-
1
-
-
56649117022
-
Ligandless Heck coupling between a halogenated aniline and acrylonitrile catalyzed by Pd/C: Development and optimization of an industrial-scale Heck process for the production of a pharmaceutical intermediate
-
Schils, D.; Stappers, F.; Solberghe, G.; van Heck, R.; Coppens, M.; Van den Heuvel, D.; Van der Donck, P.; Callewaert, T.; Meeussen, F.; De Bie, E.; Eersels, K.; Schouteden, E. Ligandless Heck coupling between a halogenated aniline and acrylonitrile catalyzed by Pd/C: Development and optimization of an industrial-scale Heck process for the production of a pharmaceutical intermediate. Org. Process Res. Dev. 2008, 12, 530-536.
-
(2008)
Org. Process Res. Dev
, vol.12
, pp. 530-536
-
-
Schils, D.1
Stappers, F.2
Solberghe, G.3
van Heck, R.4
Coppens, M.5
van den Heuvel, D.6
van der Donck, P.7
Callewaert, T.8
Meeussen, F.9
de Bie, E.10
Eersels, K.11
Schouteden, E.12
-
2
-
-
0035839707
-
Supported palladium catalysts for fine chemicals synthesis
-
Blaser, H.-U.; Indolese, A.; Schnyder, A.; Steiner, H.; Studer, M. Supported palladium catalysts for fine chemicals synthesis. J. Mol. Catal. A Chem. 2001, 173, 3-18.
-
(2001)
J. Mol. Catal. a Chem
, vol.173
, pp. 3-18
-
-
Blaser, H.-U.1
Indolese, A.2
Schnyder, A.3
Steiner, H.4
Studer, M.5
-
4
-
-
33745657681
-
For the Suzuki-Miyaura reaction
-
For the Suzuki-Miyaura reaction. Eur. J. Org. Chem. 2006, 2679-2690.
-
(2006)
Eur. J. Org. Chem
, pp. 2679-2690
-
-
-
5
-
-
33749515284
-
Recent advances in Pd/C-catalyzed coupling reactions
-
Seki, M. Recent advances in Pd/C-catalyzed coupling reactions. Synthesis 2006, 2975-2992.
-
(2006)
Synthesis
, pp. 2975-2992
-
-
Seki, M.1
-
6
-
-
33846893890
-
Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts
-
Yin, L.; Liebscher, J. Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 2007, 107, 133-173.
-
(2007)
Chem. Rev
, vol.107
, pp. 133-173
-
-
Yin, L.1
Liebscher, J.2
-
7
-
-
72049112575
-
Palladium-catalyzed alkynylation of aryl and hetaryl halides: A journey from conventional palladium complexes or salts for palladium/carbon
-
Pal, M. Palladium-catalyzed alkynylation of aryl and hetaryl halides: A journey from conventional palladium complexes or salts for palladium/carbon. Synlett 2009, 2896-2912.
-
(2009)
Synlett
, pp. 2896-2912
-
-
Pal, M.1
-
8
-
-
70349226817
-
Silica-supported palladium: Sustainable catalysts for cross-coupling reactions
-
Polshettiwar, V.; Len, C.; Fihri, A. Silica-supported palladium: Sustainable catalysts for cross-coupling reactions. Coord. Chem. Rev. 2009, 253, 2599-2626.
-
(2009)
Coord. Chem. Rev
, vol.253
, pp. 2599-2626
-
-
Polshettiwar, V.1
Len, C.2
Fihri, A.3
-
10
-
-
0032512085
-
A novel type of PdM/C-catalyzed hydrogenation using a catalyst poison: Chemoselective inhibition of the hydrogenolysis for O-benzyl protective group by the addition of a nitrogen-containing base
-
Sajiki, H.; Hirota, K. A novel type of PdM/C-catalyzed hydrogenation using a catalyst poison: Chemoselective inhibition of the hydrogenolysis for O-benzyl protective group by the addition of a nitrogen-containing base. Tetrahedron 1998, 54, 13981-13996.
-
(1998)
Tetrahedron
, vol.54
, pp. 13981-13996
-
-
Sajiki, H.1
Hirota, K.2
-
11
-
-
33746901223
-
Pd/C-catalyzed chemoselective hydrogenation in the presence of diphenyl-sulfide
-
Mori, A.; Miyakawa, Y.; Ohashi, E.; Haga, T.; Maegawa, T.; Sajiki, H. Pd/C-catalyzed chemo selective hydrogenation in the presence of diphenyl-sulfide. Org. Lett. 2006, 8, 3279-3281.
-
(2006)
Org. Lett
, vol.8
, pp. 3279-3281
-
-
Mori, A.1
Miyakawa, Y.2
Ohashi, E.3
Haga, T.4
Maegawa, T.5
Sajiki, H.6
-
12
-
-
0037201097
-
Mild and general procedure for Pd/C-catalyzed hydrodechlorination of aromatic chlorides
-
Sajiki, H.; Kume, A.; Hattori, K.; Hirota, K. Mild and general procedure for Pd/C-catalyzed hydrodechlorination of aromatic chlorides. Tetrahedron Lett 2002, 43, 7247-7250.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 7247-7250
-
-
Sajiki, H.1
Kume, A.2
Hattori, K.3
Hirota, K.4
-
13
-
-
0037201150
-
3N system under ambient pressure and temperature
-
Sajiki, H.; Kume, A.; Hattori, K.; Nagase, H.; Hirota, K. Complete and truly catalytic degradation method of PCBs using Pd/C-Et3N system under ambient pressure and temperature. Tetrahedron Lett. 2002, 43, 7251-7254.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 7251-7254
-
-
Sajiki, H.1
Kume, A.2
Hattori, K.3
Nagase, H.4
Hirota, K.5
-
14
-
-
33745631204
-
3N-mediated catalytic hydrodechlorination of aromatic chlorides under mild conditions
-
Monguchi, Y.; Kume, A.; Hattori, K.; Maegawa, T.; Sajiki, H. Pd/C-Et3N-mediated catalytic hydrodechlorination of aromatic chlorides under mild conditions. Tetrahedron 2006, 62, 7926-7933.
-
(2006)
Tetrahedron
, vol.62
, pp. 7926-7933
-
-
Monguchi, Y.1
Kume, A.2
Hattori, K.3
Maegawa, T.4
Sajiki, H.5
-
15
-
-
33746115680
-
3N system under ambient pressure and temperature
-
Monguchi, Y.; Kume, A.; Sajiki, H. Facile and catalytic degradation method of DDT using Pd/C-Et3N system under ambient pressure and temperature. Tetrahedron 2006, 62, 8384-8392.
-
(2006)
Tetrahedron
, vol.62
, pp. 8384-8392
-
-
Monguchi, Y.1
Kume, A.2
Sajiki, H.3
-
16
-
-
44649099034
-
Pd/C-catalyzed practical degradation of PCBs at room temperature
-
Kume, A.; Monguchi, Y.; Hattori, K.; Nagase, H. Sajiki, H. Pd/C-catalyzed practical degradation of PCBs at room temperature. Appl. Catal B Environ. 2008, 81, 274-282.
-
(2008)
Appl. Catal B Environ
, vol.81
, pp. 274-282
-
-
Kume, A.1
Monguchi, Y.2
Hattori, K.3
Nagase, H.4
Sajiki, H.5
-
17
-
-
61849107320
-
Temperature-dependent suppression of palladium on carbon-catalyzed hy-drogenations
-
Bora, U.; Yaguchi, K.; Kume, A.; Maegawa, T.; Monguchi, Y.; Sajiki, H. Temperature-dependent suppression of palladium on carbon-catalyzed hy-drogenations. Catal. Commun. 2009, 10, 1161-1165.
-
(2009)
Catal. Commun
, vol.10
, pp. 1161-1165
-
-
Bora, U.1
Yaguchi, K.2
Kume, A.3
Maegawa, T.4
Monguchi, Y.5
Sajiki, H.6
-
18
-
-
0037156431
-
Reductive amination of aldehydes and ketones by a Hantzsch dihydropyridine using scandium triflate as a catalyst
-
Itoh, T.; Nagata, K.; Kurihara, A.; Miyazaki, M.; Ohsawa, A. Reductive amination of aldehydes and ketones by a Hantzsch dihydropyridine using scandium triflate as a catalyst. Tetrahedron Lett. 2002, 43, 3105-3108.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 3105-3108
-
-
Itoh, T.1
Nagata, K.2
Kurihara, A.3
Miyazaki, M.4
Ohsawa, A.5
-
19
-
-
10944220196
-
A metal-free transfer hydrogenation: Organocatalytic conjugate reduction of α,β-unsaturated aldehydes
-
Yang, J. W.; Fonseca, M. T. H.; List, B; Yang, J. W.; Fonseca, M. T. H.; Vignola, N; List, B. A metal-free transfer hydrogenation: Organocatalytic conjugate reduction of α,β-unsaturated aldehydes. Angew. Chem. Int. Ed. 2004, 43, 6660-6662.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 6660-6662
-
-
Yang, J.W.1
Fonseca, M.T.H.2
List, B.3
Yang, J.W.4
Fonseca, M.T.H.5
Vignola, N.6
List, B.7
-
20
-
-
11244320360
-
Metal-free, organocatalytic symmetric transfer hydrogenation of α,β-unsaturated aldehydes
-
Yang, J. W.; Fonseca, M. T. H.; Vignola, N; List, B. Metal-free, organocatalytic symmetric transfer hydrogenation of α,β-unsaturated aldehydes. Angew. Chem. Int. Ed. 2005, 44, 108-110.
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 108-110
-
-
Yang, J.W.1
Fonseca, M.T.H.2
Vignola, N.3
List, B.4
-
21
-
-
33746286405
-
Asymmetric counteranion-directed catalysis
-
Mayer, S.; List, B. Asymmetric counteranion-directed catalysis. Angew. Chem. Int. Ed. 2006, 45, 4193-4195.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 4193-4195
-
-
Mayer, S.1
List, B.2
-
22
-
-
55849128876
-
Reduction of N-(alkoxy(aryl)methyl)benzamide compounds by a Hantzsch ester 1,4-dihydropyridine using Pd/C as a catalyst
-
Shen, X.-X.; Liu, Q.; Xing, R.-G.; Zhou, B. Reduction of N-(alkoxy(aryl)methyl)benzamide compounds by a Hantzsch ester 1,4-dihydropyridine using Pd/C as a catalyst. Catal. Lett. 2008, 126, 361-366.
-
(2008)
Catal. Lett
, vol.126
, pp. 361-366
-
-
Shen, X.-X.1
Liu, Q.2
Xing, R.-G.3
Zhou, B.4
-
23
-
-
66349095460
-
Pd/C-catalyzed transfer hydrogenation with Hantzsch ester 1,4-dihydropyridine for the reduction of aromatic azides, aromatic nitro compounds and olefins
-
Niu, X.; Liu, Z.; Yu, W.; Wu, L. Pd/C-catalyzed transfer hydrogenation with Hantzsch ester 1,4-dihydropyridine for the reduction of aromatic azides, aromatic nitro compounds and olefins. Chin. J. Org. Chem. 2009, 29, 229-233.
-
(2009)
Chin. J. Org. Chem
, vol.29
, pp. 229-233
-
-
Niu, X.1
Liu, Z.2
Yu, W.3
Wu, L.4
-
24
-
-
58149494194
-
Hydro-genation of olefins using Hantzsch ester catalyzed by palladium on carbon
-
Liu, Q.; Li, J.; Shen, X.-X.; Xing, R.-G.; Yang, J.; Liu, Z.; Zhou, B. Hydro-genation of olefins using Hantzsch ester catalyzed by palladium on carbon. Tetrahedron Lett. 2009, 50, 1026-1028.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 1026-1028
-
-
Liu, Q.1
Li, J.2
Shen, X.-X.3
Xing, R.-G.4
Yang, J.5
Liu, Z.6
Zhou, B.7
-
25
-
-
0001617511
-
Catalytic hydrogen transfer reductions using ammonium formate
-
Ranu, B. C; Sarkar, A.; Guchhait, S. K.; Ghosh, K. Catalytic hydrogen transfer reductions using ammonium format. A review. J. Ind. Chem. Soc. 1998, 75, 690-694.
-
(1998)
A Review. J. Ind. Chem. Soc
, vol.75
, pp. 690-694
-
-
Ranu, B.C.1
Sarkar, A.2
Guchhait, S.K.3
Ghosh, K.4
-
26
-
-
0037017708
-
A chemoselective method for the reductive N-formylation of aryl azides under catalytic transfer hydrogenation conditions
-
Reddy, P. G.; Baskaran, S. A chemoselective method for the reductive N-formylation of aryl azides under catalytic transfer hydrogenation conditions. Tetrahedron Lett. 2002, 43, 1919-1922.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 1919-1922
-
-
Reddy, P.G.1
Baskaran, S.2
-
27
-
-
61849173411
-
Reactivity versus stability of oxiranes under palladium-catalyzed reductive conditions
-
Thiery, E.; Le Bras, J.; Muzart, J. Reactivity versus stability of oxiranes under palladium-catalyzed reductive conditions. Eur. J. Org. Chem. 2009, 961-985.
-
(2009)
Eur. J. Org. Chem
, pp. 961-985
-
-
Thiery, E.1
Le Bras, J.2
Muzart, J.3
-
28
-
-
40649108258
-
A convenient method for the syn-theses of tetrahydrofuran moiety from furan by catalytic transfer of hydrogenation with ammonium formate
-
Nandy, S. K.; Liu, J.; Padmapriya, A. A. A convenient method for the syn-theses of tetrahydrofuran moiety from furan by catalytic transfer of hydrogenation with ammonium formate. Tetrahedron Lett. 2008, 49, 2469-2471.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 2469-2471
-
-
Nandy, S.K.1
Liu, J.2
Padmapriya, A.A.3
-
29
-
-
34249752590
-
Reductive coupling reactions of 2-nitrochalcones and their p-hydroxy-analogues: New syntheses of 2-arylquinoline and 2-aryl-4-hydroxyquinoline derivatives
-
Barros, A. I. R. N. A.; Dias, A. F. R.; Silva, A. M. S. Reductive coupling reactions of 2-nitrochalcones and their p-hydroxy-analogues: New syntheses of 2-arylquinoline and 2-aryl-4-hydroxyquinoline derivatives. Monatsh. Chem. 2007, 138, 585-594.
-
(2007)
Monatsh. Chem
, vol.138
, pp. 585-594
-
-
Barros A. I. R. N., A.1
Dias, A.F.R.2
Silva, A.M.S.3
-
30
-
-
33749517198
-
Pd-C/ammonium formate: A selective catalyst for the hydrogenation of chalcones to dihydrochalcones
-
Ahmed, N; van Lier, J. E. Pd-C/ammonium formate: A selective catalyst for the hydrogenation of chalcones to dihydrochalcones. J. Chem. Res. Synapses 2006, 584-585.
-
(2006)
J. Chem. Res. Synapses
, pp. 584-585
-
-
Ahmed, N.1
van Lier, J.E.2
-
31
-
-
40949090544
-
Synthesis and pharmacological evaluation of bicyclic SNC80 analogues with separated benzhydryl moiety
-
Jung, B.; Englberger, W.; Fröhlich, R.; Schepmann, D.; Lehmkuhl, K.; Wünsch, B. Synthesis and pharmacological evaluation of bicyclic SNC80 analogues with separated benzhydryl moiety. Bioorg Med. Chem. 2008, 16, 2870-2885.
-
(2008)
Bioorg Med. Chem
, vol.16
, pp. 2870-2885
-
-
Jung, B.1
Englberger, W.2
Fröhlich, R.3
Schepmann, D.4
Lehmkuhl, K.5
Wünsch, B.6
-
32
-
-
34547936934
-
Pd-C-induced catalytic transfer hydrogenation with triethylsilane
-
Mandal, P. K.; McMurray, J. S. Pd-C-induced catalytic transfer hydrogenation with triethylsilane. J. Org. Chem. 2007, 72, 6599-6601.
-
(2007)
J. Org. Chem
, vol.72
, pp. 6599-6601
-
-
Mandal, P.K.1
McMurray, J.S.2
-
33
-
-
3242669637
-
Alternative sources of hydrogen for hydrodechlorination of chlorinated organic compounds in water on Pd catalysts
-
Kopinke, F.-D.; Mackenzie, K.; Koehler, R.; Georgi, A. Alternative sources of hydrogen for hydrodechlorination of chlorinated organic compounds in water on Pd catalysts. App. Catal. A Gen. 2004, 271, 119-128.
-
(2004)
App. Catal. a Gen
, vol.271
, pp. 119-128
-
-
Kopinke, F.-D.1
Mackenzie, K.2
Koehler, R.3
Georgi, A.4
-
34
-
-
28244454816
-
New trends in palladium-catalyzed transfer hydrogenations using formic acid
-
Prasad, K.; Jiang, X.; Slade, J. S.; Clemens, J.; Repic, O.; Black lock, T. J. New trends in palladium-catalyzed transfer hydrogenations using formic acid. Adv. Synth. Catal. 2005, 347, 1769-1773.
-
(2005)
Adv. Synth. Catal
, vol.347
, pp. 1769-1773
-
-
Prasad, K.1
Jiang, X.2
Slade, J.S.3
Clemens, J.4
Repic, O.5
Blacklock, T.J.6
-
35
-
-
77955519761
-
An efficient reduction of quinones by formate-palladium/carbon system
-
Pande, P. P. An efficient reduction of quinones by formate-palladium/carbon system. Asian J. Chem. 2010, 22, 2549-2553.
-
(2010)
Asian J. Chem
, vol.22
, pp. 2549-2553
-
-
Pande, P.P.1
-
36
-
-
24144483443
-
One-pot multi-step synthesis: A challenge spawning innovation
-
For a general review regarding one-pot reactions, see
-
For a general review regarding one-pot reactions, see: Broadwater, S. J.; Roth, S. L.; Price, K. E.; Kobaslija, M.; McQuade, D. T. One-pot multi-step synthesis: A challenge spawning innovation. Org. Biomol. Chem. 2005, 3, 2899-2906.
-
(2005)
Org. Biomol. Chem
, vol.3
, pp. 2899-2906
-
-
-
37
-
-
7044235263
-
Domino reactions in organic synthesis
-
For a general review regarding one-pot reactions, see
-
For a general review regarding one-pot reactions, see: Tietze, L. F. Domino reactions in organic synthesis. Chem. Rev. 1996, 96, 115-136.
-
(1996)
Chem. Rev
, vol.96
, pp. 115-136
-
-
Tietze, L.F.1
-
38
-
-
33750173220
-
Sequential transformations in organic chemistry: A synthetic strategy with a future
-
For a general review regarding one-pot reactions, see
-
For a general review regarding one-pot reactions, see: Tietze, L. F.; Beifuss, U. Sequential transformations in organic chemistry: A synthetic strategy with a future. Angew. Chem. Int. Ed. Engl. 1993, 32, 131-163.
-
(1993)
Angew. Chem. Int. Ed. Engl
, vol.32
, pp. 131-163
-
-
Tietze, L.F.1
Beifuss, U.2
-
40
-
-
0035840229
-
Synthesis of secondary amines
-
Salvatore, R. N.; Yoon, C. H.; Jung, K. W. Synthesis of secondary amines. Tetrahedron 2001, 57, 7785-7811.
-
(2001)
Tetrahedron
, vol.57
, pp. 7785-7811
-
-
Salvatore, R.N.1
Yoon, C.H.2
Jung, K.W.3
-
41
-
-
0034619188
-
14
-
Bae, J. W.; Cho, Y. J.; Lee, S. H.; Yoon, C.-O. M.; Yoon, C. M. A one-pot synthesis of N-alkylaminobenzenes from nitro aromatics: Reduction followed by reductive amination using B10H14. Chem. Commun. 2000, 1857-1858.
-
(2000)
Chem. Commun
, pp. 1857-1858
-
-
Bae, J.W.1
Cho, Y.J.2
Lee, S.H.3
Yoon C.-O., M.4
Yoon, C.M.5
-
42
-
-
0344926568
-
An efficient conversion of nitroaromatics and aromatic amines to tertiary amines in one-pot way
-
see: Jung, Y. J.; Bae, J. W.; Park, E. S.; Chang, Y. M.; Yoon, C. M., later extended the chemistry described in reference 40 to the synthesis of tertiary aromatic amines containing two different alkyl groups, see
-
Yoon et al. later extended the chemistry described in reference 40 to the synthesis of tertiary aromatic amines containing two different alkyl groups, see: Jung, Y. J.; Bae, J. W.; Park, E. S.; Chang, Y. M.; Yoon, C. M. An efficient conversion of nitroaromatics and aromatic amines to tertiary amines in one-pot way. Tetrahedron 2003, 59, 10331-10338.
-
(2003)
Tetrahedron
, vol.59
, pp. 10331-10338
-
-
Yoon1
-
43
-
-
0032010424
-
Selective synthesis of N-monoalkyl aryl-amies from nitro aromatic compounds by reduction-alkylation
-
Xiaojian, Z.; Zuwang, W.; Li, L.; Guijuan, W.; Jiaping, L. Selective synthesis of N-monoalkyl aryl-amies from nitro aromatic compounds by reduction-alkylation. Dyes Pigments 1998, 36, 365-371.
-
(1998)
Dyes Pigments
, vol.36
, pp. 365-371
-
-
Xiaojian, Z.1
Zuwang, W.2
Li, L.3
Guijuan, W.4
Jiaping, L.5
-
44
-
-
12344257727
-
Reductive and catalytic monoalkylation of primary amines using nitriles as an alkylating reagent
-
Sajiki, H.; Ikawa, T.; Hirota, K. Reductive and catalytic monoalkylation of primary amines using nitriles as an alkylating reagent. Org. Lett. 2004, 6, 4977-4980.
-
(2004)
Org. Lett
, vol.6
, pp. 4977-4980
-
-
Sajiki, H.1
Ikawa, T.2
Hirota, K.3
-
46
-
-
13844266938
-
Reductive monoalkylation of aromatic and aliphatic nitro compounds and the corresponding amines with nitriles
-
Nacario, R.; Kotakonda, S.; Fouchard, D. M. D.; Tillekeratne, L. M. V.; Hudson, R. A. Reductive monoalkylation of aromatic and aliphatic nitro compounds and the corresponding amines with nitriles. Org. Lett. 2005, 7, 471-474.
-
(2005)
Org. Lett
, vol.7
, pp. 471-474
-
-
Nacario, R.1
Kotakonda, S.2
Fouchard, D.M.D.3
Tillekeratne, L.M.V.4
Hudson, R.A.5
-
47
-
-
36849021012
-
One-pot reductive mono-N-alkylation of aniline and nitroarene derivatives using aldehydes
-
Byun, E.; Hong, B.; De Castro, K. A.; Lim, M.; Rhee, H. One-pot reductive mono-N-alkylation of aniline and nitroarene derivatives using aldehydes. J. Org. Chem. 2007, 72, 9815-9817.
-
(2007)
J. Org. Chem
, vol.72
, pp. 9815-9817
-
-
Byun, E.1
Hong, B.2
de Castro, K.A.3
Lim, M.4
Rhee, H.5
-
48
-
-
75749139686
-
The one-pot process for the preparation of N-monoalkyl aromatic amines from nitroarene derivatives
-
Jia, J. H.; Sheng, W. J.; Han, L.; Li, Y. J.; Gao, J. R.; Tu, J. F. The one-pot process for the preparation of N-monoalkyl aromatic amines from nitroarene derivatives. Sci. China Ser. B Chem. 2009, 52, 2171-2175.
-
(2009)
Sci. China Ser. B Chem
, vol.52
, pp. 2171-2175
-
-
Jia, J.H.1
Sheng, W.J.2
Han, L.3
Li, Y.J.4
Gao, J.R.5
Tu, J.F.6
-
49
-
-
33947152492
-
Reductive N-alkylation of aromatic amines and nitro compounds with ni-triles using polymethylhydrosiloxane
-
Reddy, C. R.; Vijeender, K.; Bhusan, P. B.; Madhavi, P. P.; Chandrasekhar, S. Reductive N-alkylation of aromatic amines and nitro compounds with ni-triles using polymethylhydrosiloxane. Tetrahedron Lett. 2007, 48, 2765-2768.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 2765-2768
-
-
Reddy, C.R.1
Vijeender, K.2
Bhusan, P.B.3
Madhavi, P.P.4
Chandrasekhar, S.5
-
50
-
-
38349062190
-
One-pot reductive monoalkylation of nitro aryls with hydrogen over Pd/C
-
Sydnes, M. O.; Isobe, M. One-pot reductive monoalkylation of nitro aryls with hydrogen over Pd/C. Tetrahedron Lett. 2008, 49, 1199-1202.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 1199-1202
-
-
Sydnes, M.O.1
Isobe, M.2
-
51
-
-
38449087357
-
Determination of solvent-trapped products obtained by photolysis of azides in 2,2,2-trifluoroethanol
-
Sydnes, M. O.; Doi, I.; Ohishi, A.; Kuse, M.; Isobe, M. Determination of solvent-trapped products obtained by photolysis of azides in 2,2,2-trifluoroethanol. Chem. Asian J. 2008, 3, 102-112.
-
(2008)
Chem. Asian J
, vol.3
, pp. 102-112
-
-
Sydnes, M.O.1
Doi, I.2
Ohishi, A.3
Kuse, M.4
Isobe, M.5
-
52
-
-
33947230753
-
Novel Pd/C-catalyzed re-dox reactions between aliphatic secondary alcohols and ketones under hy-drogenation conditions: Application to H-D exchange reaction and the mechanistic study
-
For mechanistic discussions see reference 52 and Sajiki, et al
-
For mechanistic discussions see reference 52 and Sajiki et al.; Esaki, H.; Ohtaki, R.; Maegawa, T.; Monguchi, Y.; Sajiki, H. Novel Pd/C-catalyzed re-dox reactions between aliphatic secondary alcohols and ketones under hy-drogenation conditions: Application to H-D exchange reaction and the mechanistic study. J. Org. Chem. 2007, 72, 2143-2150.
-
(2007)
J. Org. Chem
, vol.72
, pp. 2143-2150
-
-
Esaki, H.1
Ohtaki, R.2
Maegawa, T.3
Monguchi, Y.4
Sajiki, H.5
-
53
-
-
44349194250
-
Reductive monoalkylation of nitro aryls in one-pot
-
Sydnes, M. O.; Kuse, M.; Isobe, M. Reductive monoalkylation of nitro aryls in one-pot. Tetrahedron 2008, 64, 6406-6414.
-
(2008)
Tetrahedron
, vol.64
, pp. 6406-6414
-
-
Sydnes, M.O.1
Kuse, M.2
Isobe, M.3
-
54
-
-
54049150432
-
One-pot method to synthesize 4,6-bis(isopropylamino)-benzene-1,3-diol by catalytic reductive mono-N-alkylation of amine derivatives
-
Jin, Z.; Li, D.; Ma, R.; Peng, X.; Wang, X.; Lu, G. One-pot method to synthesize 4,6-bis(isopropylamino)-benzene-1,3-diol by catalytic reductive mono-N-alkylation of amine derivatives. Chin. J. Catal. 2008, 29, 878-880.
-
(2008)
Chin. J. Catal
, vol.29
, pp. 878-880
-
-
Jin, Z.1
Li, D.2
Ma, R.3
Peng, X.4
Wang, X.5
Lu, G.6
-
55
-
-
67349185941
-
One-pot method to synthesize 4,6-bis(isopropylamino)resorcinol through hydrodechlorination and catalyti-cally reductive mono-N-alkylation
-
Jin, Z.; Li, D.; Ma, R.; Peng X.; Wang, X.; Lu, G. One-pot method to synthesize 4,6-bis(isopropylamino)resorcinol through hydrodechlorination and catalyti-cally reductive mono-N-alkylation. J. Ind. Eng. Chem. 2009, 15, 434-437.
-
(2009)
J. Ind. Eng. Chem
, vol.15
, pp. 434-437
-
-
Jin, Z.1
Li, D.2
Ma, R.3
Peng, X.4
Wang, X.5
Lu, G.6
-
56
-
-
77952508741
-
Pd/C-catalyzed reductive mono-N-alkylation of nitrophenol derivatives in one-pot way
-
Zin, Z.; Li, D.; Wang, X.; Lu, G. Pd/C-catalyzed reductive mono-N-alkylation of nitrophenol derivatives in one-pot way. Chin. J. Chem. 2010, 28, 16-20.
-
(2010)
Chin. J. Chem
, vol.28
, pp. 16-20
-
-
Zin, Z.1
Li, D.2
Wang, X.3
Lu, G.4
-
57
-
-
70449629319
-
Directed one-pot reductive amination of aldehydes with nitroarenes in a domino fashion: Catalysis by gum-acacia-stabilized palladium nanoparticles
-
Sreedhar, B.; Reddy, P. S.; Devi, D. K. Directed one-pot reductive amination of aldehydes with nitroarenes in a domino fashion: Catalysis by gum-acacia-stabilized palladium nanoparticles. J. Org. Chem. 2009, 74, 8806-8809.
-
(2009)
J. Org. Chem
, vol.74
, pp. 8806-8809
-
-
Sreedhar, B.1
Reddy, P.S.2
Devi, D.K.3
-
58
-
-
77953123513
-
11C]PBR28, a PET biomarker for the peripheral benzodiazepine receptor
-
11C]PBR28, a PET biomarker for the peripheral benzodiazepine receptor. Tetrahedron Lett. 2010, 51, 3353-3355.
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 3353-3355
-
-
Hoareau, R.1
Scott, P.J.H.2
-
59
-
-
0030586164
-
Catalytic reductive N-alkylation of anilines. Application to the synthesis of N-aryl aminoacid precursors
-
Fache, F.; Valot, F.; Milenkovic, A.; Lemaire, M. Catalytic reductive N-alkylation of anilines. Application to the synthesis of N-aryl aminoacid precursors. Tetrahedron 1996, 52, 9777-9784.
-
(1996)
Tetrahedron
, vol.52
, pp. 9777-9784
-
-
Fache, F.1
Valot, F.2
Milenkovic, A.3
Lemaire, M.4
-
60
-
-
72249096260
-
First use of HEH in oxazine synthesis: Hydroxy-substituted 2H-1,4-benzoxazine derivatives
-
Meng, Q.; Liu, Q.; Li, J.; Xing, R.-G.; Shen, X.-X.; Zhou, B. First use of HEH in oxazine synthesis: Hydroxy-substituted 2H-1,4-benzoxazine derivatives. Synlett 2009, 3283-3286.
-
(2009)
Synlett
, pp. 3283-3286
-
-
Meng, Q.1
Liu, Q.2
Li, J.3
Xing, R.-G.4
Shen, X.-X.5
Zhou, B.6
-
61
-
-
34547187077
-
A general and practical method of alkynyl indole and benzofuran synthesis via tandem Cu- and Pd-catalyzed cross-couplings
-
Nagamochi, M.; Fang, Y.-Q.; Lautens, M. A general and practical method of alkynyl indole and benzofuran synthesis via tandem Cu- and Pd-catalyzed cross-couplings. Org. Lett. 2007, 9, 2955-2958.
-
(2007)
Org. Lett
, vol.9
, pp. 2955-2958
-
-
Nagamochi, M.1
Fang, Y.-Q.2
Lautens, M.3
-
62
-
-
37049107259
-
Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
-
Miyaura, N.; Suzuki, A. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst. J. Chem. Soc., Chem. Commun. 1979, 866-867.
-
(1979)
J. Chem. Soc., Chem. Commun
, pp. 866-867
-
-
Miyaura, N.1
Suzuki, A.2
-
63
-
-
49249152617
-
A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
-
Miyaura, N.; Yamada, K.; Suzuki, A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett. 1979, 20, 3437-3440.
-
(1979)
Tetrahedron Lett
, vol.20
, pp. 3437-3440
-
-
Miyaura, N.1
Yamada, K.2
Suzuki, A.3
-
64
-
-
34547230604
-
Heterogeneous Pd/C-catalyzed ligand-free, room-temperature Su-zuki-Miyaura coupling reactions in aqueous media
-
Maegawa, T.; Kitamura, Y.; Sako, S.; Udzu, T.; Sakurai, A.; Tanaka, A.; Kobayashi, Y.; Endo, K.; Bora, U.; Kurita, T.; Kozaki, A.; Monguchi, Y.; Sajiki, H. Heterogeneous Pd/C-catalyzed ligand-free, room-temperature Su-zuki-Miyaura coupling reactions in aqueous media. Chem. Eur. J. 2007, 13, 5937-5943.
-
(2007)
Chem. Eur. J
, vol.13
, pp. 5937-5943
-
-
Maegawa, T.1
Kitamura, Y.2
Sako, S.3
Udzu, T.4
Sakurai, A.5
Tanaka, A.6
Kobayashi, Y.7
Endo, K.8
Bora, U.9
Kurita, T.10
Kozaki, A.11
Monguchi, Y.12
Sajiki, H.13
-
65
-
-
34347352165
-
Polyaniline supported palladium catalyzed Suzuki-Miyaura cross-coupling of bromo- and chloroarenes in water
-
Kantam, M. L.; Roy, M.; Roy, S.; Sreedhar, B.; Madhavendra, S. S.; Chou-dary, B. M.; De, R. L. Polyaniline supported palladium catalyzed Suzuki-Miyaura cross-coupling of bromo- and chloroarenes in water. Tetrahedron 2007, 63, 8002-8009.
-
(2007)
Tetrahedron
, vol.63
, pp. 8002-8009
-
-
Kantam, M.L.1
Roy, M.2
Roy, S.3
Sreedhar, B.4
Madhavendra, S.S.5
Chou-Dary, B.M.6
De, R.L.7
-
66
-
-
35748965305
-
Palladium on carbon as a precatalyst for the Suzuki-Miyaura cross-coupling of aryl chlorides
-
Simeone, J. P.; Sowa, J. R. Palladium on carbon as a precatalyst for the Suzuki-Miyaura cross-coupling of aryl chlorides. Tetrahedron 2007, 63, 12646-12654.
-
(2007)
Tetrahedron
, vol.63
, pp. 12646-12654
-
-
Simeone, J.P.1
Sowa, J.R.2
-
67
-
-
70350518831
-
Microwave-assisted cross-coupling and hydrogenation chemistry by using heterogeneous transi-tion-metal catalysts: An evaluation of the role of selective catalyst heating
-
Irfan, M.; Fuchs, M.; Glasnov, T. N.; Kappe, C. O. Microwave-assisted cross-coupling and hydrogenation chemistry by using heterogeneous transi-tion-metal catalysts: An evaluation of the role of selective catalyst heating. Chem. Eur. J. 2009, 15, 11608-11618.
-
(2009)
Chem. Eur. J
, vol.15
, pp. 11608-11618
-
-
Irfan, M.1
Fuchs, M.2
Glasnov, T.N.3
Kappe, C.O.4
-
68
-
-
77349104068
-
Molecular sieves-supported palladium(II) catalyst: Suzuki coupling of chloroarenes and an easy access to useful intermediates for the synthesis of irbesartan, losartan and boscalid
-
Dey, R; Sreedhar, B.; Ranu, B. C. Molecular sieves-supported palladium(II) catalyst: Suzuki coupling of chloroarenes and an easy access to useful intermediates for the synthesis of irbesartan, losartan and boscalid. Tetrahedron 2010, 66, 2301-2305.
-
(2010)
Tetrahedron
, vol.66
, pp. 2301-2305
-
-
Dey, R.1
Sreedhar, B.2
Ranu, B.C.3
-
69
-
-
56249112339
-
Radiolytic synthesis of Pd-M (M = Ag, Ni, and Cu)/C catalyst and their use in Suzuki-type and Heck-type reaction
-
Kim, S.-J.; Oh, S.-D.; Lee, S.; Choi, S.-H. Radiolytic synthesis of Pd-M (M = Ag, Ni, and Cu)/C catalyst and their use in Suzuki-type and Heck-type reaction. J. Ind. Eng. Chem. 2008, 14, 449-456.
-
(2008)
J. Ind. Eng. Chem
, vol.14
, pp. 449-456
-
-
Kim, S.-J.1
Oh, S.-D.2
Lee, S.3
Choi, S.-H.4
-
70
-
-
52949124507
-
Sulphonated "click" dendrimer stabilized palladium nanoparticles as highly efficient catalysts for olefin hydrogenation and Suzuki coupling reactions under ambient conditions in aqueous media
-
Ornelas, C; Ruiz, J.; Salmon, L.; Astruc, D. Sulphonated "click" dendrimer stabilized palladium nanoparticles as highly efficient catalysts for olefin hydrogenation and Suzuki coupling reactions under ambient conditions in aqueous media. Adv. Synth. Catal 2008, 350, 837-845.
-
(2008)
Adv. Synth. Catal
, vol.350
, pp. 837-845
-
-
Ornelas, C.1
Ruiz, J.2
Salmon, L.3
Astruc, D.4
-
71
-
-
53849094780
-
-
Wu, L.; Li, Z.-W.; Zhang, F.; He, Y.-M.; Fan, Q.-H. Air-stable and highly active dendritic phosphine oxide-stabilized palladium nanoparticles: Preparation, characterization and applications in the carbon-carbon bond formation and hydrogenation reactions. Adv. Synth. Catal 2008, 350, 846-862.
-
(2008)
Air-stable and Highly Active Dendritic Phosphine Oxide-stabilized Palladium Nanoparticles: Preparation, Characterization and Applications In the Carbon-carbon Bond Formation and Hydrogenation Reactions
, vol.350
, pp. 846-862
-
-
Wu, L.1
Li, Z.-W.2
Zhang, F.3
He, Y.-M.4
Fan, Q.-H.5
-
72
-
-
68949131086
-
Palladium-containing hypercrosslinked polystyrene as an easy to prepare catalyst for Suzuki reaction in water and organic solvents
-
Lyubimov, S. E.; Vasil'ev, A. A.; Korlyukov, A. A.; Ilyin, M. M.; Pisarev, S. A.; Matveev, V. V.; Chalykh, A. E.; Zlotin, S. G.; Davankov, V. A. Palladium-containing hypercrosslinked polystyrene as an easy to prepare catalyst for Suzuki reaction in water and organic solvents. React. Funct. Polym. 2009, 69, 755-758.
-
(2009)
React. Funct. Polym
, vol.69
, pp. 755-758
-
-
Lyubimov, S.E.1
Vasil'ev, A.A.2
Korlyukov, A.A.3
Ilyin, M.M.4
Pisarev, S.A.5
Matveev, V.V.6
Chalykh, A.E.7
Zlotin, S.G.8
Davankov, V.A.9
-
73
-
-
45649085365
-
Efficient heterogeneous vinylation of aryl halides using potassium vinyltrifluoroborate
-
Joucla, L.; Cusati, G.; Pinel, C.; Djakovitch, L. Efficient heterogeneous vinylation of aryl halides using potassium vinyltrifluoroborate. Tetrahedron Lett. 2008, 49, 4738-4741.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 4738-4741
-
-
Joucla, L.1
Cusati, G.2
Pinel, C.3
Djakovitch, L.4
-
74
-
-
65449177310
-
Heterogeneously Pd/C catalysed procedure for the vinylation of aryl bromides
-
Joucla, L.; Cusati, G.; Pinel, C.; Djakovitch, L. Heterogeneously Pd/C catalysed procedure for the vinylation of aryl bromides. App. Catal. A: Gen. 2009, 360, 145-153.
-
(2009)
App. Catal. A: Gen
, vol.360
, pp. 145-153
-
-
Joucla, L.1
Cusati, G.2
Pinel, C.3
Djakovitch, L.4
-
75
-
-
81155147379
-
-
For an excellent description of eggshell and uniform Pd/C, see reference 4
-
For an excellent description of eggshell and uniform Pd/C, see reference 4.
-
-
-
-
76
-
-
62649098697
-
Improved Suzuki-Miyaura reactions of aryldiazonium salts with boronic acids by tuning palladium on charcoal catalyst properties
-
Felpin, F.-X.; Fouquet, E.; Zakri, C. Improved Suzuki-Miyaura reactions of aryldiazonium salts with boronic acids by tuning palladium on charcoal catalyst properties. Adv. Synth. Catal 2009, 351, 649-655.
-
(2009)
Adv. Synth. Catal
, vol.351
, pp. 649-655
-
-
Felpin, F.-X.1
Fouquet, E.2
Zakri, C.3
-
77
-
-
33846263624
-
Regioselective construction of six-membered fused heterocyclic rings via Pd/C-mediated C-C coupling followed by iodocyclization strategy: A new entry to 2H-1,2-benzothiazine-1,1-dioxides
-
Barange, D. K.; Batchu, V. R.; Gorja, D.; Pattabiraman, V. R.; Tatini, L. K.; Babu, J. M.; Pal, M. Regioselective construction of six-membered fused heterocyclic rings via Pd/C-mediated C-C coupling followed by iodocyclization strategy: A new entry to 2H-1,2-benzothiazine-1,1-dioxides. Tetrahedron 2007, 63, 1775-1789.
-
(2007)
Tetrahedron
, vol.63
, pp. 1775-1789
-
-
Barange, D.K.1
Batchu, V.R.2
Gorja, D.3
Pattabiraman, V.R.4
Tatini, L.K.5
Babu, J.M.6
Pal, M.7
-
78
-
-
36148965545
-
Pd/C-catalyzed alkynylation of p-chloroacroleins
-
Bera, R; Swamy, N. K.; Dhananjaya, G.; Babu, J. M.; Kumar, P. R.; Kukkanti, K.; Pal, M. Pd/C-catalyzed alkynylation of p-chloroacroleins. Tetrahe-dron 2007, 63, 13018-13023.
-
(2007)
Tetrahe-dron
, vol.63
, pp. 13018-13023
-
-
Bera, R.1
Swamy, N.K.2
Dhananjaya, G.3
Babu, J.M.4
Kumar, P.R.5
Kukkanti, K.6
Pal, M.7
-
79
-
-
45449096265
-
Synthesis of 2-alkynylquinolines from 2-chloro and 2,4-dichloroquinoline via Pd/C-catalyzed coupling reaction in water
-
Reddy, E. A.; Barange, D. K.; Islam, A.; Mukkanti, K.; Pal, M. Synthesis of 2-alkynylquinolines from 2-chloro and 2,4-dichloroquinoline via Pd/C-catalyzed coupling reaction in water. Tetrahedron 2008, 64, 7143-7150.
-
(2008)
Tetrahedron
, vol.64
, pp. 7143-7150
-
-
Reddy, E.A.1
Barange, D.K.2
Islam, A.3
Mukkanti, K.4
Pal, M.5
-
80
-
-
67649877969
-
C-N bond forming reaction under copper catalysis: A new synthesis of 2-substituted 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolines
-
Layek, M.; Rao, A. V. D.; Gajare, V.; Kalita, D.; Barange, D. K.; Islam, A.; Mukkanti, K.; Pal, M. C-N bond forming reaction under copper catalysis: A new synthesis of 2-substituted 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolines. Tetrahedron Lett. 2009, 50, 4878-4881.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4878-4881
-
-
Layek, M.1
Rao, A.V.D.2
Gajare, V.3
Kalita, D.4
Barange, D.K.5
Islam, A.6
Mukkanti, K.7
Pal, M.8
-
81
-
-
75949085563
-
Regioselective alkynylation followed by Suzuki coupling of 2,4-dichloroquinoline: Synthesis of 2-alkynyl-4-arylquinolines
-
Reddy, E. A.; Islam, A.; Mukkanti, K.; Bandameedi, V.; Bhowmik, D. R; Pal, M. Regioselective alkynylation followed by Suzuki coupling of 2,4-dichloroquinoline: Synthesis of 2-alkynyl-4-arylquinolines. Beilstein J. Org. Chem. 2009, 5, No. 32.
-
(2009)
Beilstein J. Org. Chem
, vol.32
, pp. 5
-
-
Reddy, E.A.1
Islam, A.2
Mukkanti, K.3
Bandameedi, V.4
Bhowmik, D.R.5
Pal, M.6
-
82
-
-
37049020933
-
A simple and efficient recyclable phosphine-free catalytic system for alkoxycarbonylation and carbonylative Sonogashira coupling reactions of aryl iodides
-
Liu, J.; Chen, J.; Xia, C. A simple and efficient recyclable phosphine-free catalytic system for alkoxycarbonylation and carbonylative Sonogashira coupling reactions of aryl iodides. J. Catal 2008, 253, 50-56.
-
(2008)
J. Catal
, vol.253
, pp. 50-56
-
-
Liu, J.1
Chen, J.2
Xia, C.3
-
83
-
-
55549115353
-
Copper-free Sonoga-shira coupling of acid chlorides with terminal alkynes in the presence of reusable palladium catalyst: An improved synthesis of 3-iodochromenones (= 3-iodo-4H-1-benzopyran-4-ones)
-
Likhar, P. R; Subhas, M. S.; Roy, M.; Kantam, M. L. Copper-free Sonoga-shira coupling of acid chlorides with terminal alkynes in the presence of reusable palladium catalyst: An improved synthesis of 3-iodochromenones (= 3-iodo-4H-1-benzopyran-4-ones). Helv. Chim. Acta 2008, 91, 259-264.
-
(2008)
Helv. Chim. Acta
, vol.91
, pp. 259-264
-
-
Likhar, P.R.1
Subhas, M.S.2
Roy, M.3
Kantam, M.L.4
-
84
-
-
53849112664
-
Ligand-free Sonogashira coupling reactions with heterogeneous Pd/C as the catalyst
-
Mori, S.; Yanase, T.; Aoyagi, S.; Monguchi, Y.; Maegawa, T.; Sajiki, H. Ligand-free Sonogashira coupling reactions with heterogeneous Pd/C as the catalyst. Chem. Eur. J. 2008, 14, 6994-6999.
-
(2008)
Chem. Eur. J
, vol.14
, pp. 6994-6999
-
-
Mori, S.1
Yanase, T.2
Aoyagi, S.3
Monguchi, Y.4
Maegawa, T.5
Sajiki, H.6
-
85
-
-
77649275164
-
Heterogeneous Suzuki and copper-free Sonogashira cross-coupling reactions catalyzed by a reusable palladium(II) complex in water medium
-
Islam, S. M.; Mondal, P.; Roy, A. S.; Mondal, S.; Hossain, D. Heterogeneous Suzuki and copper-free Sonogashira cross-coupling reactions catalyzed by a reusable palladium(II) complex in water medium. Tetrahedron Lett. 2010, 51, 2067-2070.
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 2067-2070
-
-
Islam, S.M.1
Mondal, P.2
Roy, A.S.3
Mondal, S.4
Hossain, D.5
-
86
-
-
77949294177
-
UC Pd: A new form of Pd/C for Sonogashira couplings
-
Duplais, C.; Forman, A. J.; Baker, B. A.; Lipshutz, B. H. UC Pd: A new form of Pd/C for Sonogashira couplings. Chem. Eur. J. 2010, 16, 3366-3371.
-
(2010)
Chem. Eur. J
, vol.16
, pp. 3366-3371
-
-
Duplais, C.1
Forman, A.J.2
Baker, B.A.3
Lipshutz, B.H.4
-
87
-
-
0034832488
-
Heck reaction catalyzed by Pd-modified zeolites
-
For the prepartion of this catalyst, see
-
For the prepartion of this catalyst, see: Djakovitch, L.; Koehler, K. Heck reaction catalyzed by Pd-modified zeolites. J. Am. Chem. Soc. 2001, 123, 5990-5999.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 5990-5999
-
-
Djakovitch, L.1
Koehler, K.2
-
88
-
-
34547179974
-
Efficient heterogeneously palla-dium-catalysed Heck arylation of acrolein diethyl acetal. Selective synthesis of cinnamaldehydes or 3-arylpropionic esters
-
Noël, S.; Luo, C.; Pinel, C.; Djakovitch, L. Efficient heterogeneously palla-dium-catalysed Heck arylation of acrolein diethyl acetal. Selective synthesis of cinnamaldehydes or 3-arylpropionic esters. Adv. Synth. Catal 2007, 349, 1128-1140.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 1128-1140
-
-
Noël, S.1
Luo, C.2
Pinel, C.3
Djakovitch, L.4
-
89
-
-
65949112475
-
Synthesis of 3-arylpropenal and 3-arylpropionic acids by palladium catalysed Heck coupling reactions: Scopes and limitations
-
Djakovitch, L.; Pinel, C. Synthesis of 3-arylpropenal and 3-arylpropionic acids by palladium catalysed Heck coupling reactions: Scopes and limitations. Curr. Org. Synth. 2009, 6, 54-65.
-
(2009)
Curr. Org. Synth
, vol.6
, pp. 54-65
-
-
Djakovitch, L.1
Pinel, C.2
-
90
-
-
67650395937
-
Efficient heterogeneously palladium-catalysed synthesis of stilbenes and bibenzyls
-
Cusati, G.; Wedig, A.; Djakovitch, L. Efficient heterogeneously palladium-catalysed synthesis of stilbenes and bibenzyls. Lett. Org. Chem. 2009, 6, 77-81.
-
(2009)
Lett. Org. Chem
, vol.6
, pp. 77-81
-
-
Cusati, G.1
Wedig, A.2
Djakovitch, L.3
-
91
-
-
35948935229
-
Heck reactions with very low ligandless catalyst loads accelerated by microwaves or simultaneous microwaves/ultrasound irradiation
-
Palmisano, G.; Bonrath, W.; Boffa, L.; Garella, D.; Barge, A.; Cravotto, G. Heck reactions with very low ligandless catalyst loads accelerated by microwaves or simultaneous microwaves/ultrasound irradiation. Adv. Synth. Catal. 2007, 349, 2338-2344.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 2338-2344
-
-
Palmisano, G.1
Bonrath, W.2
Boffa, L.3
Garella, D.4
Barge, A.5
Cravotto, G.6
-
92
-
-
56649122065
-
Heck cross-coupling of aryldiazonium tetrafluoroborate with acrylates catalyzed by palladium on charcoal
-
Felpin, F.-X.; Fouquet, E.; Zakri, C. Heck cross-coupling of aryldiazonium tetrafluoroborate with acrylates catalyzed by palladium on charcoal. Adv. Synth. Catal. 2008, 350, 2559-2565.
-
(2008)
Adv. Synth. Catal
, vol.350
, pp. 2559-2565
-
-
Felpin, F.-X.1
Fouquet, E.2
Zakri, C.3
-
93
-
-
67650493000
-
Heterogeneous palladium mulit-task catalyst for sequential Heck-reduction-cyclization (HRC) reactions: Influence of the support
-
Ibarguren, O.; Zakri, C.; Fouquet, E.; Felpin, F.-X. Heterogeneous palladium mulit-task catalyst for sequential Heck-reduction-cyclization (HRC) reactions: Influence of the support. Tetrahedron Lett. 2009, 50, 5071-5074.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 5071-5074
-
-
Ibarguren, O.1
Zakri, C.2
Fouquet, E.3
Felpin, F.-X.4
-
94
-
-
33846213874
-
Heck coupling in zeolitic microcapsular reactor: A test for encaged quasi-homogeneous catalysis
-
Ren, N.; Yang, Y.-H.; Zhang, Y.-H.; Wang, Q.-R.; Tang, Y. Heck coupling in zeolitic microcapsular reactor: A test for encaged quasi-homogeneous catalysis. J. Catal. 2007, 246, 215-222.
-
(2007)
J. Catal
, vol.246
, pp. 215-222
-
-
Ren, N.1
Yang, Y.-H.2
Zhang, Y.-H.3
Wang, Q.-R.4
Tang, Y.5
-
95
-
-
39249083546
-
Chemically modified cyclodextrins adsorbed on Pd/C particles: New opportunities to generate highly chemo- and stereoselective catalysts for Heck reaction
-
Cassez, A.; Kania, N.; Hapiot, F.; Fourmentin, S.; Monflier, E.; Ponchel, A. Chemically modified cyclodextrins adsorbed on Pd/C particles: New opportunities to generate highly chemo- and stereoselective catalysts for Heck reaction. Catal. Commun. 2008, 9, 1346-1351.
-
(2008)
Catal. Commun
, vol.9
, pp. 1346-1351
-
-
Cassez, A.1
Kania, N.2
Hapiot, F.3
Fourmentin, S.4
Monflier, E.5
Ponchel, A.6
-
96
-
-
57649153127
-
The heterogeneous catalytic Heck reaction in an ionic liauid
-
Aslanov, L. A.; Valetskii, P. M.; Volkov, V. V.; Zakharov, V. N.; Kabachii, Y. A.; Kochev, S. Y.; Romanvskii, B. V.; Yatsenko, A. V. The heterogeneous catalytic Heck reaction in an ionic liauid. Russ. J. Phys. Chem. A 2008, 82, 2238-2242.
-
(2008)
Russ. J. Phys. Chem. A
, vol.82
, pp. 2238-2242
-
-
Aslanov, L.A.1
Valetskii, P.M.2
Volkov, V.V.3
Zakharov, V.N.4
Kabachii, Y.A.5
Kochev, S.Y.6
Romanvskii, B.V.7
Yatsenko, A.V.8
-
97
-
-
15744367106
-
Ionic liquids: Solvent properties and organic reactivity
-
Chiappe, C.; Pieraccini, D. Ionic liquids: Solvent properties and organic reactivity. J. Phys. Org. Chem. 2005, 18, 275-297.
-
(2005)
J. Phys. Org. Chem
, vol.18
, pp. 275-297
-
-
Chiappe, C.1
Pieraccini, D.2
-
98
-
-
33644806022
-
Functionalized imidazolium salts for task-specific ionic liquids and their applications
-
Lee, S. Functionalized imidazolium salts for task-specific ionic liquids and their applications. Chem. Commun. 2006, 1049-1063.
-
(2006)
Chem. Commun
, pp. 1049-1063
-
-
Lee, S.1
-
99
-
-
33644749212
-
From dysfunction to bis-function: On the design and applications of functionalized ionic liquids
-
Fei, Z.; Geldbach, T. J.; Zhao, D.; Dyson, P. J. From dysfunction to bis-function: On the design and applications of functionalized ionic liquids. Chem. Eur. J. 2006, 12, 2122-2130.
-
(2006)
Chem. Eur. J
, vol.12
, pp. 2122-2130
-
-
Fei, Z.1
Geldbach, T.J.2
Zhao, D.3
Dyson, P.J.4
-
100
-
-
24944519864
-
Palladium catalysts
-
and references cited therein
-
Mozingo, R. Palladium catalysts. Org. Synth. 1946, 26, 77-81 and references cited therein.
-
(1946)
Org. Synth
, vol.26
, pp. 77-81
-
-
Mozingo, R.1
-
101
-
-
71849111363
-
Recent advances in the design and use of immobilized N-heterocyclic carbene ligands for transition-metal catalysis
-
Cazin, C. S. J. Recent advances in the design and use of immobilized N-heterocyclic carbene ligands for transition-metal catalysis. C. R. Chimie 2009, 12, 1173-1180.
-
(2009)
C. R. Chimie
, vol.12
, pp. 1173-1180
-
-
Cazin, C.S.J.1
-
102
-
-
0034684710
-
Investigation of the palladium catalyzed aromatic coupling of pyridine derivatives
-
Hagelin, H.; Hedman, B.; Orabona, I.; Åkermark, T.; Åkermark, B.; Klug, C. A. Investigation of the palladium catalyzed aromatic coupling of pyridine derivatives. J. Mol. Catal. A Chem. 2000, 164, 137-146.
-
(2000)
J. Mol. Catal. a Chem
, vol.164
, pp. 137-146
-
-
Hagelin, H.1
Hedman, B.2
Orabona, I.3
Åkermark, T.4
Åkermark, B.5
Klug, C.A.6
-
103
-
-
40849119489
-
C-H activation and C-C coupling of 4-methylpyridine using palladium supported on nanoparticle alumina
-
Neal, L. M.; Hagelin-Weaver, H. C-H activation and C-C coupling of 4-methylpyridine using palladium supported on nanoparticle alumina. J. Mol. Catal. A Chem. 2008, 284, 141-148.
-
(2008)
J. Mol. Catal. a Chem
, vol.284
, pp. 141-148
-
-
Neal, L.M.1
Hagelin-Weaver, H.2
-
104
-
-
67349167425
-
Effects of nanoparticle and porous metal oxide supports on the activity of palladium catalysts in the oxidative coupling of 4-methylpyridine
-
Neal, L. M.; Hernandez, D.; Hagelin-Weaver, H. E. Effects of nanoparticle and porous metal oxide supports on the activity of palladium catalysts in the oxidative coupling of 4-methylpyridine. J. Mol. Catal. A: Chem. 2009, 307, 29-36.
-
(2009)
J. Mol. Catal. A: Chem
, vol.307
, pp. 29-36
-
-
Neal, L.M.1
Hernandez, D.2
Hagelin-Weaver, H.E.3
-
105
-
-
33746777755
-
An asymmetric catalyst
-
Akabori, S.; Skurai, S.; Izumi, Y.; Fujii, Y. An asymmetric catalyst. Nature 1956, 178, 323-324.
-
(1956)
Nature
, vol.178
, pp. 323-324
-
-
Akabori, S.1
Skurai, S.2
Izumi, Y.3
Fujii, Y.4
-
106
-
-
0038376570
-
Studies on the silk-palladium catalyst. I. Preparation and stability
-
Izumi, Y. studies on the silk-palladium catalyst. I. Preparation and stability. Bull. Chem. Soc. Jpn. 1959, 32, 932-936.
-
(1959)
Bull. Chem. Soc. Jpn
, vol.32
, pp. 932-936
-
-
Izumi, Y.1
-
107
-
-
0038376570
-
Studies on the silk-palladium catalyst. II. General properties
-
Izumi, Y. Studies on the silk-palladium catalyst. II. General properties. Bull. Chem. Soc. Jpn. 1959, 32, 936-942.
-
(1959)
Bull. Chem. Soc. Jpn
, vol.32
, pp. 936-942
-
-
Izumi, Y.1
-
108
-
-
0038376570
-
Studies on the silk-palladium catalyst. III
-
Izumi, Y. Studies on the silk-palladium catalyst. III. Bull. Chem. Soc. Jpn. 1959, 32, 942-945.
-
(1959)
Bull. Chem. Soc. Jpn
, vol.32
, pp. 942-945
-
-
Izumi, Y.1
-
109
-
-
0037213015
-
Preparation of silk fibroin-supported Pd(0) catalyst for chemoselective hydrogenation: Reduction of palladium(II) acetate by methanol on the protein
-
and references cited therein
-
Sajiki, H.; Ikawa, T.; Yamada, H.; Tsubouchi, K.; Hirota, K. Preparation of silk fibroin-supported Pd(0) catalyst for chemoselective hydrogenation: Reduction of palladium(II) acetate by methanol on the protein. Tetrahedron Lett. 2003, 44, 171-174 and references cited therein.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 171-174
-
-
Sajiki, H.1
Ikawa, T.2
Yamada, H.3
Tsubouchi, K.4
Hirota, K.5
-
110
-
-
0141922092
-
Markedly chemoselective hydrogenation with retention of benzyl ester and N-Cbz functions using a heterogeneous Pd-fibroin catalyst
-
Sajiki, H.; Ikawa, T.; Hirota, K. Markedly chemoselective hydrogenation with retention of benzyl ester and N-Cbz functions using a heterogeneous Pd-fibroin catalyst. Tetrahedron Lett. 2003, 44, 8437-8439.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 8437-8439
-
-
Sajiki, H.1
Ikawa, T.2
Hirota, K.3
-
111
-
-
53849127531
-
0-polyethyleneimine catalyst
-
0-polyethyleneimine catalyst. Chem. Eur. J. 2008, 14, 5109-5111.
-
(2008)
Chem. Eur. J
, vol.14
, pp. 5109-5111
-
-
Sajiki, H.1
Mori, S.2
Ohkubo, T.3
Ikawa, T.4
Kume, A.5
Maegawa, T.6
Monguchi, Y.7
-
112
-
-
67349277679
-
Pd(0)-polyethyleneimine complex as a partial hydrogenation catalyst of alkynes to alkenes
-
Mori, S.; Ohkubo, T.; Ikawa, T.; Kume, A.; Maegawa, T.; Monguchi, Y.; Sajiki, H. Pd(0)-polyethyleneimine complex as a partial hydrogenation catalyst of alkynes to alkenes. J. Mol. Catal. A Chem. 2009, 307, 77-87.
-
(2009)
J. Mol. Catal. a Chem
, vol.307
, pp. 77-87
-
-
Mori, S.1
Ohkubo, T.2
Ikawa, T.3
Kume, A.4
Maegawa, T.5
Monguchi, Y.6
Sajiki, H.7
-
113
-
-
58449124884
-
A highly active heterogeneous palladium catalyst supported on a synthetic adsorbent
-
Monguchi, Y.; Fujita, Y.; Endo, K.; Takao, S.; Yoshimura, M.; Takagi, Y.; Maegawa, T.; Sajiki, H. A highly active heterogeneous palladium catalyst supported on a synthetic adsorbent. Chem. Eur. J. 2009, 15, 834-837.
-
(2009)
Chem. Eur. J
, vol.15
, pp. 834-837
-
-
Monguchi, Y.1
Fujita, Y.2
Endo, K.3
Takao, S.4
Yoshimura, M.5
Takagi, Y.6
Maegawa, T.7
Sajiki, H.8
-
114
-
-
70349425800
-
Development of molecular sieves-supported palladium catalyst and chemoselective hydrogenation of unsaturated bonds in the presence of nitro groups
-
Maegawa, T.; Takahashi, T.; Yoshimura, M.; Suzuka, H.; Monguchi, Y.; Sajiki, H. Development of molecular sieves-supported palladium catalyst and chemoselective hydrogenation of unsaturated bonds in the presence of nitro groups. Adv. Synth. Catal. 2009, 351, 2091-2095.
-
(2009)
Adv. Synth. Catal
, vol.351
, pp. 2091-2095
-
-
Maegawa, T.1
Takahashi, T.2
Yoshimura, M.3
Suzuka, H.4
Monguchi, Y.5
Sajiki, H.6
-
115
-
-
77449115911
-
Palladium supported on polyether-functionalized mesoporous silica. Synthesis and application as catalyst for Heck coupling reaction
-
Grandsire, A. F.; Laborde, C.; Lamaty, F.; Mehdi, A. Palladium supported on polyether-functionalized mesoporous silica. Synthesis and application as catalyst for Heck coupling reaction. Appl. Organomet. Chem. 2010, 24, 179-183.
-
(2010)
Appl. Organomet. Chem
, vol.24
, pp. 179-183
-
-
Grandsire, A.F.1
Laborde, C.2
Lamaty, F.3
Mehdi, A.4
-
116
-
-
70350765028
-
Periodic mesoporous silica-immobilized palladium(II) complex as an effective and reusable catalyst for water-medium carbon-carbon coupling reactions
-
Kang, C.; Huang, J.; He, W.; Zhang, F. Periodic mesoporous silica-immobilized palladium(II) complex as an effective and reusable catalyst for water-medium carbon-carbon coupling reactions. J. Organomet. Chem. 2010, 695, 120-127.
-
(2010)
J. Organomet. Chem
, vol.695
, pp. 120-127
-
-
Kang, C.1
Huang, J.2
He, W.3
Zhang, F.4
-
117
-
-
77749240472
-
A recyclable nanoparticle-supported palladium catalyst for the hydroxycarbonylation of aryl halides in water
-
Wittmann, S.; Schätz, A.; Grass, R. N.; Stark, W. J.; Reiser, O. A recyclable nanoparticle-supported palladium catalyst for the hydroxycarbonylation of aryl halides in water. Angew. Chem. Int. Ed. 2010, 49, 1867-1870.
-
(2010)
Angew. Chem. Int. Ed
, vol.49
, pp. 1867-1870
-
-
Wittmann, S.1
Schätz, A.2
Grass, R.N.3
Stark, W.J.4
Reiser, O.5
-
118
-
-
77952409644
-
Magnetically separable nanocata-lysts: Bridges between homogeneous and heterogeneous catalysis
-
Shylesh, S.; Schünemann, V.; Thiel, W. R. Magnetically separable nanocata-lysts: Bridges between homogeneous and heterogeneous catalysis. Angew. Chem. Int. Ed. 2010, 49, 3428-3459.
-
(2010)
Angew. Chem. Int. Ed
, vol.49
, pp. 3428-3459
-
-
Shylesh, S.1
Schünemann, V.2
Thiel, W.R.3
-
119
-
-
60949095624
-
Preparation of super-paramagnetic magnetite nanoparticles by reverse precipitation method: Contribution of sonochemically generated oxidants
-
Mizukoshi, Y.; Shuto, T.; Masahashi, N.; Tanabe, S. Preparation of super-paramagnetic magnetite nanoparticles by reverse precipitation method: Contribution of sonochemically generated oxidants. Ultrason. Sonochem. 2009, 16, 525-531.
-
(2009)
Ultrason. Sonochem
, vol.16
, pp. 525-531
-
-
Mizukoshi, Y.1
Shuto, T.2
Masahashi, N.3
Tanabe, S.4
-
120
-
-
53649085278
-
Magnetically retievable palladium/maghemite nanocomposite catalysts prepared by sonochemical reduction method
-
Mizukoshi, Y.; Sato, K.; Konno, T. J.; Masahashi, N.; Tanabe, S. Magnetically retievable palladium/maghemite nanocomposite catalysts prepared by sonochemical reduction method. Chem. Lett. 2008, 37, 922-923.
-
(2008)
Chem. Lett
, vol.37
, pp. 922-923
-
-
Mizukoshi, Y.1
Sato, K.2
Konno, T.J.3
Masahashi, N.4
Tanabe, S.5
-
121
-
-
57549094447
-
Facile Suzuki coupling over ortho-metalated palladium(II) complex anchored on 2D-hexagonal mesoporous organosilica
-
Sarkar, K.; Nandi, M.; Islam, M.; Mubarak, M.; Bhaumik, A. Facile Suzuki coupling over ortho-metalated palladium(II) complex anchored on 2D-hexagonal mesoporous organosilica. App. Catal. A: Gen. 2009, 352, 81-86.
-
(2009)
App. Catal. A: Gen
, vol.352
, pp. 81-86
-
-
Sarkar, K.1
Nandi, M.2
Islam, M.3
Mubarak, M.4
Bhaumik, A.5
-
122
-
-
53749104612
-
Optically active (peptido-carbene)palladium complexes: Towards true solid-phase combinatorial libraries of transition metal catalysts
-
Jensen, J. F.; Worm-Leonhard, K.; Meldal, M. Optically active (peptido-carbene)palladium complexes: Towards true solid-phase combinatorial libraries of transition metal catalysts. Eur. J. Org. Chem. 2008, 3785-3797.
-
(2008)
Eur. J. Org. Chem
, pp. 3785-3797
-
-
Jensen, J.F.1
Worm-Leonhard, K.2
Meldal, M.3
-
123
-
-
55049101760
-
Green catalysts: Solid-phase peptide car-bene ligands in aqueous transition-metal catalysis
-
Worm-Leonhard, K.; Meldal, M. Green catalysts: Solid-phase peptide car-bene ligands in aqueous transition-metal catalysis. Eur. J. Org. Chem. 2008, 5244-5253.
-
(2008)
Eur. J. Org. Chem
, pp. 5244-5253
-
-
Worm-Leonhard, K.1
Meldal, M.2
-
124
-
-
20444409746
-
Preparation of polystyrene-supported soluble palladacycle catalyst for Heck and Suzuki reactions
-
Luo, F.-T.; Xue, C.; Ko, S.-L.; Shao, Y.-D.; Wu, C.-J.; Kuo, Y.-M. Preparation of polystyrene-supported soluble palladacycle catalyst for Heck and Suzuki reactions. Tetrahedron 2005, 61, 6040-6045.
-
(2005)
Tetrahedron
, vol.61
, pp. 6040-6045
-
-
Luo, F.-T.1
Xue, C.2
Ko, S.-L.3
Shao, Y.-D.4
Wu, C.-J.5
Kuo, Y.-M.6
-
125
-
-
73149083510
-
Copper-free Sonogashira coupling in water with an amphiphilic resin-supported palladium complex
-
Suzuka, T.; Okada, Y.; Ooshiro, K.; Uozumi, Y. Copper-free Sonogashira coupling in water with an amphiphilic resin-supported palladium complex. Tetrahedron 2010, 66, 1064-1069.
-
(2010)
Tetrahedron
, vol.66
, pp. 1064-1069
-
-
Suzuka, T.1
Okada, Y.2
Ooshiro, K.3
Uozumi, Y.4
-
126
-
-
57749098680
-
On the immobilization of catechol phosphane palladium complexes on titania
-
Chikkali, S.; Gudat, D.; Mallissery, S. K. On the immobilization of catechol phosphane palladium complexes on titania. Eur. J. Inorg. Chem. 2008, 5603-5608.
-
(2008)
Eur. J. Inorg. Chem
, pp. 5603-5608
-
-
Chikkali, S.1
Gudat, D.2
Mallissery, S.K.3
-
127
-
-
60849113460
-
An immobilized ortho-palladated dimethylbenzylamine complex as an efficient catalyst for the methanolysis of phosphorothionate pesticides
-
Mohamed, M. F.; Neverov, A. A.; Brown, R. S. An immobilized ortho-palladated dimethylbenzylamine complex as an efficient catalyst for the methanolysis of phosphorothionate pesticides. Inorg. Chem. 2009, 48, 1183-1191.
-
(2009)
Inorg. Chem
, vol.48
, pp. 1183-1191
-
-
Mohamed, M.F.1
Neverov, A.A.2
Brown, R.S.3
-
128
-
-
77953669854
-
Catalysis in carbon nanotubes
-
Serp, P.; Castillejos, E. Catalysis in carbon nanotubes. ChemCatChem 2010, 2, 41-47.
-
(2010)
ChemCatChem
, vol.2
, pp. 41-47
-
-
Serp, P.1
Castillejos, E.2
-
129
-
-
0344468123
-
Mesoporous carbon nanotubes for use as support in catalysis and as nanosized reactors for one-dimensional inorganic material synthesis
-
Nhut, J.-M.; Pesant, L.; Tessonnier, J.-P.; Winé, G.; Guille, J.; Pham-Huu, C.; Ledoux, M.-J. Mesoporous carbon nanotubes for use as support in catalysis and as nanosized reactors for one-dimensional inorganic material synthesis. Appl. Catal. A Gen. 2003, 254, 345-363.
-
(2003)
Appl. Catal. a Gen
, vol.254
, pp. 345-363
-
-
Nhut, J.-M.1
Pesant, L.2
Tessonnier, J.-P.3
Winé, G.4
Guille, J.5
Pham-Huu, C.6
Ledoux, M.-J.7
-
130
-
-
44449142058
-
Naga-shima, H. Chemoselective hydrogenation of nitroarenes with carbon nanofi-ber-supported platinum and palladium nanoparticles
-
Takasaki, M.; Motoyama, Y.; Higashi, K.; Yoon, S.-H.; Mochida, I.; Naga-shima, H. Chemoselective hydrogenation of nitroarenes with carbon nanofi-ber-supported platinum and palladium nanoparticles. Org. Lett. 2008, 10, 1601-1604.
-
(2008)
Org. Lett
, vol.10
, pp. 1601-1604
-
-
Takasaki, M.1
Motoyama, Y.2
Higashi, K.3
Yoon, S.-H.4
Mochida, I.5
-
132
-
-
0004196433
-
-
In Nanoscale Materials in Chemistry, Klabunde, K. J., Ed.; Wiley-Interscience: New York
-
Schmid, G. In Nanoscale Materials in Chemistry, Klabunde, K. J., Ed.; Wiley-Interscience: New York, 2001; pp. 15-59.
-
(2001)
, pp. 15-59
-
-
Schmid, G.1
-
133
-
-
77949697947
-
Microwave irradiation for the facile synthesis of transition-metal nanoparticles (NPs) in ionic liquids (ILs) from metal-carbonyl precursors and Ru-, Rh-, Ir-NP/IL dispersions as biphasic liquid-liquid hy-drogenation nanocatalysts for cyclohexene
-
Vollmer, C.; Redel, E.; Abu-Shandi, K.; Thomann, R.; Manyar, H.; Har-dacre, C.; Janiak, C. Microwave irradiation for the facile synthesis of transition-metal nanoparticles (NPs) in ionic liquids (ILs) from metal-carbonyl precursors and Ru-, Rh-, Ir-NP/IL dispersions as biphasic liquid-liquid hy-drogenation nanocatalysts for cyclohexene. Chem. Eur. J. 2010, 16, 3849-3858.
-
(2010)
Chem. Eur. J
, vol.16
, pp. 3849-3858
-
-
Vollmer, C.1
Redel, E.2
Abu-Shandi, K.3
Thomann, R.4
Manyar, H.5
Har-Dacre, C.6
Janiak, C.7
-
134
-
-
69349103555
-
A facile synthesis of palladium nanoparticles supported on functional carbon nanotubes and its novel catalysis for ethanol electrooxidation
-
Chen, X.; Lin, Z.; Jia, T.; Cai, Z.; Huang, X.; Jiang, Y.; Chen, X.; Chen, G. A facile synthesis of palladium nanoparticles supported on functional carbon nanotubes and its novel catalysis for ethanol electrooxidation. Anal. Chim. Acta 2009, 650, 54-58.
-
(2009)
Anal. Chim. Acta
, vol.650
, pp. 54-58
-
-
Chen, X.1
Lin, Z.2
Jia, T.3
Cai, Z.4
Huang, X.5
Jiang, Y.6
Chen, X.7
Chen, G.8
-
135
-
-
33846604696
-
Grafting of palladium nanoparticles onto mesoporous molecular sieve MCM-41: Heterogeneous catalysts for the formation of an N-substituted pyrrol
-
Demel, J.; Cejka, J.; Bakardjieva, S.; Stepnicka, P. Grafting of palladium nanoparticles onto mesoporous molecular sieve MCM-41: Heterogeneous catalysts for the formation of an N-substituted pyrrol. J. Mol. Cat. A Chem. 2007, 263, 259-265.
-
(2007)
J. Mol. Cat. a Chem
, vol.263
, pp. 259-265
-
-
Demel, J.1
Cejka, J.2
Bakardjieva, S.3
Stepnicka, P.4
-
136
-
-
43149095348
-
Palladium nanoparticles stabilized by an ionic polymer and ionic liquid: A versatile system for C-C cross-coupling reactions
-
Yang, X.; Fei, Z.; Zhao, D.; Ang, W. H.; Li, Y.; Dyson, P. J. Palladium nanoparticles stabilized by an ionic polymer and ionic liquid: A versatile system for C-C cross-coupling reactions. Inorg. Chem. 2008, 47, 3292-3297.
-
(2008)
Inorg. Chem
, vol.47
, pp. 3292-3297
-
-
Yang, X.1
Fei, Z.2
Zhao, D.3
Ang, W.H.4
Li, Y.5
Dyson, P.J.6
-
137
-
-
40849119489
-
C-H activation and C-C coupling of 4-methylpyridine using palladium supported on nanoparticle alumina
-
Neal, L. M.; Hagelin-Weaver, H. E. C-H activation and C-C coupling of 4-methylpyridine using palladium supported on nanoparticle alumina. J. Mol. Catal. A Chem. 2008, 284, 141-148.
-
(2008)
J. Mol. Catal. a Chem
, vol.284
, pp. 141-148
-
-
Neal, L.M.1
Hagelin-Weaver, H.E.2
-
138
-
-
67650563869
-
Palladium nanoparticles on graphite oxide and its functionalized graphene derivatives as highly active catalysts for the Suzuki-Miyaura coupling reaction
-
Scheuermann, G. M.; Rumi, L.; Steurer, P.; Bannwarth, W.; Mülhaupt, R. Palladium nanoparticles on graphite oxide and its functionalized graphene derivatives as highly active catalysts for the Suzuki-Miyaura coupling reaction. J. Am. Chem. Soc. 2009, 131, 8262-8270.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 8262-8270
-
-
Scheuermann, G.M.1
Rumi, L.2
Steurer, P.3
Bannwarth, W.4
Mülhaupt, R.5
-
139
-
-
77950296598
-
Palladium nanoparticles supported on modified crosslinked polyacrylamide containing phophinite ligand: A novel and efficient heterogeneous catalyst for carbon-carbon cross-coupling reactions
-
Tamami, B.; Ghasemi, S. Palladium nanoparticles supported on modified crosslinked polyacrylamide containing phophinite ligand: A novel and efficient heterogeneous catalyst for carbon-carbon cross-coupling reactions. J. Mol. Catal. A Chem. 2010, 322, 98-105.
-
(2010)
J. Mol. Catal. a Chem
, vol.322
, pp. 98-105
-
-
Tamami, B.1
Ghasemi, S.2
-
140
-
-
47549103690
-
Facile synthesis of palladium nanoclusters and their catalytic activity in Sonogashira coupling reactions
-
Athilakshmi, J.; Ramanathan, S.; Chand, D. K. Facile synthesis of palladium nanoclusters and their catalytic activity in Sonogashira coupling reactions. Tetrahedron Lett. 2008, 49, 5286-5288.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 5286-5288
-
-
Athilakshmi, J.1
Ramanathan, S.2
Chand, D.K.3
-
141
-
-
77950297781
-
Pd colloid grafted mesoporous silica and its extraordinarily high catalytic activity for Mizoroki-Heck reactions
-
Feng, Y.; Li, L.; Li, Y.; Zhao, W.; Gu, J.; Shi, J. Pd colloid grafted mesoporous silica and its extraordinarily high catalytic activity for Mizoroki-Heck reactions. J. Mol. Catal. A Chem. 2010, 322, 50-54.
-
(2010)
J. Mol. Catal. a Chem
, vol.322
, pp. 50-54
-
-
Feng, Y.1
Li, L.2
Li, Y.3
Zhao, W.4
Gu, J.5
Shi, J.6
-
142
-
-
53049096670
-
Heterogeneous copper-free Sonogashira coupling reaction of terminal alkynes with aryl halides over a quinoline-2-carboimine palladium complex immobilized on MCM-41
-
Komura, K.; Nakamura, H.; Sugi, Y. Heterogeneous copper-free Sonogashira coupling reaction of terminal alkynes with aryl halides over a quinoline-2-carboimine palladium complex immobilized on MCM-41. J. Mol. Catal. A Chem. 2008, 293, 72-78.
-
(2008)
J. Mol. Catal. a Chem
, vol.293
, pp. 72-78
-
-
Komura, K.1
Nakamura, H.2
Sugi, Y.3
-
143
-
-
45449097624
-
A facile synthesis of terminal arylacetylenes via Sonogashira coupling reactions catalyzed by MCM-41-supported mer-capto palladium(0) complex
-
Xu, Y. P.; Hu, R. H.; Cai, M. Z. A facile synthesis of terminal arylacetylenes via Sonogashira coupling reactions catalyzed by MCM-41-supported mer-capto palladium(0) complex. Chin. Chem. Lett. 2008, 19, 783-787.
-
(2008)
Chin. Chem. Lett
, vol.19
, pp. 783-787
-
-
Xu, Y.P.1
Hu, R.H.2
Cai, M.Z.3
-
144
-
-
58049213793
-
The first heterogeneous carbonylative Sonogashira coupling reaction catalyzed by MCM-41-supported bidentate phosphine palladium(0) complex
-
Hao, W.; Sha, J.; Sheng, S.; Cai, M. The first heterogeneous carbonylative Sonogashira coupling reaction catalyzed by MCM-41-supported bidentate phosphine palladium(0) complex. J. Mol. Catal. A Chem. 2009, 298, 94-98.
-
(2009)
J. Mol. Catal. a Chem
, vol.298
, pp. 94-98
-
-
Hao, W.1
Sha, J.2
Sheng, S.3
Cai, M.4
-
145
-
-
67649854201
-
Heterogeneous Suzuki and Stille coupling reactions using highly efficient palladium(0) immobilized MCM-41 catalyst
-
Jana, S.; Haldar, S.; Koner, S. Heterogeneous Suzuki and Stille coupling reactions using highly efficient palladium(0) immobilized MCM-41 catalyst. Tetrahedron Lett. 2009, 50, 4820-4823.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4820-4823
-
-
Jana, S.1
Haldar, S.2
Koner, S.3
-
146
-
-
38149082507
-
Polymethyl methacrylate micro-spheres supported palladium: A new catalyst for Heck and Suzuki reactions
-
Song, D.; Yi, W.-B. Polymethyl methacrylate micro-spheres supported palladium: A new catalyst for Heck and Suzuki reactions. J. Mol. Catal. A Chem. 2008, 280, 20-23.
-
(2008)
J. Mol. Catal. a Chem
, vol.280
, pp. 20-23
-
-
Song, D.1
Yi, W.-B.2
-
147
-
-
75149163278
-
Soluble polysiloxane-supported catalysts for the Mizoroki-Heck reaction
-
Cypryk, M.; Pospiech, P.; Strzelec, K.; Wasikowska, K.; Sobczak, J. W. Soluble polysiloxane-supported catalysts for the Mizoroki-Heck reaction. J. Mol. Catal. A Chem. 2010, 319, 30-38.
-
(2010)
J. Mol. Catal. a Chem
, vol.319
, pp. 30-38
-
-
Cypryk, M.1
Pospiech, P.2
Strzelec, K.3
Wasikowska, K.4
Sobczak, J.W.5
-
148
-
-
53049084028
-
Silicaethylphophatrioxaadaman-tane - a new support for palladium catalysts and evaluation in Suzuki coupling reactions
-
Guinó, M.; Sullivan, A. C.; Wilson, J. R. H. Silicaethylphophatrioxaadaman-tane - a new support for palladium catalysts and evaluation in Suzuki coupling reactions. J. Mol. Catal. A Chem. 2008, 293, 25-30.
-
(2008)
J. Mol. Catal. a Chem
, vol.293
, pp. 25-30
-
-
Guinó, M.1
Sullivan, A.C.2
Wilson, J.R.H.3
-
149
-
-
53649110239
-
2]: A recyclable and ligand-free palladium catalyst for copper-free Sonogashira coupling reaction in water under aerobic conditions
-
Ye, Z.-W.; Yi, W.-B. Polymer-supported palladium perfluorooctanesulfonate [Pd(OPf)2]: A recyclable and ligand-free palladium catalyst for copper-free Sonogashira coupling reaction in water under aerobic conditions. J. Fluorine Chem. 2008, 129, 1124-1128.
-
(2008)
J. Fluorine Chem
, vol.129
, pp. 1124-1128
-
-
Ye, Z.-W.1
Yi, W.-B.2
-
150
-
-
77954244523
-
Chemoenzymatic synthesis of the calci-mimetics (+)-NPS R-568 via asymmetric reductive acylation of ketoxime intermediate
-
Han, K.; Kim, Y.; Park, J.; Kim, M. Chemoenzymatic synthesis of the calci-mimetics (+)-NPS R-568 via asymmetric reductive acylation of ketoxime intermediate. Tetrahedron Lett. 2010, 51, 3536-3537.
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 3536-3537
-
-
Han, K.1
Kim, Y.2
Park, J.3
Kim, M.4
-
151
-
-
72449170089
-
Transition-metal-catalyzed directed arylation of (hetero)arenes by C-H bond activation
-
For a recent review on C-H activation, see
-
For a recent review on C-H activation, see: Ackermann, L.; Vicente, R.; Kapdi, A. R. Transition-metal-catalyzed directed arylation of (hetero)arenes by C-H bond activation. Angew. Chem. Int. Ed. 2009, 48, 9792-9826.
-
(2009)
Angew. Chem. Int. Ed
, vol.48
, pp. 9792-9826
-
-
Ackermann, L.1
Vicente, R.2
Kapdi, A.R.3
-
152
-
-
77951842975
-
Triethanolamine-mediated palladium-catalyzed regioselective C-2 directed arylation of free NH-pyrroles
-
Jafarpour, F.; Rahiminejadan, S.; Hazrati, H. Triethanolamine-mediated palladium-catalyzed regioselective C-2 directed arylation of free NH-pyrroles. J. Org. Chem. 2010, 75, 3109-3112.
-
(2010)
J. Org. Chem
, vol.75
, pp. 3109-3112
-
-
Jafarpour, F.1
Rahiminejadan, S.2
Hazrati, H.3
|