-
1
-
-
38949179884
-
Electrical properties of layered perovskite-type palladium oxides
-
S. Ayukawa, M. Kato, T. Noji, and Y. Koikea, Electrical properties of layered perovskite-type palladium oxides. Mater. Sci. Eng. B 148, 65 (2008).
-
(2008)
Mater. Sci. Eng. B
, vol.148
, pp. 65
-
-
Ayukawa, S.1
Kato, M.2
Noji, T.3
Koikea, Y.4
-
2
-
-
58149144579
-
Synthesis, structural, magnetic and transport properties of layered perovskite-related titanates, niobates and tantalates of the type A(n)B(n)O(3n + 2), A'A(k - 10B(k)O(3k + 1) and A(m)B(m-1)O(3m)
-
F. Lichtenberg, A. Herrnberger, and K. Wiedenmann, Synthesis, structural, magnetic and transport properties of layered perovskite-related titanates, niobates and tantalates of the type A(n)B(n)O(3n + 2), A'A(k - 10B(k)O(3k + 1) and A(m)B(m-1)O(3m). Prog. Solid State Chem. 36, 253 (2008).
-
(2008)
Prog. Solid State Chem.
, vol.36
, pp. 253
-
-
Lichtenberg, F.1
Herrnberger, A.2
Wiedenmann, K.3
-
3
-
-
84871490291
-
Resistance degradation in donor-doped PZT ceramic stacks with Ag/Pd electrodes: I. Phenomenology of processes
-
L. Andrejs and J. Fleig, Resistance degradation in donor-doped PZT ceramic stacks with Ag/Pd electrodes: I. Phenomenology of processes. J. Eur. Ceram. Soc. 33, 779 (2013).
-
(2013)
J. Eur. Ceram. Soc.
, vol.33
, pp. 779
-
-
Andrejs, L.1
Fleig, J.2
-
4
-
-
44549086574
-
Diesel fuel reforming using catalytic membrane reactors
-
M. V. Mundschau, C. G. Burk, and D. A. Gribble, Jr, Diesel fuel reforming using catalytic membrane reactors. Catal. Today 136, 190 (2008).
-
(2008)
Catal. Today
, vol.136
, pp. 190
-
-
Mundschau, M.V.1
Burk, C.G.2
Gribble, Jr.D.A.3
-
6
-
-
0037567282
-
12
-
12. Chem. Mater. 15, 2193 (2003).
-
(2003)
Chem. Mater.
, vol.15
, pp. 2193
-
-
Sanchez-Benitez, J.1
Alonso, J.A.2
Martinez-Lope, M.J.3
Casais, M.T.4
Martinez, J.L.5
De Andres, A.6
Fernandez-Diaz, M.T.7
-
7
-
-
33748758704
-
Self-regenerating Rh and Pt-based perovskite catalysts for automotive-emissions control
-
H. Tanaka, M. Taniguchi, M. Uenishi, N. Kajita, I. Tan, Y. Nishihata, J. Mizuki, K. Narita, M. Kimura, and K. Kaneko, Self-regenerating Rh- and Pt-based perovskite catalysts for automotive-emissions control. Angew. Chem. Int. Ed. 45, 5998 (2006).
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5998
-
-
Tanaka, H.1
Taniguchi, M.2
Uenishi, M.3
Kajita, N.4
Tan, I.5
Nishihata, Y.6
Mizuki, J.7
Narita, K.8
Kimura, M.9
Kaneko, K.10
-
8
-
-
77950278574
-
Strontium-doped perovskites rival platinum catalysts for treating NOx in simulated diesel exhaust
-
C. H. Kim, G. Qi, K. Dahlberg, and W. Li, Strontium-doped perovskites rival platinum catalysts for treating NOx in simulated diesel exhaust. Science 327, 1624 (2010).
-
(2010)
Science
, vol.327
, pp. 1624
-
-
Kim, C.H.1
Qi, G.2
Dahlberg, K.3
Li, W.4
-
9
-
-
76649098013
-
3 electrolyte with novel Pr2NiO4 cathode
-
3 electrolyte with novel Pr2NiO4 cathode. Fuel Cells 10, 166 (2010).
-
(2010)
Fuel Cells
, vol.10
, pp. 166
-
-
Taillades, G.1
Dailly, J.2
Taillades-Jacquin, M.3
Mauvy, F.4
Essoumhi, A.5
Marrony, M.6
Lalanne, C.7
Fourcade, S.8
Jones, D.J.9
Grenier, J.-C.10
Roziére, J.11
-
10
-
-
56949096916
-
Synthesis and characterization of Ni-cermet/proton conducting thin film electrolyte symmetrical assemblies
-
A. Essoumhi, G. Taillades, M. Taillades-Jacquin, D. J. Jones, and J. Roziére, Synthesis and characterization of Ni-cermet/proton conducting thin film electrolyte symmetrical assemblies. Solid State Ionics 179, 2155 (2008).
-
(2008)
Solid State Ionics
, vol.179
, pp. 2155
-
-
Essoumhi, A.1
Taillades, G.2
Taillades-Jacquin, M.3
Jones, D.J.4
Roziére, J.5
-
11
-
-
71749095989
-
Perovskite-type mixed oxides as catalytic material for NO removal
-
J. Zhu and A. Thomas, Perovskite-type mixed oxides as catalytic material for NO removal. Appl. Catal. B-Environ. 92, 225 (2009).
-
(2009)
Appl. Catal. B-Environ.
, vol.92
, pp. 225
-
-
Zhu, J.1
Thomas, A.2
-
12
-
-
33646806480
-
Oxidation of CO over Ru containing perovskite type oxides
-
S. Petrovic, V. Rakic, D. M. Jovanovic, and A. T. Baricevic, Oxidation of CO over Ru containing perovskite type oxides. Appl. Catal. B-Environ. 66, 249 (2006).
-
(2006)
Appl. Catal. B-Environ.
, vol.66
, pp. 249
-
-
Petrovic, S.1
Rakic, V.2
Jovanovic, D.M.3
Baricevic, A.T.4
-
13
-
-
34347338603
-
3-delta, for CO oxidation
-
3-delta, for CO oxidation. J. Catal. 249, 349 (2007).
-
(2007)
J. Catal.
, vol.249
, pp. 349
-
-
Singh, U.G.1
Li, J.2
Bennett, J.W.3
Rappe, A.M.4
Seshadri, R.5
Scott, S.L.6
-
14
-
-
33746986031
-
Fe-based perovskites substituted by copper and palladium for NO+CO reaction
-
R. Zhang, H. Alamdari, and S. Kaliaguine, Fe-based perovskites substituted by copper and palladium for NO+CO reaction. J. Catal. 242, 241 (2006).
-
(2006)
J. Catal.
, vol.242
, pp. 241
-
-
Zhang, R.1
Alamdari, H.2
Kaliaguine, S.3
-
15
-
-
34548438382
-
Studies of the activation process over Pd perovskite-type oxides used for catalytic oxidation of toluene
-
J.-M. Giraudon, A. Elhachimi, F. Wyrwalsky, S. Siffert, A. Aboukais, J.-F. Lamonier, and G. Leclercq, Studies of the activation process over Pd perovskite-type oxides used for catalytic oxidation of toluene. Appl. Catal. B-Environ. 75, 157 (2007).
-
(2007)
Appl. Catal. B-Environ.
, vol.75
, pp. 157
-
-
Giraudon, J.-M.1
Elhachimi, A.2
Wyrwalsky, F.3
Siffert, S.4
Aboukais, A.5
Lamonier, J.-F.6
Leclercq, G.7
-
16
-
-
33748466901
-
-3 monolithic catalysts for the combustion of methane under fuel-rich conditions
-
-3 monolithic catalysts for the combustion of methane under fuel-rich conditions. Catal. Today 117, 454 (2006).
-
(2006)
Catal. Today
, vol.117
, pp. 454
-
-
Cimino, S.1
Landi, G.2
Lisi, L.3
Russo, G.4
-
17
-
-
84876252203
-
Photocatalytic decomposition of methyl orange over nanosized perovskite-type oxides under visible light irradiation
-
M. W. Ha, W. Y. Jung, K. T. Lim, M. S. Lee, and S. S. Hong, Photocatalytic decomposition of methyl orange over nanosized perovskite-type oxides under visible light irradiation. J. Nanosci. Nanotechnol. 13, 2330 (2013).
-
(2013)
J. Nanosci. Nanotechnol.
, vol.13
, pp. 2330
-
-
Ha, M.W.1
Jung, W.Y.2
Lim, K.T.3
Lee, M.S.4
Hong, S.S.5
-
19
-
-
0011717658
-
Selective catalytic activity reduction of NOx with N-free reductants
-
M. Shelef, Selective catalytic activity reduction of NOx with N-free reductants. Chem. Rev. 95, 209 (1995).
-
(1995)
Chem. Rev.
, vol.95
, pp. 209
-
-
Shelef, M.1
-
20
-
-
0028768016
-
Selective reduction of NO by hydrocarbons and oxygenated hydrocarbons over metal-oxides catalysts
-
H. Hamada, Selective reduction of NO by hydrocarbons and oxygenated hydrocarbons over metal-oxides catalysts. Catal. Today 22, 21 (1994).
-
(1994)
Catal. Today
, vol.22
, pp. 21
-
-
Hamada, H.1
-
21
-
-
0001370131
-
Selective reduction of nitrogenoxides by hydrocarbons under lear-burn conditions using supported ptatinium-group metal-catalysts
-
R. Burch and P. J. Millington, Selective reduction of nitrogenoxides by hydrocarbons under Lear-Burn conditions using supported ptatinium-group metal-catalysts. Catal. Today 26, 185 (1995).
-
(1995)
Catal. Today
, vol.26
, pp. 185
-
-
Burch, R.1
Millington, P.J.2
-
22
-
-
84876245602
-
Influence of a surfactant and reducing agent on preparation of palladium
-
S. C. Kim, S. C. Jung, Y. K. Park, H. G. Ahn, and S. G. Seo, Influence of a surfactant and reducing agent on preparation of palladium. J. Nanosci. Nanotechnol. 13, 1961 (2013).
-
(2013)
J. Nanosci. Nanotechnol.
, vol.13
, pp. 1961
-
-
Kim, S.C.1
Jung, S.C.2
Park, Y.K.3
Ahn, H.G.4
Seo, S.G.5
-
23
-
-
33749515284
-
Recent advances in Pd/C-catalyzed coupling reactions
-
M. Seki, Recent advances in Pd/C-catalyzed coupling reactions. Synthesis 2975 (2006).
-
(2006)
Synthesis
, vol.2975
-
-
Seki, M.1
-
24
-
-
0035948250
-
Heterogeneous Heck reaction catalyzed by Pd/C in ionic liquid
-
H. Hagiwara, Y. Shimizu, T. Hoshi, T. Suzuki, M. Ando, K. Ohkubo, and C. Yokoyama, Heterogeneous Heck reaction catalyzed by Pd/C in ionic liquid. Tetrahedron Lett. 42, 4349 (2001).
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4349
-
-
Hagiwara, H.1
Shimizu, Y.2
Hoshi, T.3
Suzuki, T.4
Ando, M.5
Ohkubo, K.6
Yokoyama, C.7
-
25
-
-
0034689553
-
Palladium-catalyzed homogeneous and heterogeneous Heck reactions in NMP and water-mixed solvents using organic, inorganic and mixed bases
-
F. Zhao, M. Shirai, and M. Arai, Palladium-catalyzed homogeneous and heterogeneous Heck reactions in NMP and water-mixed solvents using organic, inorganic and mixed bases. J. Mol. Catal. A: Chem. 154, 39 (2000).
-
(2000)
J. Mol. Catal. A: Chem.
, vol.154
, pp. 39
-
-
Zhao, F.1
Shirai, M.2
Arai, M.3
-
27
-
-
0032477347
-
Heterogeneous Heck catalysis with palladium-grafted molecular sieves
-
C. P. Mehnert, D. W. Weaver, and J. Y. Ying, Heterogeneous Heck catalysis with palladium-grafted molecular sieves. J. Am. Chem. Soc. 120, 12289 (1998).
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 12289
-
-
Mehnert, C.P.1
Weaver, D.W.2
Ying, J.Y.3
-
28
-
-
0034832488
-
Heck reaction catalyzed by Pdmodified zeolites
-
L. Djakovitch and K. Koehler, Heck reaction catalyzed by Pdmodified zeolites. J. Am. Chem. Soc. 123, 5990 (2001).
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5990
-
-
Djakovitch, L.1
Koehler, K.2
-
29
-
-
0035029450
-
Metallic palladium in the Heck reaction: Active catalyst or convenient precursor?
-
A. Biffis, M. Zecca, and M. Basato, Metallic palladium in the Heck reaction: Active catalyst or convenient precursor? Eur. J. Inorg. Chem. 1131 (2001).
-
(2001)
Eur. J. Inorg. Chem.
, vol.1131
-
-
Biffis, A.1
Zecca, M.2
Basato, M.3
-
30
-
-
0034253330
-
Heck reactions catalyzed by oxide-supported palladiumstructure- activity relationships
-
M. Wagner, K. Köhler, L. Djakovitch, S. Weinkauf, V. Hagen, and M. Muhler, Heck reactions catalyzed by oxide-supported palladiumstructure- activity relationships. Top. Catal. 13, 319 (2000).
-
(2000)
Top. Catal.
, vol.13
, pp. 319
-
-
Wagner, M.1
Köhler, K.2
Djakovitch, L.3
Weinkauf, S.4
Hagen, V.5
Muhler, M.6
-
31
-
-
0035866481
-
Supported palladium as catalyst for carbon-carbon bond construction (Heck reaction) in organic synthesis
-
K. Köhler, M. Wagner, and L. Djakovitch, Supported palladium as catalyst for carbon-carbon bond construction (Heck reaction) in organic synthesis. Catal. Today 66, 105 (2001).
-
(2001)
Catal. Today
, vol.66
, pp. 105
-
-
Köhler, K.1
Wagner, M.2
Djakovitch, L.3
-
32
-
-
0002569103
-
Pd-Cu-exchanged montmorillonite K10 clay: An efficient and reusable heterogeneous catalyst for vinylation of aryl halides
-
R. K. Ramchandani, B. S. Uphade, M. P. Vinod, R. D. Wakharkar, V. R. Choudhary, and A. Sudalai, Pd-Cu-exchanged montmorillonite K10 clay: an efficient and reusable heterogeneous catalyst for vinylation of aryl halides. Chem. Commun. 2071 (1997).
-
(1997)
Chem. Commun.
, vol.2071
-
-
Ramchandani, R.K.1
Uphade, B.S.2
Vinod, M.P.3
Wakharkar, R.D.4
Choudhary, V.R.5
Sudalai, A.6
-
33
-
-
0033548447
-
Palladium chloride and tetraphenylphosphonium bromide intercalated clay as a new catalyst for the heck reaction
-
R. S. Varma, K. P. Naicker, and P. J. Liesen, Palladium chloride and tetraphenylphosphonium bromide intercalated clay as a new catalyst for the Heck reaction. Tetrahedron Lett. 40, 2075 (1999).
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 2075
-
-
Varma, R.S.1
Naicker, K.P.2
Liesen, P.J.3
-
34
-
-
0000849514
-
The use of palladium on porous glass for catalytic coupling reactions
-
J. Li, A. W. H. Mau, and C. R. Strauss, The use of palladium on porous glass for catalytic coupling reactions. Chem. Commun. 1275 (1997).
-
(1997)
Chem. Commun.
, vol.1275
-
-
Li, J.1
Mau, A.W.H.2
Strauss, C.R.3
-
35
-
-
4544298371
-
Development of a continuous-flow system for catalysis with palladium(O) particles
-
W. Solodenko, H. Wen, S. Leue, F. Stuhlmann, G. Sourkouni- Argirusi, G. Jas, H. Schönfeld, U. Kunz, and A. Kirschning, Development of a continuous-flow system for catalysis with palladium(O) particles. Eur. J. Org. Chem. 3601 (2004).
-
(2004)
Eur. J. Org. Chem.
, vol.3601
-
-
Solodenko, W.1
Wen, H.2
Leue, S.3
Stuhlmann, F.4
Sourkouni-Argirusi, G.5
Jas, G.6
Schönfeld, H.7
Kunz, U.8
Kirschning, A.9
-
36
-
-
0035840198
-
Palladium metal catalysts in Heck C-C coupling reactions
-
A. Biffis, M. Zecca, and M. Basato, Palladium metal catalysts in Heck C-C coupling reactions. J. Mol. Catal. A: Chem. 173, 249 (2001).
-
(2001)
J. Mol. Catal. A: Chem.
, vol.173
, pp. 249
-
-
Biffis, A.1
Zecca, M.2
Basato, M.3
-
37
-
-
13844280111
-
Self-regeneration of palladium-perovskite catalysts in modem automobiles
-
Y. Nishihata, J. Mizuki, H. Tanaka, M. Uenishi, and M. Kimura, Self-regeneration of palladium-perovskite catalysts in modem automobiles. J. Phys. Chem. Solids 66, 274 (2005).
-
(2005)
J. Phys. Chem. Solids
, vol.66
, pp. 274
-
-
Nishihata, Y.1
Mizuki, J.2
Tanaka, H.3
Uenishi, M.4
Kimura, M.5
-
38
-
-
33748208335
-
Intelligent catalyst having the self-regenerative function of pd rh and pt for automotive emissions control
-
H. Tanaka, M. Uenishi, M. Taniguchi, I. Tan, K. Narita, M. Kimura, K. Kaneko, Y. Nishihata, and J. Mizuki, Intelligent catalyst having the self-regenerative function of Pd, Rh and Pt for automotive emissions control. Catal. Today 117, 321 (2006).
-
(2006)
Catal. Today
, vol.117
, pp. 321
-
-
Tanaka, H.1
Uenishi, M.2
Taniguchi, M.3
Tan, I.4
Narita, K.5
Kimura, M.6
Kaneko, K.7
Nishihata, Y.8
Mizuki, J.9
-
39
-
-
0037062941
-
Self-regeneration of a Pd-perovskite catalyst for automotive emissions control
-
Y. Nishihata, J. Mizuki, T. Akao, H. Tanaka, M. Uenishi, M. Kimura, T. Okamoto, and N. Hamada, Self-regeneration of a Pd-perovskite catalyst for automotive emissions control. Nature 418, 164 (2002).
-
(2002)
Nature
, vol.418
, pp. 164
-
-
Nishihata, Y.1
Mizuki, J.2
Akao, T.3
Tanaka, H.4
Uenishi, M.5
Kimura, M.6
Okamoto, T.7
Hamada, N.8
-
40
-
-
17844380034
-
Redox behavior of palladium at startup in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function
-
M. Uenishia, M. Taniguchi, H. Tanaka, M. Kimura, Y. Nishihata, J. Mizuki, and T. Kobayashie, Redox behavior of palladium at startup in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function. Appl. Catal. B-Environ. 57, 267 (2005).
-
(2005)
Appl. Catal. B-Environ.
, vol.57
, pp. 267
-
-
Uenishia, M.1
Taniguchi, M.2
Tanaka, H.3
Kimura, M.4
Nishihata, Y.5
Mizuki, J.6
Kobayashie, T.7
-
41
-
-
0037696375
-
2
-
2. Appl. Catal. B-Environ. 42, 251 (2003).
-
(2003)
Appl. Catal. B-Environ.
, vol.42
, pp. 251
-
-
Morato, A.1
Medin, F.2
Sueiras, J.E.3
Cesteros, Y.4
Salagre, P.5
De Ménorval, L.C.6
Tichit, D.7
Coq, B.8
-
42
-
-
84861364957
-
-3 +/-delta (A = La, Y; B = Mn, Fe, Co)
-
-3 +/-delta (A = La, Y; B = Mn, Fe, Co). Chem. Mater. 24, 1864 (2012).
-
(2012)
Chem. Mater.
, vol.24
, pp. 1864
-
-
Eyssler, A.1
Winkler, A.2
Safonova, O.3
Nachtegaal, M.4
Matam, S.K.5
Hug, P.6
Weidenkaff, A.7
Ferri, D.8
-
44
-
-
40849083363
-
3 perovskite catalysts on ceramic and metallic monoliths: Physico-chemical characterization and catalytic activity in methane combustion
-
3 perovskite catalysts on ceramic and metallic monoliths: Physico-chemical characterization and catalytic activity in methane combustion. Appl. Catal. A-Gen. 339, 1 (2008).
-
(2008)
Appl. Catal. A-Gen.
, vol.339
, pp. 1
-
-
Arendt, E.1
Maione, A.2
Klisinska, A.3
Sanz, O.4
Montes, M.5
Suarez, S.6
Blanco, J.7
Ruiz, P.8
-
45
-
-
48049090695
-
3-based catalysts for methane combustion
-
3-based catalysts for methane combustion. Catal. Today 137, 318 (2008).
-
(2008)
Catal. Today
, vol.137
, pp. 318
-
-
Kucharczyk, B.1
Tylus, W.2
-
47
-
-
79955409892
-
Perovskite oxide nanowires: Syn thesis, property and structural characterization
-
X. Zhu, Z. Liu, and N. Ming, Perovskite oxide nanowires: synthesis, property and structural characterization. J. Nanosci. Nanotechol. 10, 4109 (2010).
-
(2010)
J. Nanosci. Nanotechol.
, vol.10
, pp. 4109
-
-
Zhu, X.1
Liu, Z.2
Ming, N.3
-
48
-
-
31144477485
-
3 perovskite automotive catalyst having a self-regenerative function
-
3 perovskite automotive catalyst having a self-regenerative function. J. Alloys Compd. 408-412, 1071 (2006).
-
(2006)
J. Alloys Compd.
, vol.408-412
, pp. 1071
-
-
Tanaka, H.1
Tan, I.2
Uenishi, M.3
Taniguchi, M.4
Kimura, M.5
Nishihata, Y.6
Mizuki, J.7
-
50
-
-
27744470887
-
The reducing capability of palladium segregated from perovskite-type LaFePdOx automotive catalysts
-
M. Uenishi, H. Tanaka, M. Taniguchi, I. Tan, Y. Sakamoto, S. Matsunaga, K. Yokota, and T. Kobayashi, The reducing capability of palladium segregated from perovskite-type LaFePdOx automotive catalysts. Appl. Catal. A-Gen. 296, 114 (2005).
-
(2005)
Appl. Catal. A-Gen.
, vol.296
, pp. 114
-
-
Uenishi, M.1
Tanaka, H.2
Taniguchi, M.3
Tan, I.4
Sakamoto, Y.5
Matsunaga, S.6
Yokota, K.7
Kobayashi, T.8
-
55
-
-
53949100646
-
Preparation, active phase composition and Pd content of perovskitetype oxides
-
E. Tzimpilis, N. Moschoudis, M. Stoukides, and P. Bekiaroglou, Preparation, active phase composition and Pd content of perovskitetype oxides. Appl. Catal. B-Environ. 84, 607 (2008).
-
(2008)
Appl. Catal. B-Environ.
, vol.84
, pp. 607
-
-
Tzimpilis, E.1
Moschoudis, N.2
Stoukides, M.3
Bekiaroglou, P.4
-
56
-
-
73649115997
-
Elucidation of structure-activity relationships of model three way catalysts for the combustion of methane
-
X. Wei, P. Hug, R. Figi, M. Trottmann, A. Weidenkaff, and D. Ferri, Elucidation of structure-activity relationships of model three way catalysts for the combustion of methane. Appl. Catal. B-Environ. 94, 27 (2010).
-
(2010)
Appl. Catal. B-Environ.
, vol.94
, pp. 27
-
-
Wei, X.1
Hug, P.2
Figi, R.3
Trottmann, M.4
Weidenkaff, A.5
Ferri, D.6
-
57
-
-
36048936406
-
3-supported Pd: 1. Structure, thermal stability and reducibility
-
3-supported Pd: 1. Structure, thermal stability and reducibility. J. Catal. 252, 127 (2007).
-
(2007)
J. Catal.
, vol.252
, pp. 127
-
-
Chiarello, G.L.1
Grunwaldt, J.D.2
Ferri, D.3
Krumeich, F.4
Oliva, C.5
Forni, L.6
Baiker, A.7
-
58
-
-
84894108155
-
-
Institute of Technology, Nirma University, Ahmedabad
-
D. Tank, F. Panel, and S. Patel, Review Paper on Perovskite Prepared by Reactive Grinding, Institute of Technology, Nirma University, Ahmedabad (2011), Vol. 382, p. 481 .
-
(2011)
Review Paper on Perovskite Prepared by Reactive Grinding
, vol.382
, pp. 481
-
-
Tank, D.1
Panel, F.2
Patel, S.3
-
59
-
-
30144442157
-
Cuand Pd-substituted nanoscale Fe-based perovskites for selective catalytic reduction of NO by propene
-
R. Zhang, A. Villanueva, H. Alamdari, and S. Kaliaguine, Cuand Pd-substituted nanoscale Fe-based perovskites for selective catalytic reduction of NO by propene. J. Catal. 237, 368 (2006).
-
(2006)
J. Catal.
, vol.237
, pp. 368
-
-
Zhang, R.1
Villanueva, A.2
Alamdari, H.3
Kaliaguine, S.4
-
63
-
-
84894134143
-
-
L. Weng, G. Deyong, and X. Xin, China Pertoleum and Petrochemical Technology, 14, 1 (2012).
-
(2012)
China Pertoleum and Petrochemical Technology
, vol.14
, pp. 1
-
-
Weng, L.1
Deyong, G.2
Xin, X.3
-
64
-
-
3142772702
-
3 perovskites for catalytic combustion of methane
-
3 perovskites for catalytic combustion of methane. Catal. Today 90, 121 (2004).
-
(2004)
Catal. Today
, vol.90
, pp. 121
-
-
Kucharczyk, B.1
Tylus, W.2
-
66
-
-
80052261515
-
Pd-integrated lanthanumtransition metal perovskites for methanol partial oxidation
-
C.-L. Li, C.-L. Wang, and Y.-C. Lin, Pd-integrated lanthanumtransition metal perovskites for methanol partial oxidation. Catal. Today 174, 135 (2011).
-
(2011)
Catal. Today
, vol.174
, pp. 135
-
-
Li, C.-L.1
Wang, C.-L.2
Lin, Y.-C.3
-
68
-
-
84862065162
-
Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel prize
-
C. C. C. J. Seechurn, M. O. Kitching, T. J. Colacot, and V. Snieckus, Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel prize. Angew. Chem. Int. Ed. 51, 5062 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 5062
-
-
Seechurn, C.C.C.J.1
Kitching, M.O.2
Colacot, T.J.3
Snieckus, V.4
-
69
-
-
84878638599
-
Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: A remarkable advance from palladium to nickel catalysts
-
F.-S. Han, Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: a remarkable advance from palladium to nickel catalysts. Chem. Soc. Rev. 42, 5270 (2013).
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 5270
-
-
Han, F.-S.1
-
70
-
-
0001758225
-
Theoretical studies in palladium and platinum molecular chemistry
-
A. Dedieu, Theoretical studies in palladium and platinum molecular chemistry. Chem. Rev. 100, 543 (2000).
-
(2000)
Chem. Rev.
, vol.100
, pp. 543
-
-
Dedieu, A.1
-
71
-
-
77349109953
-
Emergence of palladium (IV) chemistry in synthesis and catalysis
-
P. Sehnal, R. J. K. Taylor, and I. J. S. Fairlamb, Emergence of palladium (IV) chemistry in synthesis and catalysis. Chem. Rev. 110, 824 (2010).
-
(2010)
Chem. Rev.
, vol.110
, pp. 824
-
-
Sehnal, P.1
Taylor, R.J.K.2
Fairlamb, I.J.S.3
-
72
-
-
4043123499
-
Enantioselective palladiumcatalyzed transformations
-
L. F. Tietze, H. Ila, and H. P. Bell, Enantioselective palladiumcatalyzed transformations. Chem. Rev. 104, 3453 (2004).
-
(2004)
Chem. Rev.
, vol.104
, pp. 3453
-
-
Tietze, L.F.1
Ila, H.2
Bell, H.P.3
-
73
-
-
79954531716
-
Palladium(II)-catalyzed alkene functionalization via nucleopalladation: Stereochemical pathways and enantioselective catalytic applications
-
R. I. McDonald, G. Liu, and S. S. Stahl, Palladium(II)-catalyzed alkene functionalization via nucleopalladation: Stereochemical pathways and enantioselective catalytic applications. Chem. Rev. 111, 2981 (2011).
-
(2011)
Chem. Rev.
, vol.111
, pp. 2981
-
-
McDonald, R.I.1
Liu, G.2
Stahl, S.S.3
-
74
-
-
84875818323
-
Enantioselective palladium-catalyzed decarboxylative allylation of carbazolones: Total synthesis of (-)-aspidospermidine and (+)-kopsihainanine A
-
Z. Q. Li, S. X. Zhang, S. T. Wu, X. L. Shen, L. W. Zou, F. Q. Wang, X. Li, F. Z. Peng, H. B. Zhang, and Z. H. Shao, Enantioselective palladium-catalyzed decarboxylative allylation of carbazolones: total synthesis of (-)-aspidospermidine and (+)-kopsihainanine A. Angw. Chem. Int. Ed. 52, 4117 (2013).
-
(2013)
Angw. Chem. Int. Ed.
, vol.52
, pp. 4117
-
-
Li, Z.Q.1
Zhang, S.X.2
Wu, S.T.3
Shen, X.L.4
Zou, L.W.5
Wang, F.Q.6
Li, X.7
Peng, F.Z.8
Zhang, H.B.9
Shao, Z.H.10
-
75
-
-
33846918696
-
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
-
D. Alberico, M. E. Scott, and M. Lautens, Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Chem. Rev. 107, 174 (2007).
-
(2007)
Chem. Rev.
, vol.107
, pp. 174
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
76
-
-
77349104061
-
Transition metal-catalyzed direct arylation of substrates with activated sp (3)-hybridized C H bonds and some of their synthetic equivalents with aryl halides and pseudohalides
-
F. Bellina and R. Rossi, Transition metal-catalyzed direct arylation of substrates with activated sp(3)-hybridized C H bonds and some of their synthetic equivalents with aryl halides and pseudohalides. Chem. Rev. 110, 1082 (2010).
-
(2010)
Chem. Rev.
, vol.110
, pp. 1082
-
-
Bellina, F.1
Rossi, R.2
-
77
-
-
33751424969
-
Synthesis of heterocycles via palladiumcatalyzed oxidative addition
-
G. Zeni and R. C. Larock, Synthesis of heterocycles via palladiumcatalyzed oxidative addition. Chem. Rev. 106, 4644 (2006).
-
(2006)
Chem. Rev.
, vol.106
, pp. 4644
-
-
Zeni, G.1
Larock, R.C.2
-
78
-
-
80054999158
-
Palladium-catalysed hydroxylation and alkoxylation
-
S. Enthaler and A. Company, Palladium-catalysed hydroxylation and alkoxylation. Chem. Soc. Rev. 40, 4912 (2011).
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4912
-
-
Enthaler, S.1
Company, A.2
-
79
-
-
84872246718
-
Synthesis of heterocycles via palladium-catalyzed carbonylations
-
X.-F. Wu, H. Neumann, and M. Beller, Synthesis of heterocycles via palladium-catalyzed carbonylations. Chem. Rev. 113, 1 (2013).
-
(2013)
Chem. Rev.
, vol.113
, pp. 1
-
-
Wu, X.-F.1
Neumann, H.2
Beller, M.3
-
80
-
-
84866742794
-
Recent applications of the Suzuki reaction in total synthesis
-
M. M. Heravi and E. Hashemi, Recent applications of the Suzuki reaction in total synthesis. Tetraherdon, 68, 9145 (2012).
-
(2012)
Tetraherdon
, vol.68
, pp. 9145
-
-
Heravi, M.M.1
Hashemi, E.2
-
81
-
-
84877577341
-
Palladium-mediated total synthesis of bioactive natural products
-
K. C. Majumdar and B. Sinha, Palladium-mediated total synthesis of bioactive natural products. Synthesis 45, 1271 (2013).
-
(2013)
Synthesis
, vol.45
, pp. 1271
-
-
Majumdar, K.C.1
Sinha, B.2
-
82
-
-
84874886242
-
Total synthesis of linoxepin through a palladiumcatalyzed domino reaction
-
L. F. Tietze, S. C. Duefert, J. M. Clerc, M. C. Bischoff, and D. Stalke, Total synthesis of linoxepin through a palladiumcatalyzed domino reaction. Angw. Chem. Int. Ed. 52, 3192 (2013).
-
(2013)
Angw. Chem. Int. Ed.
, vol.52
, pp. 3192
-
-
Tietze, L.F.1
Duefert, S.C.2
Clerc, J.M.3
Bischoff, M.C.4
Stalke, D.5
-
84
-
-
84856937741
-
An efficient mixed-ligand Pd catalytic system to promote C-N coupling for the synthesis of N-arylaminotriazole nucleosides
-
Y. Fan, Y. Xia, J. Tang, F. Ziarelli, F. Qu, P. Rocchi, J. L. Iovanna, and L. Peng, An efficient mixed-ligand Pd catalytic system to promote C-N coupling for the synthesis of N-arylaminotriazole nucleosides. Chem. Eur. J. 18, 2221 (2012).
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 2221
-
-
Fan, Y.1
Xia, Y.2
Tang, J.3
Ziarelli, F.4
Qu, F.5
Rocchi, P.6
Iovanna, J.L.7
Peng, L.8
-
85
-
-
80051754936
-
General and modular synthesis of isomeric 5-substituted pyridin-2-yl and 6-substituted pyridin-3-yl C-ribonucleosides bearing diverse alkyl, aryl, hetaryl, amino, carbamoyl, and hydroxy groups
-
M. Štefko, L. Slavětínská B. Klepetářová and M. Hocek, General and modular synthesis of isomeric 5-substituted pyridin-2-yl and 6-substituted pyridin-3-yl C-ribonucleosides bearing diverse alkyl, aryl, hetaryl, amino, carbamoyl, and hydroxy groups. J. Org. Chem. 76, 6619 (2011).
-
(2011)
J. Org. Chem.
, vol.76
, pp. 6619
-
-
Štefko, M.1
Slavětínská, L.2
Klepetá řová, B.3
Hocek, M.4
-
86
-
-
84875952816
-
Palladiumcatalyzed oxidative insertion of carbon monoxide to N-sulfonyl-2- aminobiaryls through C H bond activation: Access to bioactive phenanthridinone derivatives in one pot
-
V. Rajeshkumar, T. H. Lee, and S. C. Chuang, Palladiumcatalyzed oxidative insertion of carbon monoxide to N-sulfonyl-2- aminobiaryls through C H bond activation: Access to bioactive phenanthridinone derivatives in one pot. Org. Lett. 15, 1468 (2013).
-
(2013)
Org. Lett.
, vol.15
, pp. 1468
-
-
Rajeshkumar, V.1
Lee, T.H.2
Chuang, S.C.3
-
87
-
-
80052922538
-
Design and synthesis of 2- phenylimidazo[1,2-A]pyridines as a novel class of melatonin receptor ligands
-
S. El Kazzouli, A. G. du Bellay, S. Berteina-Raboin, P. Delagrange, D. H. Caignard, and G. Guillaumet, Design and synthesis of 2- phenylimidazo[1,2-A] pyridines as a novel class of melatonin receptor ligands. Eur. J. Med. Chem. 46, 4252 (2011).
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 4252
-
-
El Kazzouli, S.1
Du Bellay, A.G.2
Berteina-Raboin, S.3
Delagrange, P.4
Caignard, D.H.5
Guillaumet, G.6
-
88
-
-
20144377689
-
Novel atypical antipsychotic agents: Rational design, an efficient palladium-catalyzed route, and pharmacological studies
-
G. Campiani, S. Butini, C. Fattorusso, F. Trotta, S. Gemma, B. Catalanotti, V. Nacci, I. Fiorini, A. Cagnotto, I. Mereghetti, T. Mennini, P. Minetti, M. A. Di Cesare, M. A. Stasi, S. Di Serio, O. Ghirardi, O. Tinti, and P. Carminati, Novel atypical antipsychotic agents: Rational design, an efficient palladium-catalyzed route, and pharmacological studies. J. Med. Chem. 48, 1705 (2005).
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1705
-
-
Campiani, G.1
Butini, S.2
Fattorusso, C.3
Trotta, F.4
Gemma, S.5
Catalanotti, B.6
Nacci, V.7
Fiorini, I.8
Cagnotto, A.9
Mereghetti, I.10
Mennini, T.11
Minetti, P.12
Di Cesare, M.A.13
Stasi, M.A.14
Di Serio, S.15
Ghirardi, O.16
Tinti, O.17
Carminati, P.18
-
89
-
-
0142133661
-
Synthesis and antiviral activity of novel erythrofuranosyl imidazo[1,2-A]pyridine C-nucleosides constructed via palladium coupling of iodoimidazo[12-A]pyridines and dihydrofuran
-
K. S. Gudmundsson, J. D. Williams, J. C. Drach, and L. B. Townsend, Synthesis and antiviral activity of novel erythrofuranosyl imidazo[1,2-A] pyridine C-nucleosides constructed via palladium coupling of iodoimidazo[1,2-A]pyridines and dihydrofuran. J. Med. Chem. 46, 1449 (2003).
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1449
-
-
Gudmundsson, K.S.1
Williams, J.D.2
Drach, J.C.3
Townsend, L.B.4
-
90
-
-
80051736898
-
N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: A perfect union
-
G. C. Fortman and S. P. Nolan, N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: a perfect union. Chem. Soc. Rev. 40, 5151 (2011).
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 5151
-
-
Fortman, G.C.1
Nolan, S.P.2
-
91
-
-
84871993508
-
Homogeneous palladium-catalyzed asymmetric hydrogenation
-
Q.-A. Chen, Z.-S. Ye, Y. Duan, and Y.-G. Zhou, Homogeneous palladium-catalyzed asymmetric hydrogenation. Chem. Soc. Rev. 42, 497 (2013).
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 497
-
-
Chen, Q.-A.1
Ye, Z.-S.2
Duan, Y.3
Zhou, Y.-G.4
-
92
-
-
65949122326
-
Application of the solvent water in twophase telomerisation reactions and recycling of the homogeneous palladium catalysts
-
A. Behr and J. Leschinski, Application of the solvent water in twophase telomerisation reactions and recycling of the homogeneous palladium catalysts. Green Chem. 11, 609 (2009).
-
(2009)
Green Chem.
, vol.11
, pp. 609
-
-
Behr, A.1
Leschinski, J.2
-
93
-
-
50549097684
-
-
A. Takacs, P. Acs, R. Farkas, G. Kokotos, and L. Kollar. Tetrahedron 64, 9874 (2008).
-
(2008)
Tetrahedron
, vol.64
, pp. 9874
-
-
Takacs, A.1
Acs, P.2
Farkas, R.3
Kokotos, G.4
Kollar, L.5
-
94
-
-
33846893890
-
Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts
-
L. Yin and J. Liebscher, Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 107, 133 (2007).
-
(2007)
Chem. Rev.
, vol.107
, pp. 133
-
-
Yin, L.1
Liebscher, J.2
-
95
-
-
77954063984
-
Engineering metal organic frameworks for heterogeneous catalysis
-
A. Corma, H. Garcia, and F. X. Llabrés i Xamena, Engineering metal organic frameworks for heterogeneous catalysis. Chem. Rev. 110, 4606 (2010).
-
(2010)
Chem. Rev.
, vol.110
, pp. 4606
-
-
Corma, A.1
Garcia, H.2
Llabrés I Xamena, F.X.3
-
96
-
-
84877043533
-
Palladium nanoparticles supported on polymer: An efficient and reusable heterogeneous catalyst for the Suzuki cross-coupling reactions and aerobic oxidation of alcohols
-
K. Karami, M. Ghasemi, and N. H. Naeini, Palladium nanoparticles supported on polymer: An efficient and reusable heterogeneous catalyst for the Suzuki cross-coupling reactions and aerobic oxidation of alcohols. Catal. Comm. 38, 10 (2013).
-
(2013)
Catal. Comm.
, vol.38
, pp. 10
-
-
Karami, K.1
Ghasemi, M.2
Naeini, N.H.3
-
97
-
-
84879182649
-
Palladium nanoparticles supported on zif-8 as an efficient heterogeneous catalyst for aminocarbonylation
-
T. T. Dang, Y. H. Zhu, J. S. Y. Ngiam, S. C. Ghosh, A. Q. Chen, and A. M. Seayad, Palladium nanoparticles supported on ZIF-8 as an efficient heterogeneous catalyst for aminocarbonylation. ASC Catal. 3, 1406 (2013).
-
(2013)
ASC Catal.
, vol.3
, pp. 1406
-
-
Dang, T.T.1
Zhu, Y.H.2
Ngiam, J.S.Y.3
Ghosh, S.C.4
Chen, A.Q.5
Seayad, A.M.6
-
98
-
-
33947727055
-
The sonogashira reaction: A booming methodology in synthetic organic chemistry
-
R. Chinchilla and C. Nájera, The sonogashira reaction: A booming methodology in synthetic organic chemistry. Chem. Rev. 107, 922 (2007).
-
(2007)
Chem. Rev.
, vol.107
, pp. 922
-
-
Chinchilla, R.1
Nájera, C.2
-
99
-
-
80053319803
-
Copper-free Sonogashira cross-coupling for functionalization of alkyne-encoded proteins in aqueous medium and in bacterial cells
-
N. Li, R. K. V. Lim, S. Edwardraja, and Q. Lin, Copper-free Sonogashira cross-coupling for functionalization of alkyne-encoded proteins in aqueous medium and in bacterial cells. J. Am. Chem. Soc. 133, 15316 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 15316
-
-
Li, N.1
Lim, R.K.V.2
Edwardraja, S.3
Lin, Q.4
-
100
-
-
84877123349
-
One-pot and regiospecific synthesis of 2,3-disubstituted indoles from 2-bromoanilides via consecutive palladium-catalyzed Sonogashira coupling, amidopalladation, and reductive elimination
-
B. Z. Lu, H. X. Wei, Y. D. Zhang, W. Y. Zhao, M. Dufour, G. S. Li, V. Farina, and C. H. Senanayake, One-pot and regiospecific synthesis of 2,3-disubstituted indoles from 2-bromoanilides via consecutive palladium-catalyzed Sonogashira coupling, amidopalladation, and reductive elimination. J. Org. Chem. 78, 4558 (2013).
-
(2013)
J. Org. Chem.
, vol.78
, pp. 4558
-
-
Lu, B.Z.1
Wei, H.X.2
Zhang, Y.D.3
Zhao, W.Y.4
Dufour, M.5
Li, G.S.6
Farina, V.7
Senanayake, C.H.8
-
101
-
-
0034249671
-
The heck reaction as a sharpening stone of palladium catalysis
-
I. P. Beletskaya and A. V. Cheprakov, The heck reaction as a sharpening stone of palladium catalysis. Chem. Rev. 100, 3009 (2000).
-
(2000)
Chem. Rev.
, vol.100
, pp. 3009
-
-
Beletskaya, I.P.1
Cheprakov, A.V.2
-
102
-
-
0042379984
-
The asymmetric intramolecular Heck reaction in natural product total synthesis
-
A. B. Dounay and L. E. Overman, The asymmetric intramolecular Heck reaction in natural product total synthesis. Chem. Rev. 103, 2945 (2003).
-
(2003)
Chem. Rev.
, vol.103
, pp. 2945
-
-
Dounay, A.B.1
Overman, L.E.2
-
103
-
-
84880526269
-
Solar energy assisted starchstabilized palladium nanoparticles and their application in C-C coupling reactions
-
A. B. Patil and B. M. Bhanage, Solar energy assisted starchstabilized palladium nanoparticles and their application in C-C coupling reactions. J. Nanosci. Nanotechnol. 13, 5061 (2013).
-
(2013)
J. Nanosci. Nanotechnol.
, vol.13
, pp. 5061
-
-
Patil, A.B.1
Bhanage, B.M.2
-
104
-
-
79952677383
-
Intermolecular dehydrogenative Heck reactions
-
J. Le Bras and J. Muzart, Intermolecular dehydrogenative Heck reactions. Chem. Rev. 111, 1170 (2011).
-
(2011)
Chem. Rev.
, vol.111
, pp. 1170
-
-
Le Bras, J.1
Muzart, J.2
-
105
-
-
79952657415
-
Stille polycondensation for synthesis of functional materials
-
B. Carsten, F. He, H. J. Son, T. Xu, and L. Yu, Stille polycondensation for synthesis of functional materials. Chem. Rev. 111, 1493 (2011).
-
(2011)
Chem. Rev.
, vol.111
, pp. 1493
-
-
Carsten, B.1
He, F.2
Son, H.J.3
Xu, T.4
Yu, L.5
-
106
-
-
80054730816
-
Palladium nanoparticles immobilized on chemically modified silica gel: Efficient heterogeneous catalyst for Suzuki, Stille and Sonogashira cross-coupling reactions
-
P. Dutta and A. Sarkar, Palladium nanoparticles immobilized on chemically modified silica gel: Efficient heterogeneous catalyst for Suzuki, Stille and Sonogashira cross-coupling reactions. Adv. Synth. Catal. 353, 2814 (2011).
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 2814
-
-
Dutta, P.1
Sarkar, A.2
-
107
-
-
80051748635
-
Palladium-catalyzed alkynylation of secondary α-bromo carbonyl compounds via Stille coupling
-
J. Y. Kang and B. T. Connell, Palladium-catalyzed alkynylation of secondary α-bromo carbonyl compounds via Stille coupling. J. Org. Chem. 76, 6856 (2011).
-
(2011)
J. Org. Chem.
, vol.76
, pp. 6856
-
-
Kang, J.Y.1
Connell, B.T.2
-
108
-
-
57549099215
-
Palladium-catalyzed Suzuki- Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands
-
R. Martin and S. L. Buchwald, Palladium-catalyzed Suzuki- Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. Acc. Chem. Res. 41, 1461 (2008).
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 1461
-
-
Martin, R.1
Buchwald, S.L.2
-
109
-
-
34848907405
-
Synthesis of polysubstituted imidazo [1,2- a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation
-
J. Koubachi, S. El Kazzouli, S. Berteina-Raboin, A. Mouaddib, and G. Guillaumet, Synthesis of polysubstituted imidazo[1,2- a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation. J. Org. Chem. 72, 7650 (2007).
-
(2007)
J. Org. Chem.
, vol.72
, pp. 7650
-
-
Koubachi, J.1
El Kazzouli, S.2
Berteina-Raboin, S.3
Mouaddib, A.4
Guillaumet, G.5
-
110
-
-
23244451883
-
Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions
-
S. El Kazzouli, L. Bouissane, M. Khouili, and G. Guillaumet, Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions. Tetrahedron Lett. 46, 6163 (2005).
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 6163
-
-
El Kazzouli, S.1
Bouissane, L.2
Khouili, M.3
Guillaumet, G.4
-
111
-
-
84879196068
-
Microwave-assisted Suzuki- Miyaura cross-coupling of free (NH) 3-bromoindazoles
-
A. Benyahia, M. Naas, N. El Brahmi, S. El Kazzouli, E. M. Essassi, J.-P. Majoral, and G. Guillaumet, Microwave-assisted Suzuki- Miyaura cross-coupling of free (NH) 3-bromoindazoles. Curr. Org. Chem. 17, 304 (2013).
-
(2013)
Curr. Org. Chem.
, vol.17
, pp. 304
-
-
Benyahia, A.1
Naas, M.2
El Brahmi, N.3
El Kazzouli, S.4
Essassi, E.M.5
Majoral, J.-P.6
Guillaumet, G.7
-
112
-
-
84863011479
-
Microwave-assisted facile synthesis of palladium nanoparticles in HEPES solution and their size-dependent catalytic activities to Suzuki reaction
-
W. Zhang, Q. Wang, F. Qin, H. M. Zhou, Z. Lu, and R. Chen, Microwave-assisted facile synthesis of palladium nanoparticles in HEPES solution and their size-dependent catalytic activities to Suzuki reaction. J. Nanosci. Nanotechnol. 11, 7794 (2011).
-
(2011)
J. Nanosci. Nanotechnol.
, vol.11
, pp. 7794
-
-
Zhang, W.1
Wang, Q.2
Qin, F.3
Zhou, H.M.4
Lu, Z.5
Chen, R.6
-
113
-
-
69249123855
-
Nickel-catalysed Negishi cross-coupling reactions: Scope and mechanisms
-
V. B. Phapale and D. J. Cardenas, Nickel-catalysed Negishi cross-coupling reactions: Scope and mechanisms. Chem. Soc. Rev. 38, 1598 (2009).
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 1598
-
-
Phapale, V.B.1
Cardenas, D.J.2
-
114
-
-
77955394207
-
Pd- PEPPSI complexes and the Negishi reaction
-
C. Valente, M. E. Belowich, N. Hadei, and M. G. Organ, Pd- PEPPSI complexes and the Negishi reaction. Eur. J. Org. Chem. 23, 4343 (2010).
-
(2010)
Eur. J. Org. Chem.
, vol.23
, pp. 4343
-
-
Valente, C.1
Belowich, M.E.2
Hadei, N.3
Organ, M.G.4
-
115
-
-
34547943706
-
Investigations on the suzuki-miyaura and negishi couplings with alkenyl phosphates: Application to the synthesis of 1,1-disubstituted alkenes
-
A. L. Hansen, J. P. Ebran, T. M. Gogsig, and T. Skrydstrup, Investigations on the Suzuki-Miyaura and Negishi couplings with alkenyl phosphates: Application to the synthesis of 1,1-disubstituted alkenes. J. Org. Chem. 72, 6464 (2007).
-
(2007)
J. Org. Chem.
, vol.72
, pp. 6464
-
-
Hansen, A.L.1
Ebran, J.P.2
Gogsig, T.M.3
Skrydstrup, T.4
-
116
-
-
76249124052
-
Clean synthesis of triarylamines: Buchwald-Hartwig reaction in water with amphiphilic resinsupported palladium complexes
-
Y. Hirai and Y. Uozumi, Clean synthesis of triarylamines: Buchwald-Hartwig reaction in water with amphiphilic resinsupported palladium complexes. Chem. Comm. 46, 1103 (2010).
-
(2010)
Chem. Comm.
, vol.46
, pp. 1103
-
-
Hirai, Y.1
Uozumi, Y.2
-
117
-
-
84859970121
-
Ligand-free Buchwald-Hartwig aromatic aminations of aryl halides catalyzed by low-leaching and highly recyclable sulfur-modified gold-supported palladium
-
M. Al-Amin, T. Honma, N. Hoshiya, S. Shuto, and M. Arisawa, Ligand-free Buchwald-Hartwig aromatic aminations of aryl halides catalyzed by low-leaching and highly recyclable sulfur-modified gold-supported palladium. Adv. Synth. Catal. 354, 1061 (2012).
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 1061
-
-
Al-Amin, M.1
Honma, T.2
Hoshiya, N.3
Shuto, S.4
Arisawa, M.5
-
118
-
-
84866364612
-
Domino aziridine ring opening and Buchwald-Hartwig type coupling-cyclization by palladium catalyst
-
R. K. Rao, I. Karthikeyan, and G. Sekar, Domino aziridine ring opening and Buchwald-Hartwig type coupling-cyclization by palladium catalyst. Tetrahedron 68, 9090 (2012).
-
(2012)
Tetrahedron
, vol.68
, pp. 9090
-
-
Rao, R.K.1
Karthikeyan, I.2
Sekar, G.3
-
119
-
-
33845602612
-
Regioselective palladium-catalyzed arylation and heteroarylation of imidazo [1,2-A]pyridines
-
J. Koubachi, S. El Kazzouli, S. Berteina-Raboin, A. Mouaddib, and G. Guillaumet, Regioselective palladium-catalyzed arylation and heteroarylation of imidazo[1,2-A]pyridines. Synlett 3237 (2006).
-
(2006)
Synlett
, vol.3237
-
-
Koubachi, J.1
El Kazzouli, S.2
Berteina-Raboin, S.3
Mouaddib, A.4
Guillaumet, G.5
-
120
-
-
84869124383
-
Efficient synthesis and first regioselective C-3 direct arylation of imidazo [1,2-b]pyrazoles
-
S. Grosse, C. Pillard, S. Massip, J. M. Leger, C. Jarry, S. Bourg, P. Bernard, and G. Guillaumet, Efficient synthesis and first regioselective C-3 direct arylation of imidazo[1,2-b]pyrazoles. Chem. Eur. J. 18, 14943 (2012).
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 14943
-
-
Grosse, S.1
Pillard, C.2
Massip, S.3
Leger, J.M.4
Jarry, C.5
Bourg, S.6
Bernard, P.7
Guillaumet, G.8
-
121
-
-
74849140182
-
Metal-catalyzed alphaarylation of carbonyl and related molecules: Novel trends in C C bond formation by C H bond functionalization
-
C. C. C. Johansson and T. J. Colacot, Metal-catalyzed alphaarylation of carbonyl and related molecules: Novel trends in C C bond formation by C H bond functionalization. Angw. Chem. Int. Ed. 49, 676 (2010).
-
(2010)
Angw. Chem. Int. Ed.
, vol.49
, pp. 676
-
-
Johansson, C.C.C.1
Colacot, T.J.2
-
122
-
-
80054972215
-
Transition metal-catalyzed arylation of unactivated C(sp(3)) H bonds
-
O. Baudoin, Transition metal-catalyzed arylation of unactivated C(sp(3)) H bonds. Chem. Soc. Rev. 40, 4902 (2011).
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4902
-
-
Baudoin, O.1
-
123
-
-
84870601851
-
Direct C-3-arylations of 1H-indazoles
-
A. Benyahia, M. Naas, S. El Kazzouli, E. M. Essassi, and G. Guillaumet, Direct C-3-arylations of 1H-indazoles. Eur. J. Org. Chem. 36, 7075 (2012).
-
(2012)
Eur. J. Org. Chem.
, vol.36
, pp. 7075
-
-
Benyahia, A.1
Naas, M.2
El Kazzouli, S.3
Essassi, E.M.4
Guillaumet, G.5
-
124
-
-
78649612564
-
Transition-metalcatalyzed direct C-H alkenylation, alkynylation, benzylation, and alkylation of (hetero)arenes
-
S. Messaoudi, J. D. Brion, and M. Alami, Transition-metalcatalyzed direct C-H alkenylation, alkynylation, benzylation, and alkylation of (hetero)arenes. Eur. J. Org. Chem. 34, 6495 (2010).
-
(2010)
Eur. J. Org. Chem.
, vol.34
, pp. 6495
-
-
Messaoudi, S.1
Brion, J.D.2
Alami, M.3
-
125
-
-
84869403542
-
Free-amine-directed alkenylation of C(sp(2))-H and cycloamination by palladium catalysis
-
Z. J. Liang, L. Ju, Y. J. Xie, L. H. Huang, and Y. H. Zhang, Free-amine-directed alkenylation of C(sp(2))-H and cycloamination by palladium catalysis. Chem. Eur. J. 49, 15816 (2012).
-
(2012)
Chem. Eur. J.
, vol.49
, pp. 15816
-
-
Liang, Z.J.1
Ju, L.2
Xie, Y.J.3
Huang, L.H.4
Zhang, Y.H.5
-
126
-
-
50849118498
-
New and efficient palladium (0)-mediated microwave-assisted direct c3 alkenylation of imidazo[1,2-A]pyridines
-
J. Koubachi, S. El Kazzouli, S. Berteina-Raboin, A. Mouaddib, and G. Guillaumet, New and efficient palladium(0)-mediated microwave-assisted direct C3 alkenylation of imidazo[1,2- a]pyridines. Synthesis 2537 (2008).
-
(2008)
Synthesis
, vol.2537
-
-
Koubachi, J.1
El Kazzouli, S.2
Berteina-Raboin, S.3
Mouaddib, A.4
Guillaumet, G.5
-
127
-
-
84874025350
-
C2-selective direct alkynylation of indoles
-
G. L. Tolnai, S. Ganss, J. P. Brand, and J. Waser, C2-selective direct alkynylation of indoles. Org. Lett. 15, 112 (2013).
-
(2013)
Org. Lett.
, vol.15
, pp. 112
-
-
Tolnai, G.L.1
Ganss, S.2
Brand, J.P.3
Waser, J.4
-
128
-
-
84862572654
-
Palladium-catalyzed C H bond direct alkynylation of 5-membered heteroarenes: A well-defined synthetic route to azole derivatives containing two different alkynyl groups
-
F. Shibahara, Y. Dohke, and T. J. Murai, Palladium-catalyzed C H bond direct alkynylation of 5-membered heteroarenes: A well-defined synthetic route to azole derivatives containing two different alkynyl groups. J. Org. Chem. 77, 5381 (2013).
-
(2013)
J. Org. Chem.
, vol.77
, pp. 5381
-
-
Shibahara, F.1
Dohke, Y.2
Murai, T.J.3
-
129
-
-
0242694953
-
Palladium-containing perovskites: Recoverable and reuseable catalysts for Suzuki couplings
-
M. D. Smith, A. F. Stepan, C. Ramarao, P. E. Brennan, and S. V. Ley, Palladium-containing perovskites: Recoverable and reuseable catalysts for Suzuki couplings. Chem. Comm. 2652 (2003).
-
(2003)
Chem. Comm.
, vol.2652
-
-
Smith, M.D.1
Stepan, A.F.2
Ramarao, C.3
Brennan, P.E.4
Ley, S.V.5
-
130
-
-
18244366860
-
Heterogeneous or homogeneous? A case study involving palladiumcontaining perovskites in the Suzuki reaction
-
S. P. Andrews, A. F. Stepan, H. Tanaka, S. V. Ley, and M. D. Smith, Heterogeneous or homogeneous? A case study involving palladiumcontaining perovskites in the Suzuki reaction. Adv. Synth. Catal. 347, 647 (2005).
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 647
-
-
Andrews, S.P.1
Stepan, A.F.2
Tanaka, H.3
Ley, S.V.4
Smith, M.D.5
-
131
-
-
35348969025
-
Palladium-doped mixed oxides as 'slow-release' catalysts for Suzuki couplings
-
U. Kazmaier, S. Hähn, T. D. Weiss, R. Kautenburger, and W. F. Maier, Palladium-doped mixed oxides as 'slow-release' catalysts for Suzuki couplings. Synlett. 16, 2579 (2007).
-
(2007)
Synlett.
, vol.16
, pp. 2579
-
-
Kazmaier, U.1
Hähn, S.2
Weiss, T.D.3
Kautenburger, R.4
Maier, W.F.5
-
132
-
-
84878638599
-
Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: A remarkable advance from palladium to nickel catalysts
-
F.-S. Han, Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: a remarkable advance from palladium to nickel catalysts. Chem. Soc. Rev. 42, 5270 (2013).
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 5270
-
-
Han, F.-S.1
-
133
-
-
84872563127
-
Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations
-
S. L. Zultanski and G. C. Fu, Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations. J. Am. Chem. Soc. 135, 624 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 624
-
-
Zultanski, S.L.1
Fu, G.C.2
-
134
-
-
84865643904
-
Multifunctional mesoporous silica supported palladium nanoparticles as efficient and reusable catalyst for water-medium Ullmann reaction
-
J. L. Huang, J. W. Yin, W. Chai, C. Liang, J. Shen, and F. Zhang, Multifunctional mesoporous silica supported palladium nanoparticles as efficient and reusable catalyst for water-medium Ullmann reaction. New J. Chem. 36, 1378 (2012).
-
(2012)
New J. Chem.
, vol.36
, pp. 1378
-
-
Huang, J.L.1
Yin, J.W.2
Chai, W.3
Liang, C.4
Shen, J.5
Zhang, F.6
-
135
-
-
79951933560
-
New role of graphene oxide as active hydrogen donor in the recyclable palladium nanoparticles catalyzed ullmann reaction in environmental friendly ionic liquid/supercritical carbon dioxide system
-
J. S. Cheng, G. C. Zhang, J. H. Du, L. Y. Tang, J. Y. Xu, and J. H. Li, New role of graphene oxide as active hydrogen donor in the recyclable palladium nanoparticles catalyzed ullmann reaction in environmental friendly ionic liquid/supercritical carbon dioxide system. J. Mat. Chem. 21, 3485 (2011).
-
(2011)
J. Mat. Chem.
, vol.21
, pp. 3485
-
-
Cheng, J.S.1
Zhang, G.C.2
Du, J.H.3
Tang, L.Y.4
Xu, J.Y.5
Li, J.H.6
-
136
-
-
19944369406
-
Copper- and palladiumcontaining perovskites: Catalysts for the ullmann and sonogashira reactions
-
S. Lohmann, S. P. Andrews, B. J. Burke, M. D. Smith, J. P. Attfield, H. Tanaka, K. Kaneko, and S. V. Ley, Copper- and palladiumcontaining perovskites: Catalysts for the Ullmann and Sonogashira reactions. Synlett. 8, 1291 (2005).
-
(2005)
Synlett.
, vol.8
, pp. 1291
-
-
Lohmann, S.1
Andrews, S.P.2
Burke, B.J.3
Smith, M.D.4
Attfield, J.P.5
Tanaka, H.6
Kaneko, K.7
Ley, S.V.8
-
137
-
-
0242459935
-
First examples of transition-metal free Sonogashira-type couplings
-
N. E. Leadbeater, M. Marco, and B. J. Tominack, First examples of transition-metal free Sonogashira-type couplings. Org. Lett. 5, 3919 (2003).
-
(2003)
Org. Lett.
, vol.5
, pp. 3919
-
-
Leadbeater, N.E.1
Marco, M.2
Tominack, B.J.3
-
138
-
-
2342583283
-
Palladium-free and ligand-free Sonogashira cross-coupling
-
M. B. Thathagar, J. Beckers, and G. Rothenberg, Palladium-free and ligand-free Sonogashira cross-coupling. Green Chem. 6, 215 (2004).
-
(2004)
Green Chem.
, vol.6
, pp. 215
-
-
Thathagar, M.B.1
Beckers, J.2
Rothenberg, G.3
-
139
-
-
0347992908
-
Transitionmetal- free Sonogashira-type coupling reactions in water
-
P. Appukkuttan, W. Dehaen, and E. Van der Eycken, Transitionmetal- free Sonogashira-type coupling reactions in water. Eur. J. Org. Chem. 4713 (2003).
-
(2003)
Eur. J. Org. Chem.
, vol.4713
-
-
Appukkuttan, P.1
Dehaen, W.2
Eycken Der E.Van3
-
140
-
-
80054995660
-
35 years of palladium-catalyzed cross-coupling with Grignard reagents: How far have we come?
-
C. E. I. Knappke and A. J. von Wangelin, and J. von Wangelin, 35 years of palladium-catalyzed cross-coupling with Grignard reagents: how far have we come? Chem. Soc. Rev. 40, 4948 (2011).
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4948
-
-
Knappke, C.E.I.1
Von Wangelin, A.J.2
Von Wangelin, J.3
-
141
-
-
84870879744
-
Palladiumcatalyzed Kumada coupling reaction of bromoporphyrins with silylmethyl Grignard reagents: Preparation of silylmethyl-substituted porphyrins as a multipurpose synthon for fabrication of porphyrin systems
-
N. Sugita, S. Hayashi, F. Hino, and T. Takanami, Palladiumcatalyzed Kumada coupling reaction of bromoporphyrins with silylmethyl Grignard reagents: Preparation of silylmethyl-substituted porphyrins as a multipurpose synthon for fabrication of porphyrin systems. J. Org. Chem. 77, 10488 (2012).
-
(2012)
J. Org. Chem.
, vol.77
, pp. 10488
-
-
Sugita, N.1
Hayashi, S.2
Hino, F.3
Takanami, T.4
-
142
-
-
74849133511
-
DHTP Ligands for the highly ortho-selective, palladium-catalyzed cross-coupling of dihaloarenes with Grignard reagents: A Conformational Approach for Catalyst Improvement
-
S. Ishikawa and K. Manabe, DHTP Ligands for the highly ortho-selective, palladium-catalyzed cross-coupling of dihaloarenes with Grignard reagents: A Conformational Approach for Catalyst Improvement. Angew. Chem. Int. Ed. 49, 779 (2010).
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 779
-
-
Ishikawa, S.1
Manabe, K.2
-
143
-
-
78651386712
-
Cross-coupling of Grignard reagents with alkyl halides or tosylates by the use of nickel or palladium containing perovskite
-
S. P. Singh, T. Iwasaki, J. Terao, and N. Kambe, Cross-coupling of Grignard reagents with alkyl halides or tosylates by the use of nickel or palladium containing perovskite. Tetrahedron Lett. 52, 774 (2011).
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 774
-
-
Singh, S.P.1
Iwasaki, T.2
Terao, J.3
Kambe, N.4
|