-
2
-
-
13844255135
-
-
(b)B. Chen, U. Dingerdissen, J. G. E. Krauter, H. G. J. Lansink Rotgerink, K. Mo̧bus, D. J. Ostgard, P. Panster, T. H. Riermeier, S. Seebald, T. Tacke, H. Trauthwein, Appl. Catal. A 2005, 280, 17-46;
-
(2005)
Appl. Catal. A
, vol.280
, pp. 17-46
-
-
Chen, B.1
Dingerdissen, U.2
Krauter, J.G.E.3
Lansink Rotgerink, H.G.J.4
Mo̧bus, K.5
Ostgard, D.J.6
Panster, P.7
Riermeier, T.H.8
Seebald, S.9
Tacke, T.10
Trauthwein, H.11
-
3
-
-
20444382213
-
-
(c)J. W. Yang, M. T. Hechavarria Fonseca, N. Viganola, B. List, Angew. Chem. 2004, 116, 6829-6832;
-
(2004)
Angew. Chem.
, vol.116
, pp. 6829-6832
-
-
Yang, J.W.1
Hechavarria Fonseca, M.T.2
Viganola, N.3
List, B.4
-
4
-
-
10944220196
-
-
Angew. Chem. Int. Ed. 2004, 43, 6660-6662.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6660-6662
-
-
-
6
-
-
0141800091
-
-
(b) K. Everaere, A. Mortrex, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67-77.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 67-77
-
-
Everaere, K.1
Mortrex, A.2
Carpentier, J.-F.3
-
7
-
-
33845378909
-
-
(a)R. Johnstone, A. H. Wilby, I. D. Entwistle, Chem. Rev. 1985, 85, 129-170;
-
(1985)
Chem. Rev.
, vol.85
, pp. 129-170
-
-
Johnstone, R.1
Wilby, A.H.2
Entwistle, I.D.3
-
10
-
-
0041736506
-
-
(d) S. K. Mohapatra, S. U. Sonavane, R. V. Jayaram, P. Selvam, Org. Lett. 2002, 4, 4297-4300.
-
(2002)
Org. Lett.
, vol.4
, pp. 4297-4300
-
-
Mohapatra, S.K.1
Sonavane, S.U.2
Jayaram, R.V.3
Selvam, P.4
-
11
-
-
64549133435
-
-
(a)J. Zhang, P. G. Blazecka, M. M. Bruendl, Y. Huang, J. Org. Chem. 2009, 74, 1411-1414;
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1411-1414
-
-
Zhang, J.1
Blazecka, P.G.2
Bruendl, M.M.3
Huang, Y.4
-
12
-
-
0037459518
-
-
(b)J. Yu, H. Wu, C. Ramarao, J. B. Spencer, S. V. Ley, Chem. Commun. 2003, 678-679;
-
(2003)
Chem. Commun.
, pp. 678-679
-
-
Yu, J.1
Wu, H.2
Ramarao, C.3
Spencer, J.B.4
Ley, S.V.5
-
13
-
-
0034736377
-
-
(c) T. Koike, K. Murata, T. Ikariya, Org. Lett. 2000, 2, 3833-3836.
-
(2000)
Org. Lett.
, vol.2
, pp. 3833-3836
-
-
Koike, T.1
Murata, K.2
Ikariya, T.3
-
14
-
-
62749104392
-
-
(a)N. A. Cortez, G. Aguirre, M. Parra-Hake, R. Somanathan, Tetrahedron Lett. 2009, 50, 2228-2231;
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2228-2231
-
-
Cortez, N.A.1
Aguirre, G.2
Parra-Hake, M.3
Somanathan, R.4
-
15
-
-
28244454816
-
-
(b)K. Prasad, X. Jiang, J. S. Slade, J. Clemens, O. Repic, T. J. Blacklock, 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
-
16
-
-
0001210615
-
-
(c)H. Wiener, J. Blum, Y. Sasson, J. Org. Chem. 1991, 56, 4481-4486;
-
(1991)
J. Org. Chem.
, vol.56
, pp. 4481-4486
-
-
Wiener, H.1
Blum, J.2
Sasson, Y.3
-
18
-
-
1542741084
-
-
(a)M. Baidossi, A. V. Joshi, S. Mukhopadhyay, Y. Sasson, Synth. Commun. 2004, 34, 643-650;
-
(2004)
Synth. Commun.
, vol.34
, pp. 643-650
-
-
Baidossi, M.1
Joshi, A.V.2
Mukhopadhyay, S.3
Sasson, Y.4
-
19
-
-
53849132291
-
-
(b)X. F. Wu, J. K. Liu, X. H. Li, A. Zanotti-Gerosa, F. Hancock, D. Vinci, J. W. Ruan, J. L. Xiao, Angew. Chem. 2006, 118, 6870-6874;
-
(2006)
Angew. Chem.
, vol.118
, pp. 6870-6874
-
-
Wu, X.F.1
Liu, J.K.2
Li, X.H.3
Zanotti-Gerosa, A.4
Hancock, F.5
Vinci, D.6
Ruan, J.W.7
Xiao, J.L.8
-
20
-
-
33750193289
-
-
Angew. Chem. Int. Ed. 2006, 45, 6718-6722;
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6718-6722
-
-
-
21
-
-
44649202720
-
-
(c)J. Li, Y. M. Zhang, D. F. Han, J. B. Gao, L. Zhong, C. Li, Green Chem. 2008, 10, 608-611;
-
(2008)
Green Chem.
, vol.10
, pp. 608-611
-
-
Li, J.1
Zhang, Y.M.2
Han, D.F.3
Gao, J.B.4
Zhong, L.5
Li, C.6
-
22
-
-
0022162368
-
-
(d) R. Bar, L. K. Bar, Y. Sasson, J. Blum, J. Mol. Catal. 1985, 33, 161-177.
-
(1985)
J. Mol. Catal.
, vol.33
, pp. 161-177
-
-
Bar, R.1
Bar, L.K.2
Sasson, Y.3
Blum, J.4
-
23
-
-
53949102801
-
-
(a)F. Z. Su, Y. M. Liu, L. C. Wang, Y. Cao, H. Y. He, K. N. Fan, Angew. Chem. 2008, 120, 340-343;
-
(2008)
Angew. Chem.
, vol.120
, pp. 340-343
-
-
Su, F.Z.1
Liu, Y.M.2
Wang, L.C.3
Cao, Y.4
He, H.Y.5
Fan, K.N.6
-
25
-
-
70349677574
-
-
(b)H. Sun, F. Z. Su, J. Ni, Y. Cao, H. Y. He, K. N. Fan, Angew. Chem. 2009, 121, 4454-4457;
-
(2009)
Angew. Chem.
, vol.121
, pp. 4454-4457
-
-
Sun, H.1
Su, F.Z.2
Ni, J.3
Cao, Y.4
He, H.Y.5
Fan, K.N.6
-
26
-
-
70349774742
-
-
Angew. Chem. Int. Ed. 2009, 48, 4390-4393;
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 4390-4393
-
-
-
27
-
-
21644475112
-
-
(c)H. Tsunoyama, H. Sakurai, Y. Negishi, T. Tsukuda, J. Am. Chem. Soc. 2005, 127, 9374-9375;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9374-9375
-
-
Tsunoyama, H.1
Sakurai, H.2
Negishi, Y.3
Tsukuda, T.4
-
28
-
-
23744433742
-
-
(d) G. J. Rodriguez-Rivera, W. B. Kim, S. T. Evans, T. Voitl, J. A. Dumesic, J. Am. Chem. Soc. 2005, 127, 10790-10791.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10790-10791
-
-
Rodriguez-Rivera, G.J.1
Kim, W.B.2
Evans, S.T.3
Voitl, T.4
Dumesic, J.A.5
-
29
-
-
0034703746
-
-
(a)P. Claus, A. Brueckner, C. Mohr, H. Hofmeister, J. Am. Chem. Soc. 2000, 122, 11430-11439;
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11430-11439
-
-
Claus, P.1
Brueckner, A.2
Mohr, C.3
Hofmeister, H.4
-
30
-
-
0037442905
-
-
(b)C. Mohr, H. Hofmeister, J. Radnik, P. Claus, J. Am. Chem. Soc. 2003, 125, 1905-1911;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 1905-1911
-
-
Mohr, C.1
Hofmeister, H.2
Radnik, J.3
Claus, P.4
-
32
-
-
34249079388
-
-
(d) A. Corma, P. Serna, H. Garcia, J. Am. Chem. Soc. 2007, 129, 6358-6359.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 6358-6359
-
-
Corma, A.1
Serna, P.2
Garcia, H.3
-
33
-
-
47949108176
-
-
F. Z. Su, L. He, J. Ni, Y. Cao, H. Y. He, K. N. Fan, Chem. Commun. 2008, 3531-3533.
-
(2008)
Chem. Commun.
, pp. 3531-3533
-
-
Su, F.Z.1
He, L.2
Ni, J.3
Cao, Y.4
He, H.Y.5
Fan, K.N.6
-
34
-
-
0037149951
-
-
C. Milone, M. L. Tropeano, P. Gulino. R. Ingaglia, G. Neri, S. Galvagno, Chem. Commun. 2002, 868-869.
-
(2002)
Chem. Commun.
, pp. 868-869
-
-
Milone, C.1
Tropeano, M.L.2
Gulino, R.3
Ingaglia, P.4
Neri, G.5
Galvagno, S.6
-
35
-
-
33745996009
-
-
(a)B. Campo, C. Petit, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 2006, 242, 162-171;
-
(2006)
J. Catal.
, vol.242
, pp. 162-171
-
-
Campo, B.1
Petit, C.2
Volpe, M.3
Ivanova, S.4
Touroude, R.5
-
36
-
-
38649131958
-
-
(b)B. Campo, C. Petit, M. Volpe, J. Catal. 2008, 254, 71-78;
-
(2008)
J. Catal.
, vol.254
, pp. 71-78
-
-
Campo, B.1
Petit, C.2
Volpe, M.3
-
37
-
-
64549106926
-
-
(c) B. Campo, G. Santori, C. Petit, M. Volpe, Appl. Catal. A 2009, 359, 79-83.
-
(2009)
Appl. Catal. A
, vol.359
, pp. 79-83
-
-
Campo, B.1
Santori, G.2
Petit, C.3
Volpe, M.4
-
38
-
-
27744498606
-
-
(a)G. Jacobs, S. Ricote, U. M. Graham, P. M. Patterson, B. H. Davis, Catal. Today 2005, 106, 259-264;
-
(2005)
Catal. Today
, vol.106
, pp. 259-264
-
-
Jacobs, G.1
Ricote, S.2
Graham, U.M.3
Patterson, P.M.4
Davis, B.H.5
-
39
-
-
34250016626
-
-
(b) A. Karpenko, R. Leppelt, V. Plzak, J. Cai, A. Chuvilin, B. Schumacher, U. Kaiser, R. J. Behm, Top. Catal. 2007, 44, 183-198.
-
(2007)
Top. Catal.
, vol.44
, pp. 183-198
-
-
Karpenko, A.1
Leppelt, R.2
Plzak, V.3
Cai, J.4
Chuvilin, A.5
Schumacher, B.6
Kaiser, U.7
Behm, R.J.8
-
40
-
-
73249126711
-
-
note
-
The transfer reduction rate was found to depend critically on the counterion of the formates, the ionic size of which determines the hydrogen-donating ability thus the dehydrogenation efficiency of the formate salts (see Table S1 and Ref. [4d]). On the other hand, the addition of a base such as potassium acetate to HCOOH accelerated the aldehyde reduction rate (see Figure S9) further confirms that HCOO ion is essential for the reaction to proceed.
-
-
-
-
41
-
-
33746418435
-
-
(a)A. Abad, C. Almela, A. Corma, H. Garcia, Chem. Commun. 2006, 3178-3180;
-
(2006)
Chem. Commun.
, pp. 3178-3180
-
-
Abad, A.1
Almela, C.2
Corma, A.3
Garcia, H.4
-
42
-
-
70349144552
-
-
(b) M. Conte, H. Miyamura, S. Kobayashi, V. Chechik, J. Am. Chem. Soc. 2009, 131, 7189-7196.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 7189-7196
-
-
Conte, M.1
Miyamura, H.2
Kobayashi, S.3
Chechik, V.4
-
43
-
-
73249129183
-
-
note
-
Based on the GC-MS analysis, no hydrogen was generated during the process of the Au/meso-CeO2-catalyzed TH of aldehydes, which indicates that the encountered reduction was a true hydrogen transfer rather than a consecutive dehydrogenation-hydrogenation ACHTUNGTRENUNGreaction.
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