1987, 109 (5) 1496-1502
-
(1987)
J. Am. Chem. Soc.
, vol.109
, Issue.5
, pp. 1496-1502
-
-
Paine, A.J.1
-
49
-
-
78049346662
-
The mechanism of the modified Ullmann reaction
-
Sperotto, E.; van Klink, G. P. M.; van Koten, G.; de Vries, J. G. The mechanism of the modified Ullmann reaction Dalton Trans. 2010, 39 (43) 10338-10351
-
(2010)
Dalton Trans.
, vol.39
, Issue.43
, pp. 10338-10351
-
-
Sperotto, E.1
Van Klink, G.P.M.2
Van Koten, G.3
De Vries, J.G.4
|