-
1
-
-
0037007703
-
Ullmann diaryl ether synthesis: Rate acceleration by 2,2,6,6- tetramethylheptane-3,5-dione
-
E. Buck, Z.J. Song, and D. Tschaen et al. Ullmann diaryl ether synthesis: rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione J. Org. Lett. 4 2002 1623 1626
-
(2002)
J. Org. Lett.
, vol.4
, pp. 1623-1626
-
-
Buck, E.1
Song, Z.J.2
Tschaen, D.3
-
2
-
-
34247553656
-
Biologically active compounds from bryophytes
-
Y. Asakawa Biologically active compounds from bryophytes Pure Appl. Chem. 79 2007 557 580
-
(2007)
Pure Appl. Chem.
, vol.79
, pp. 557-580
-
-
Asakawa, Y.1
-
3
-
-
41649095662
-
An efficient intermolecular BINAM-copper (I) catalyzed Ullmann-type coupling of aryl iodides/bromides with aliphatic alcohols
-
A.B. Naidu, and G. Sekar An efficient intermolecular BINAM-copper (I) catalyzed Ullmann-type coupling of aryl iodides/bromides with aliphatic alcohols Tetrahedron Lett. 49 2008 3147 3151
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3147-3151
-
-
Naidu, A.B.1
Sekar, G.2
-
4
-
-
78349298721
-
Synthesis and characterization of polymer anchored Cu(II) complexes: Heterogeneous catalysts for preparation of diaryl ethers
-
M. Islam, S. Mondal, and M. Manir et al. Synthesis and characterization of polymer anchored Cu(II) complexes: heterogeneous catalysts for preparation of diaryl ethers Chin. J. Chem. 28 2010 1810 1820
-
(2010)
Chin. J. Chem.
, vol.28
, pp. 1810-1820
-
-
Islam, M.1
Mondal, S.2
Manir, M.3
-
5
-
-
0020970542
-
A study of ethers for the selection of candidates for carcinogen bioassay
-
C.T. Helmes, C.C. Sigman, and D.L. Atkinson et al. A study of ethers for the selection of candidates for carcinogen bioassay J. Environ. Sci. Health A 18 1983 797 839
-
(1983)
J. Environ. Sci. Health A
, vol.18
, pp. 797-839
-
-
Helmes, C.T.1
Sigman, C.C.2
Atkinson, D.L.3
-
6
-
-
1542527790
-
NAr based macrocyclization via diaryl ether formation: Application in natural product synthesis
-
NAr based macrocyclization via diaryl ether formation: application in natural product synthesis Synlett 2 1997 133 134
-
(1997)
Synlett
, vol.2
, pp. 133-134
-
-
Zhu, J.1
-
7
-
-
2742585020
-
Syntheses of cyclic bisbibenzyl systems
-
T. Eicher, S. Fey, and W. Puhl et al. Syntheses of cyclic bisbibenzyl systems Eur. J. Org. Chem. 1998 1998 877 888
-
(1998)
Eur. J. Org. Chem.
, vol.1998
, pp. 877-888
-
-
Eicher, T.1
Fey, S.2
Puhl, W.3
-
8
-
-
33644802299
-
Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase: Part 2. 2′-Substituted triclosan derivatives
-
J.S. Freundlich, M. Yu, and E. Lucumi et al. Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase: Part 2. 2′-Substituted triclosan derivatives Bioorg. Med. Chem. Lett. 16 2006 2163 2169
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2163-2169
-
-
Freundlich, J.S.1
Yu, M.2
Lucumi, E.3
-
9
-
-
26844461350
-
Synthesis, biological activity, and X-ray crystal structural analysis of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase: Part 1. 4′-Substituted triclosan derivatives
-
J.S. Freundlich, J.W. Anderson, and D. Sarantakis et al. Synthesis, biological activity, and X-ray crystal structural analysis of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase: Part 1. 4′-Substituted triclosan derivatives Bioorg. Med. Chem. Lett. 15 2005 5247 5252
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 5247-5252
-
-
Freundlich, J.S.1
Anderson, J.W.2
Sarantakis, D.3
-
10
-
-
53049101677
-
An efficient Ullmann-Type CO bond formation catalyzed by an air-stable copper(I)-bipyridyl complex
-
J. Niu, H. Zhou, and Z. Li et al. An efficient Ullmann-Type CO bond formation catalyzed by an air-stable copper(I)-bipyridyl complex J. Org. Chem. 73 2008 7814 7817
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7814-7817
-
-
Niu, J.1
Zhou, H.2
Li, Z.3
-
11
-
-
0033549049
-
Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers
-
A. Aranyos, W. David, and A. Kiyomori et al. Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers J. Am. Chem. Soc. 121 1999 4369 4378
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 4369-4378
-
-
Aranyos, A.1
David, W.2
Kiyomori, A.3
-
12
-
-
33747793704
-
The selective reaction of aryl halides with KOH: Synthesis of phenols, aromatic ethers, and benzofurans
-
K.W. Anderson, T. Ikawa, and R.E. Tundel et al. The selective reaction of aryl halides with KOH: synthesis of phenols, aromatic ethers, and benzofurans J. Am. Chem. Soc. 128 2006 10694 10695
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10694-10695
-
-
Anderson, K.W.1
Ikawa, T.2
Tundel, R.E.3
-
13
-
-
84979085204
-
Ueber eine neue Darstellungsweise von Phenyläthersalicylsäure
-
F. Ullmann Ueber eine neue Darstellungsweise von Phenylä thersalicylsäure Ber. Dtsch. Chem. Ges. 37 1904 853 857
-
(1904)
Ber. Dtsch. Chem. Ges.
, vol.37
, pp. 853-857
-
-
Ullmann, F.1
-
14
-
-
34548462479
-
Nitrogen ligands in copper-catalyzed arylation of phenols: Structure/activity relationships and applications
-
A. Ouail, J.F. Spindler, and A. Jutand et al. Nitrogen ligands in copper-catalyzed arylation of phenols: structure/activity relationships and applications Adv. Synth. Catal. 349 2007 1906 1916
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1906-1916
-
-
Ouail, A.1
Spindler, J.F.2
Jutand, A.3
-
15
-
-
0342757538
-
Recent advances in diaryl ether synthesis
-
J.S. Sawyer Recent advances in diaryl ether synthesis Tetrahedron 56 2000 5045 5065
-
(2000)
Tetrahedron
, vol.56
, pp. 5045-5065
-
-
Sawyer, J.S.1
-
16
-
-
0000658001
-
Palladium-catalyzed (Ullmann-type) homocoupling of aryl halides: A convenient and general synthesis of symmetrical biaryls via inter-and intramolecular coupling reactions
-
D.D. Hennings, T. Iwama, and V.H. Rawal Palladium-catalyzed (Ullmann-type) homocoupling of aryl halides: a convenient and general synthesis of symmetrical biaryls via inter-and intramolecular coupling reactions Org. Lett. 1 1999 1205 1208
-
(1999)
Org. Lett.
, vol.1
, pp. 1205-1208
-
-
Hennings, D.D.1
Iwama, T.2
Rawal, V.H.3
-
17
-
-
77953102809
-
A highly active heterogeneous palladium catalyst for the Suzuki-Miyaura and Ullmann coupling reactions of aryl chlorides in aqueous media
-
B. Yuan, Y. Pan, and Y. Li et al. A highly active heterogeneous palladium catalyst for the Suzuki-Miyaura and Ullmann coupling reactions of aryl chlorides in aqueous media Angew. Chem. Int. Ed. 49 2010 4054 4058
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 4054-4058
-
-
Yuan, B.1
Pan, Y.2
Li, Y.3
-
18
-
-
9644277114
-
Copper in cross-coupling reactions: The post-Ullmann chemistry
-
I.P. Beletskaya, and A.V. Cheprakov Copper in cross-coupling reactions: the post-Ullmann chemistry Coord. Chem. Rev. 248 2004 2337 2364
-
(2004)
Coord. Chem. Rev.
, vol.248
, pp. 2337-2364
-
-
Beletskaya, I.P.1
Cheprakov, A.V.2
-
19
-
-
51049092766
-
Copper- or iron-catalyzed arylation of phenols from respectively aryl chlorides and aryl iodides
-
N. Xia, and M. Taillefer Copper- or iron-catalyzed arylation of phenols from respectively aryl chlorides and aryl iodides Chem. Eur. J. 14 2008 6037 6039
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 6037-6039
-
-
Xia, N.1
Taillefer, M.2
-
20
-
-
84878513016
-
Synthesis of 1,7-dimethoxy-2-hydroxyxanthone, a natural product with potential activity on erectile dysfunction
-
W.J. Liu, D.S. Mei, and W.H. Duan Synthesis of 1,7-dimethoxy-2- hydroxyxanthone, a natural product with potential activity on erectile dysfunction Chin. Chem. Lett. 24 2013 515 517
-
(2013)
Chin. Chem. Lett.
, vol.24
, pp. 515-517
-
-
Liu, W.J.1
Mei, D.S.2
Duan, W.H.3
-
21
-
-
84879041469
-
Efficient synthesis of unsymmetrical diaryl thioethers via TBAF-mediated denitrative substitution of nitroarenes with PhSTMS under mild and neutral conditions
-
X.C. Yu, B. Li, and B.H. Yu et al. Efficient synthesis of unsymmetrical diaryl thioethers via TBAF-mediated denitrative substitution of nitroarenes with PhSTMS under mild and neutral conditions Chin. Chem. Lett. 24 2013 605 608
-
(2013)
Chin. Chem. Lett.
, vol.24
, pp. 605-608
-
-
Yu, X.C.1
Li, B.2
Yu, B.H.3
-
22
-
-
47749142816
-
Catalytic CC, CN, and CO Ullmann-type coupling reactions: Copper makes a difference
-
F. Monnier, and M. Taillefer Catalytic CC, CN, and CO Ullmann-type coupling reactions: copper makes a difference Angew. Chem. Int. Ed. 47 2008 3096 3099
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 3096-3099
-
-
Monnier, F.1
Taillefer, M.2
-
23
-
-
36048976987
-
Cu-nanoparticle catalyzed O-arylation of phenols with aryl halides via Ullmann coupling
-
M. Kidwai, N.K. Mishra, and V. Bansal et al. Cu-nanoparticle catalyzed O-arylation of phenols with aryl halides via Ullmann coupling Tetrahedron Lett. 48 2007 8883 8887
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8883-8887
-
-
Kidwai, M.1
Mishra, N.K.2
Bansal, V.3
-
24
-
-
84862822076
-
3 as heterogeneous catalyst for synthesis of diaryl ether under ligand-free conditions
-
3 as heterogeneous catalyst for synthesis of diaryl ether under ligand-free conditions J. Mol. Catal. A: Chem. 357 2012 112 116
-
(2012)
J. Mol. Catal. A: Chem.
, vol.357
, pp. 112-116
-
-
Ling, P.X.1
Li, D.2
Wang, X.Y.3
-
25
-
-
0036589259
-
Arylaryl bond formation one century after the discovery of the Ullmann reaction
-
J. Hassan, M. Sevignon, and C. Gozzi et al. Arylaryl bond formation one century after the discovery of the Ullmann reaction Chem. Rev. 102 2002 1359 1470
-
(2002)
Chem. Rev.
, vol.102
, pp. 1359-1470
-
-
Hassan, J.1
Sevignon, M.2
Gozzi, C.3
-
26
-
-
84857793387
-
Ligand free, highly efficient synthesis of diaryl ether over copper fluorapatite as heterogeneous reusable catalyst
-
S.A.R. Mulla, S.M. Inamdar, and M.Y. Pathan et al. Ligand free, highly efficient synthesis of diaryl ether over copper fluorapatite as heterogeneous reusable catalyst Tetrahedron Lett. 53 2012 1862 1869
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 1862-1869
-
-
Mulla, S.A.R.1
Inamdar, S.M.2
Pathan, M.Y.3
-
27
-
-
84866077880
-
Benzotriazole and its derivatives as ligands in coupling reaction
-
A.K. Verma Benzotriazole and its derivatives as ligands in coupling reaction Adv. Heterocycl. Chem. 107 2012 101 132
-
(2012)
Adv. Heterocycl. Chem.
, vol.107
, pp. 101-132
-
-
Verma, A.K.1
-
28
-
-
84875220599
-
Alkoxylation reactions of aryl halides catalyzed by magnetic copper ferrite
-
S.L. Yang, W.B. Xie, and H. Zhou et al. Alkoxylation reactions of aryl halides catalyzed by magnetic copper ferrite Tetrahedron 69 2013 3415 3418
-
(2013)
Tetrahedron
, vol.69
, pp. 3415-3418
-
-
Yang, S.L.1
Xie, W.B.2
Zhou, H.3
-
29
-
-
84859140879
-
Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids
-
J. Zhang, J. Chen, and M. Liu Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids Green Chem. 14 2012 912 916
-
(2012)
Green Chem.
, vol.14
, pp. 912-916
-
-
Zhang, J.1
Chen, J.2
Liu, M.3
-
30
-
-
84874115728
-
Room temperature Ullmann type CO and CS cross coupling of aryl halides with phenol/thiophenol catalyzed by CuO nanoparticles
-
S.G. Babu, and R. Karvembu Room temperature Ullmann type CO and CS cross coupling of aryl halides with phenol/thiophenol catalyzed by CuO nanoparticles Tetrahedron Lett. 54 2013 1677 1680
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 1677-1680
-
-
Babu, S.G.1
Karvembu, R.2
-
31
-
-
79960160492
-
Impregnated ruthenium on magnetite as a recyclable catalyst for the N-alkylation of amines, sulfonamides, sulfinamides, and nitroarenes using alcohols as electrophiles by a hydrogen autotransfer process
-
R. Cano, D.J. Ramón, and M. Yus Impregnated ruthenium on magnetite as a recyclable catalyst for the N-alkylation of amines, sulfonamides, sulfinamides, and nitroarenes using alcohols as electrophiles by a hydrogen autotransfer process J. Org. Chem. 76 2011 5547 5557
-
(2011)
J. Org. Chem.
, vol.76
, pp. 5547-5557
-
-
Cano, R.1
Ramón, D.J.2
Yus, M.3
-
32
-
-
84855567000
-
Impregnated copper or palladium-copper on magnetite as catalysts for the domino and stepwise Sonogashira-cyclization processes: A straightforward synthesis of benzo[b]furans and indoles
-
R. Cano, M. Yus, and D.J. Ramón Impregnated copper or palladium-copper on magnetite as catalysts for the domino and stepwise Sonogashira-cyclization processes: a straightforward synthesis of benzo[b]furans and indoles Tetrahedron 68 2012 1393 1400
-
(2012)
Tetrahedron
, vol.68
, pp. 1393-1400
-
-
Cano, R.1
Yus, M.2
Ramón, D.J.3
-
33
-
-
84874718066
-
5+δ as cathode material for intermediate temperature solid-oxide fuel cells
-
5+δ as cathode material for intermediate temperature solid-oxide fuel cells J. Power Sources 234 2013 244 251
-
(2013)
J. Power Sources
, vol.234
, pp. 244-251
-
-
Jin, F.F.1
Shen, Y.2
Wang, R.3
|