-
9
-
-
70349386397
-
-
M.A.P. Martins, C.P. Frizzo, D.N. Moreira, L. Buriol, and P. Machado Chem. Rev. 109 2009 4140 4182
-
(2009)
Chem. Rev.
, vol.109
, pp. 4140-4182
-
-
Martins, M.A.P.1
Frizzo, C.P.2
Moreira, D.N.3
Buriol, L.4
MacHado, P.5
-
16
-
-
0242439345
-
-
D.A. Conlon, B. Pipik, S. Ferdinand, C.R. LeBlond, J.R. Sowa Jr., B. Izzo, P. Collins, G.-J. Ho, J.M. Williams, Y.-J. Shi, and Y. Sun Adv. Synth. Catal. 345 2003 931 935
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 931-935
-
-
Conlon, D.A.1
Pipik, B.2
Ferdinand, S.3
Leblond, C.R.4
Sowa, Jr.J.R.5
Izzo, B.6
Collins, P.7
Ho, G.-J.8
Williams, J.M.9
Shi, Y.-J.10
Sun, Y.11
-
18
-
-
0242291925
-
-
A. Arcadi, G. Cerichelli, M. Chiarini, M. Correa, and D. Zorzan Eur. J. Org. Chem. 2003 4080 4086
-
(2003)
Eur. J. Org. Chem.
, pp. 4080-4086
-
-
Arcadi, A.1
Cerichelli, G.2
Chiarini, M.3
Correa, M.4
Zorzan, D.5
-
20
-
-
14744288127
-
-
G. Cravotto, M. Beggiato, A. Penoni, G. Palmisano, S. Tollari, J.-M. Lévêque, and W. Bonrath Tetrahedron Lett. 46 2005 2267 2271
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 2267-2271
-
-
Cravotto, G.1
Beggiato, M.2
Penoni, A.3
Palmisano, G.4
Tollari, S.5
Lévêque, J.-M.6
Bonrath, W.7
-
23
-
-
70349427138
-
-
N. Batail, A. Bendjeriou, T. Lomberget, R. Barret, V. Dufaud, and L. Djakovitch Adv. Synth. Catal. 351 2009 2055 2062
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 2055-2062
-
-
Batail, N.1
Bendjeriou, A.2
Lomberget, T.3
Barret, R.4
Dufaud, V.5
Djakovitch, L.6
-
24
-
-
58449097709
-
-
H. Sajiki, T. Kurita, A. Kozaki, G. Zhang, Y. Kitamura, T. Maegawa, and K. Hirota J. Chem. Res. 2004 593 595
-
(2004)
J. Chem. Res.
, pp. 593-595
-
-
Sajiki, H.1
Kurita, T.2
Kozaki, A.3
Zhang, G.4
Kitamura, Y.5
Maegawa, T.6
Hirota, K.7
-
25
-
-
80053611709
-
-
Erratum
-
Erratum: J. Chem. Res. 2005 344
-
(2005)
J. Chem. Res.
, pp. 344
-
-
-
26
-
-
26844479323
-
-
H. Sajiki, T. Kurita, A. Kozaki, G. Zhang, Y. Kitamura, T. Maegawa, and K. Hirota Synthesis 2005 537 542
-
(2005)
Synthesis
, pp. 537-542
-
-
Sajiki, H.1
Kurita, T.2
Kozaki, A.3
Zhang, G.4
Kitamura, Y.5
Maegawa, T.6
Hirota, K.7
-
27
-
-
80053577435
-
-
Erratum
-
Erratum: Synthesis 2005 852
-
(2005)
Synthesis
, pp. 852
-
-
-
28
-
-
34547230604
-
-
T. Maegawa, Y. Kitamura, S. Sako, T. Udzu, A. Sakurai, A. Tanaka, Y. Kobayashi, K. Endo, U. Bora, T. Kurita, A. Kozaki, Y. Monguchi, and H. Sajiki Chem. - Eur. J. 13 2007 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
-
29
-
-
34548501320
-
-
Y. Kitamura, A. Sakurai, T. Udzu, T. Maegawa, Y. Monguchi, and H. Sajiki Tetrahedron 63 2007 10596 10602
-
(2007)
Tetrahedron
, vol.63
, pp. 10596-10602
-
-
Kitamura, Y.1
Sakurai, A.2
Udzu, T.3
Maegawa, T.4
Monguchi, Y.5
Sajiki, H.6
-
30
-
-
36649019339
-
-
Y. Kitamura, S. Sako, T. Udzu, A. Tsutsui, T. Maegawa, Y. Monguchi, and H. Sajiki Chem. Commun. 2007 5069 5071
-
(2007)
Chem. Commun.
, pp. 5069-5071
-
-
Kitamura, Y.1
Sako, S.2
Udzu, T.3
Tsutsui, A.4
Maegawa, T.5
Monguchi, Y.6
Sajiki, H.7
-
31
-
-
77949869499
-
-
Y. Kitamura, S. Sako, A. Tsutsui, Y. Monguchi, T. Maegawa, Y. Kitade, and H. Sajiki Adv. Synth. Catal. 352 2010 718 730
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 718-730
-
-
Kitamura, Y.1
Sako, S.2
Tsutsui, A.3
Monguchi, Y.4
Maegawa, T.5
Kitade, Y.6
Sajiki, H.7
-
32
-
-
33846873142
-
-
H. Sajiki, G. Zhang, Y. Kitamura, T. Maegawa, and K. Hirota Synlett 2005 619 622
-
(2005)
Synlett
, pp. 619-622
-
-
Sajiki, H.1
Zhang, G.2
Kitamura, Y.3
Maegawa, T.4
Hirota, K.5
-
33
-
-
80053578355
-
-
Erratum
-
Erratum: Synlett 2005 1046
-
(2005)
Synlett
, pp. 1046
-
-
-
34
-
-
53849112664
-
-
S. Mori, T. Yanase, S. Aoyagi, Y. Monguchi, T. Maegawa, and H. Sajiki Chem. - Eur. J. 14 2008 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
-
35
-
-
56749176901
-
-
Y. Monguchi, K. Kitamoto, T. Ikawa, T. Maegawa, and H. Sajiki Adv. Synth. Catal. 350 2008 2767 2777
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2767-2777
-
-
Monguchi, Y.1
Kitamoto, K.2
Ikawa, T.3
Maegawa, T.4
Sajiki, H.5
-
41
-
-
33750418419
-
-
C. Li, Q. Xin, Elsevier Amsterdam
-
T. Kitamura, T. Harada, and T. Osawa C. Li, Q. Xin, Spillover and Migration of Surface Species on Catalysts 1997 Elsevier Amsterdam 491 498
-
(1997)
Spillover and Migration of Surface Species on Catalysts
, pp. 491-498
-
-
Kitamura, T.1
Harada, T.2
Osawa, T.3
-
43
-
-
18744420034
-
-
T. Nozoe, K. Tanimoto, T. Takemitsu, T. Kitamura, T. Harada, T. Osawa, and O. Takayasu Solid State Ionics 141-142 2001 695 700
-
(2001)
Solid State Ionics
, vol.141-142
, pp. 695-700
-
-
Nozoe, T.1
Tanimoto, K.2
Takemitsu, T.3
Kitamura, T.4
Harada, T.5
Osawa, T.6
Takayasu, O.7
-
45
-
-
0001764898
-
-
S. Hermans, R. Raja, J.M. Thomas, B.F.G. Johnson, G. Sankar, and D. Gleeson Angew. Chem. 113 2001 1251 1255
-
(2001)
Angew. Chem.
, vol.113
, pp. 1251-1255
-
-
Hermans, S.1
Raja, R.2
Thomas, J.M.3
Johnson, B.F.G.4
Sankar, G.5
Gleeson, D.6
-
47
-
-
53949106420
-
-
R.D. Adams, E.M. Boswell, B. Captain, A.B. Hungria, P.A. Midgley, R. Raja, and J.M. Thomas Angew. Chem. 119 2007 8330 8333
-
(2007)
Angew. Chem.
, vol.119
, pp. 8330-8333
-
-
Adams, R.D.1
Boswell, E.M.2
Captain, B.3
Hungria, A.B.4
Midgley, P.A.5
Raja, R.6
Thomas, J.M.7
-
51
-
-
77953308470
-
-
Z. Sun, Y. Zhao, Y. Xie, R. Tao, H. Zhang, C. Huang, and Z. Liu Green Chem. 12 2010 1007 1011
-
(2010)
Green Chem.
, vol.12
, pp. 1007-1011
-
-
Sun, Z.1
Zhao, Y.2
Xie, Y.3
Tao, R.4
Zhang, H.5
Huang, C.6
Liu, Z.7
-
52
-
-
69949102994
-
-
M. Crespo-Quesada, M. Grasemann, N. Semagina, A. Renken, and L. Kiwi-Minsker Catal. Today 147 2009 247 254
-
(2009)
Catal. Today
, vol.147
, pp. 247-254
-
-
Crespo-Quesada, M.1
Grasemann, M.2
Semagina, N.3
Renken, A.4
Kiwi-Minsker, L.5
-
55
-
-
0039591719
-
-
G.W. Kalbalka, R.M. Pagni, L. Wang, V. Namboodiri, and C.M. Hair Green Chem. 2 2000 120 122
-
(2000)
Green Chem.
, vol.2
, pp. 120-122
-
-
Kalbalka, G.W.1
Pagni, R.M.2
Wang, L.3
Namboodiri, V.4
Hair, C.M.5
-
57
-
-
67650496986
-
-
P. Saha, S. Naskar, P. Paira, A. Hazra, K.B. Sahu, R. Paira, S. Banerjee, and N.B. Mondal Green Chem. 11 2009 931 934
-
(2009)
Green Chem.
, vol.11
, pp. 931-934
-
-
Saha, P.1
Naskar, S.2
Paira, P.3
Hazra, A.4
Sahu, K.B.5
Paira, R.6
Banerjee, S.7
Mondal, N.B.8
-
61
-
-
70449387280
-
-
F. Schneider, T. Szuppa, A. Stolle, B. Ondruschka, and H. Hopf Green Chem. 11 2009 1894 1899
-
(2009)
Green Chem.
, vol.11
, pp. 1894-1899
-
-
Schneider, F.1
Szuppa, T.2
Stolle, A.3
Ondruschka, B.4
Hopf, H.5
-
64
-
-
58449124884
-
-
The palladium species of 5% Pd/HP20 are supported on a polystyrene-polyvinylbenzene-based synthetic adsorbents, DIAION HP20, which is commercially available from Mitsubishi Chemical Corporation
-
The palladium species of 5% Pd/HP20 are supported on a polystyrene-polyvinylbenzene-based synthetic adsorbents, DIAION HP20, which is commercially available from Mitsubishi Chemical Corporation Y. Monguchi, Y. Fujita, K. Endo, S. Takao, M. Yoshimura, Y. Takagi, T. Maegawa, and H. Sajiki Chem. - Eur. J. 15 2009 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
-
65
-
-
0003053685
-
-
3 (Aldrich), 2.8 wt %] was used with quinoline (0.4 equiv) according to the literature, see On the other hand, over-reduction took place, i.e., diphenylethane (2%) formed together with desired cis-stilbene (35%) and trans-stilbene (3%), although the reaction was only slightly promoted to recover the staring diphenylacetylene (60%). The selective semi-hydrogenation to stilbene under the solvent-free conditions seems difficult to achieve
-
3 (Aldrich), 2.8 wt %] was used with quinoline (0.4 equiv) according to the literature, see H. Lindlar, and R. Dubis Org. Synth. 46 1966 89 92 On the other hand, over-reduction took place, i.e., diphenylethane (2%) formed together with desired cis-stilbene (35%) and trans-stilbene (3%), although the reaction was only slightly promoted to recover the staring diphenylacetylene (60%). The selective semi-hydrogenation to stilbene under the solvent-free conditions seems difficult to achieve
-
(1966)
Org. Synth.
, vol.46
, pp. 89-92
-
-
Lindlar, H.1
Dubis, R.2
-
67
-
-
33745631204
-
-
Y. Monguchi, A. Kume, K. Hattori, T. Maegawa, and H. Sajiki Tetrahedron 62 2006 7926 7933
-
(2006)
Tetrahedron
, vol.62
, pp. 7926-7933
-
-
Monguchi, Y.1
Kume, A.2
Hattori, K.3
Maegawa, T.4
Sajiki, H.5
-
68
-
-
0023024557
-
-
The melting points of the substrates and products, both of which are solid under the reaction conditions in Table 2, are as follows. 4-Azidobenzophenone (entry 6): 73-74 °C, see
-
The melting points of the substrates and products, both of which are solid under the reaction conditions in Table 2, are as follows. 4-Azidobenzophenone (entry 6): 73-74 °C, see Y. Ohba, S. Kubo, M. Nakai, A. Nagai, and M. Yoshimoto Bull. Chem. Soc. Jpn. 59 1986 2317 2320
-
(1986)
Bull. Chem. Soc. Jpn.
, vol.59
, pp. 2317-2320
-
-
Ohba, Y.1
Kubo, S.2
Nakai, M.3
Nagai, A.4
Yoshimoto, M.5
-
69
-
-
28044472221
-
-
4-Aminobenzophenone (entry 6): 122-124 °C, see
-
4-Aminobenzophenone (entry 6): 122-124 °C, see M. Gopalakrishnan, P. Sureshkumar, V. Kanagarajan, and J. Thanusu Catal. Commun. 6 2005 753 756
-
(2005)
Catal. Commun.
, vol.6
, pp. 753-756
-
-
Gopalakrishnan, M.1
Sureshkumar, P.2
Kanagarajan, V.3
Thanusu, J.4
-
70
-
-
0041050987
-
-
4-Chlorobenzoic acid (entry 13): 238 °C, see
-
4-Chlorobenzoic acid (entry 13): 238 °C, see P. Truitt, R. Stead, L.M. Long, and W.J. Middleton J. Am. Chem. Soc. 71 1949 3511 3513
-
(1949)
J. Am. Chem. Soc.
, vol.71
, pp. 3511-3513
-
-
Truitt, P.1
Stead, R.2
Long, L.M.3
Middleton, W.J.4
-
71
-
-
4444248577
-
-
Benzoic acid (entry 13): 121 °C, see
-
Benzoic acid (entry 13): 121 °C, see R.H. Eastman, and F.L. Detert J. Am. Chem. Soc. 73 1951 4511 4515
-
(1951)
J. Am. Chem. Soc.
, vol.73
, pp. 4511-4515
-
-
Eastman, R.H.1
Detert, F.L.2
-
76
-
-
33846444937
-
-
C.V. Ramana, B.K.K. Reddy, C.N. Reddy, R.G. Gonnade, and M.K. Gurjar Synlett 2007 127 128
-
(2007)
Synlett
, pp. 127-128
-
-
Ramana, C.V.1
Reddy, B.K.K.2
Reddy, C.N.3
Gonnade, R.G.4
Gurjar, M.K.5
-
77
-
-
77952850625
-
-
N. Hoshiya, M. Shimoda, H. Yoshikawa, Y. Yamashita, S. Shuto, and M. Arisawa J. Am. Chem. Soc. 132 2010 7270 7272
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 7270-7272
-
-
Hoshiya, N.1
Shimoda, M.2
Yoshikawa, H.3
Yamashita, Y.4
Shuto, S.5
Arisawa, M.6
-
80
-
-
11844305592
-
-
G.F. Manbeck, A.J. Lipman, R.A. Stockland, A.L. Freidl, A.F. Hasler, J.J. Stone, and I.A. Guzei J. Org. Chem. 70 2005 244 250
-
(2005)
J. Org. Chem.
, vol.70
, pp. 244-250
-
-
Manbeck, G.F.1
Lipman, A.J.2
Stockland, R.A.3
Freidl, A.L.4
Hasler, A.F.5
Stone, J.J.6
Guzei, I.A.7
-
82
-
-
56649116045
-
-
M.L. Kantam, R. Chakravarti, V.R. Chintareddy, B. Sreedhar, and S. Bhargava Adv. Synth. Catal. 350 2008 2544 2550
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2544-2550
-
-
Kantam, M.L.1
Chakravarti, R.2
Chintareddy, V.R.3
Sreedhar, B.4
Bhargava, S.5
-
83
-
-
62549160059
-
-
J. Mao, Q. Hua, G. Xie, J. Guo, Z. Yao, D. Shi, and S. Ji Adv. Synth. Catal. 351 2009 635 641
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 635-641
-
-
Mao, J.1
Hua, Q.2
Xie, G.3
Guo, J.4
Yao, Z.5
Shi, D.6
Ji, S.7
-
85
-
-
64549133437
-
-
T.M. Razler, Y. Hsiao, F. Qian, R. Fu, R.K. Khan, and W. Doubleday J. Org. Chem. 74 2009 1381 1384
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1381-1384
-
-
Razler, T.M.1
Hsiao, Y.2
Qian, F.3
Fu, R.4
Khan, R.K.5
Doubleday, W.6
-
86
-
-
31144451841
-
-
R. Cella, R.L.O.R. Cunha, A.E.S. Reis, D.C. Pimenta, C.F. Klitzke, and H.A. Stefani J. Org. Chem. 71 2006 244 250
-
(2006)
J. Org. Chem.
, vol.71
, pp. 244-250
-
-
Cella, R.1
Cunha, R.L.O.R.2
Reis, A.E.S.3
Pimenta, D.C.4
Klitzke, C.F.5
Stefani, H.A.6
-
87
-
-
42249099968
-
-
G.M. Allan, N. Vicker, H.R. Lawrence, H.J. Tutill, J.M. Day, M. Huchet, E. Ferrandis, M.J. Reed, A. Purohit, and B.V.L. Potter Bioorg. Med. Chem. 16 2008 4438 4456
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 4438-4456
-
-
Allan, G.M.1
Vicker, N.2
Lawrence, H.R.3
Tutill, H.J.4
Day, J.M.5
Huchet, M.6
Ferrandis, E.7
Reed, M.J.8
Purohit, A.9
Potter, B.V.L.10
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