-
2
-
-
0001108788
-
-
b) G. Dyker, Angew. Chem. 1999, 111, 1808-1822;
-
(1999)
Angew. Chem
, vol.111
, pp. 1808-1822
-
-
Dyker, G.1
-
3
-
-
0033553817
-
-
Angew. Chem. Int. Ed. 1999, 38, 1698-1712;
-
(1999)
Angew. Chem. Int. Ed
, vol.38
, pp. 1698-1712
-
-
-
5
-
-
0034867872
-
-
d) C. Jia, T. Kitamura, Y. Fujiwara, Acc. Chem. Res. 2001, 34, 633-639;
-
(2001)
Acc. Chem. Res
, vol.34
, pp. 633-639
-
-
Jia, C.1
Kitamura, T.2
Fujiwara, Y.3
-
6
-
-
0036589261
-
-
e) V. Ritleng, C. Sirlin, M. Pfeffer, Chem. Rev. 2002, 102, 1731-1770;
-
(2002)
Chem. Rev
, vol.102
, pp. 1731-1770
-
-
Ritleng, V.1
Sirlin, C.2
Pfeffer, M.3
-
9
-
-
34447131678
-
-
h) C. I. Herreras, X. Yao, Z. Li, C. J. Li, Chem. Rev. 2007, 107, 2546-2562;
-
(2007)
Chem. Rev
, vol.107
, pp. 2546-2562
-
-
Herreras, C.I.1
Yao, X.2
Li, Z.3
Li, C.J.4
-
10
-
-
34248361209
-
-
i) L. C. Campeau, D. R. Stuart, K. Fagnou, Aldrichimica Acta 2007, 40, 35-41;
-
(2007)
Aldrichimica Acta
, vol.40
, pp. 35-41
-
-
Campeau, L.C.1
Stuart, D.R.2
Fagnou, K.3
-
11
-
-
40549088216
-
-
j) Y. J. Park, J. W. Park, C. H. Jun, Acc. Chem. Res. 2008, 41, 222-234;
-
(2008)
Acc. Chem. Res
, vol.41
, pp. 222-234
-
-
Park, Y.J.1
Park, J.W.2
Jun, C.H.3
-
16
-
-
0026418434
-
-
a) B. M. Trost, Science 1991, 254, 1471-1477;
-
(1991)
Science
, vol.254
, pp. 1471-1477
-
-
Trost, B.M.1
-
17
-
-
0000791854
-
-
b) B. M. Trost, Angew. Chem. 1995, 107, 285-307;
-
(1995)
Angew. Chem
, vol.107
, pp. 285-307
-
-
Trost, B.M.1
-
20
-
-
1842712344
-
-
d) M. Eissen, R. Mazur, H. G. Quebbemann, K. H. Pennemann, Helv. Chim. Acta 2004, 87, 524-535.
-
(2004)
Helv. Chim. Acta
, vol.87
, pp. 524-535
-
-
Eissen, M.1
Mazur, R.2
Quebbemann, H.G.3
Pennemann, K.H.4
-
21
-
-
0037442914
-
-
For some recent examples of coupling reactions, see: a
-
For some recent examples of coupling reactions, see: a) F. Kakiuchi, S. Kan, K. Igi, N. Chatani, S. Murai, J. Am. Chem. Soc. 2003, 125, 1698-1699;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 1698-1699
-
-
Kakiuchi, F.1
Kan, S.2
Igi, K.3
Chatani, N.4
Murai, S.5
-
22
-
-
17844400107
-
-
b) F. Kakiuchi, Y. Matsuura, S. Kan, N. Chatani, J. Am. Chem. Soc. 2005, 127, 5936-5945;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 5936-5945
-
-
Kakiuchi, F.1
Matsuura, Y.2
Kan, S.3
Chatani, N.4
-
24
-
-
58149399967
-
-
d) S. D. Yang, C. L. Sun, Z. Fang, B. J. Li, Y. Z. Li, Z. J. Shi, Angew. Chem. 2008, 120, 1495-1498;
-
(2008)
Angew. Chem
, vol.120
, pp. 1495-1498
-
-
Yang, S.D.1
Sun, C.L.2
Fang, Z.3
Li, B.J.4
Li, Y.Z.5
Shi, Z.J.6
-
25
-
-
39849083252
-
-
Angew. Chem. Int. Ed. 2008, 47, 1473-1476;
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 1473-1476
-
-
-
26
-
-
44949242600
-
-
e) D. H. Wang, M. Wasa, R. Giri, J. Q. Yu, J. Am. Chem. Soc. 2008, 130, 7190-7191;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 7190-7191
-
-
Wang, D.H.1
Wasa, M.2
Giri, R.3
Yu, J.Q.4
-
28
-
-
53349092963
-
-
g) B. F. Shi, N. Maugel, Y. H. Zhang, J. Q. Yu, Angew. Chem. 2008, 120, 4960-4964;
-
(2008)
Angew. Chem
, vol.120
, pp. 4960-4964
-
-
Shi, B.F.1
Maugel, N.2
Zhang, Y.H.3
Yu, J.Q.4
-
29
-
-
48849108176
-
-
Angew. Chem. Int. Ed. 2008, 47, 4882-4886;
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 4882-4886
-
-
-
30
-
-
43849097670
-
-
h) L. Ackermann, A. Althammer, R. Born, Tetrahedron 2008, 64, 6115-6124;
-
(2008)
Tetrahedron
, vol.64
, pp. 6115-6124
-
-
Ackermann, L.1
Althammer, A.2
Born, R.3
-
31
-
-
58449108142
-
-
i) G. Deng, L. Zhao, C. J. Li, Angew. Chem. 2008, 120, 6374-6378;
-
(2008)
Angew. Chem
, vol.120
, pp. 6374-6378
-
-
Deng, G.1
Zhao, L.2
Li, C.J.3
-
32
-
-
53549084027
-
-
Angew. Chem. Int. Ed. 2008, 47, 6278-6282;
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 6278-6282
-
-
-
33
-
-
47749125841
-
-
j) S. H. Cho, S. J. Hwang, S. Chang, J. Am. Chem. Soc. 2008, 130, 9254-9256;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 9254-9256
-
-
Cho, S.H.1
Hwang, S.J.2
Chang, S.3
-
34
-
-
54049087464
-
-
k) I. Ban, T. Sudo, T. Taniguchi, K. Itami, Org. Lett. 2008, 10, 3607-3609;
-
(2008)
Org. Lett
, vol.10
, pp. 3607-3609
-
-
Ban, I.1
Sudo, T.2
Taniguchi, T.3
Itami, K.4
-
35
-
-
54049085812
-
-
l) S. I. Kozhushkov, D. S. Yufit, L. Ackermann, Org. Lett. 2008, 10, 3409-3412.
-
(2008)
Org. Lett
, vol.10
, pp. 3409-3412
-
-
Kozhushkov, S.I.1
Yufit, D.S.2
Ackermann, L.3
-
36
-
-
33745037965
-
-
For some recent hydroalkylation reactions: a
-
For some recent hydroalkylation reactions: a) M. M. P. Grutters, C. Müller, D. Vogt, J. Am. Chem. Soc. 2006, 128, 7414-7415;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 7414-7415
-
-
Grutters, M.M.P.1
Müller, C.2
Vogt, D.3
-
37
-
-
37349118689
-
-
b) T. Nishimura, X. X. Guo, K. Ohnishi, T. Hayashi, Adv. Synth. Catal. 2007, 349, 2669-2672;
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 2669-2672
-
-
Nishimura, T.1
Guo, X.X.2
Ohnishi, K.3
Hayashi, T.4
-
38
-
-
43949108554
-
-
c) A. S. Tsai, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc. 2008, 130, 6316-6317;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 6316-6317
-
-
Tsai, A.S.1
Bergman, R.G.2
Ellman, J.A.3
-
39
-
-
43849105130
-
-
d) Y. Kuninobu, K. Kikuchi, Y. Tokunaga, Y. Nishina, K. Takai, Tetrahedron 2008, 64, 5974-5981;
-
(2008)
Tetrahedron
, vol.64
, pp. 5974-5981
-
-
Kuninobu, Y.1
Kikuchi, K.2
Tokunaga, Y.3
Nishina, Y.4
Takai, K.5
-
40
-
-
51049113186
-
-
e) B. A. McKeown, N. A. Foley, J. P. Lee, T. B. Gunnoe, Organometallics 2008, 27, 4031-4033;
-
(2008)
Organometallics
, vol.27
, pp. 4031-4033
-
-
McKeown, B.A.1
Foley, N.A.2
Lee, J.P.3
Gunnoe, T.B.4
-
41
-
-
51549113576
-
-
f) H. Harada, R. K. Thalji, R. G. Bergman, J. A. Ellman, J. Org. Chem. 2008, 73, 6772-6779.
-
(2008)
J. Org. Chem
, vol.73
, pp. 6772-6779
-
-
Harada, H.1
Thalji, R.K.2
Bergman, R.G.3
Ellman, J.A.4
-
42
-
-
53549093807
-
-
R. Martinez, R. Chevalier, S. Darses, J. P. Genet, Angew. Chem. 2006, 118, 8412-8415;
-
(2006)
Angew. Chem
, vol.118
, pp. 8412-8415
-
-
Martinez, R.1
Chevalier, R.2
Darses, S.3
Genet, J.P.4
-
43
-
-
33845743091
-
-
Angew. Chem. Int. Ed. 2006, 45, 8232-8235.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 8232-8235
-
-
-
44
-
-
0027913099
-
-
For ruthenium-catalyzed hydroarylation processes (Murai reaction) see: a) S. Murai, F. Kakiuchi, S. Sekine, Y. Tanaka, A. Kamatani, M. Sonoda, N. Chatani, Nature 1993, 366, 529-531;
-
For ruthenium-catalyzed hydroarylation processes (Murai reaction) see: a) S. Murai, F. Kakiuchi, S. Sekine, Y. Tanaka, A. Kamatani, M. Sonoda, N. Chatani, Nature 1993, 366, 529-531;
-
-
-
-
45
-
-
0001818455
-
-
b) F. Kakiuchi, S. Sekine, Y. Tanaka, A. Kamatani, M. Sonoda, N. Chatani, S. Murai, Bull. Chem. Soc. Jpn. 1995, 68, 62-83;
-
(1995)
Bull. Chem. Soc. Jpn
, vol.68
, pp. 62-83
-
-
Kakiuchi, F.1
Sekine, S.2
Tanaka, Y.3
Kamatani, A.4
Sonoda, M.5
Chatani, N.6
Murai, S.7
-
46
-
-
0000589745
-
-
c) M. Sonoda, F. Kakiuchi, N. Chatani, S. Murai, Bull. Chem. Soc. Jpn. 1997, 70, 3117-3128;
-
(1997)
Bull. Chem. Soc. Jpn
, vol.70
, pp. 3117-3128
-
-
Sonoda, M.1
Kakiuchi, F.2
Chatani, N.3
Murai, S.4
-
47
-
-
0000526624
-
-
d) S. Murai, N. Chatani, F. Kakiuchi, Pure Appl. Chem. 1997, 69, 589-594;
-
(1997)
Pure Appl. Chem
, vol.69
, pp. 589-594
-
-
Murai, S.1
Chatani, N.2
Kakiuchi, F.3
-
48
-
-
0004746026
-
-
e) N. Fujii, F. Kakiuchi, A. Yamada, N. Chatani, S. Murai, Bull. Chem. Soc. Jpn. 1998, 71, 285-298;
-
(1998)
Bull. Chem. Soc. Jpn
, vol.71
, pp. 285-298
-
-
Fujii, N.1
Kakiuchi, F.2
Yamada, A.3
Chatani, N.4
Murai, S.5
-
51
-
-
0000893516
-
-
For some examples see: a
-
For some examples see: a) F. Kakiuchi, Y. Tanaka, T. Sato, N. Chatani, S. Murai, Chem. Lett. 1995, 24, 679-680;
-
(1995)
Chem. Lett
, vol.24
, pp. 679-680
-
-
Kakiuchi, F.1
Tanaka, Y.2
Sato, T.3
Chatani, N.4
Murai, S.5
-
52
-
-
0000797948
-
-
b) B. M. Trost, K. Imi, I. W. Davies, J. Am. Chem. Soc. 1995, 117, 5371-5372;
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 5371-5372
-
-
Trost, B.M.1
Imi, K.2
Davies, I.W.3
-
53
-
-
0000179752
-
-
c) T. Sato, F. Kakiuchi, N. Chatani, S. Murai, Chem. Lett. 1998, 27, 893-894;
-
(1998)
Chem. Lett
, vol.27
, pp. 893-894
-
-
Sato, T.1
Kakiuchi, F.2
Chatani, N.3
Murai, S.4
-
54
-
-
0035533839
-
-
d) F. Kakiuchi, T. Sato, K. Igi, N. Chatani, S. Murai, Chem. Lett. 2001, 30, 386-387;
-
(2001)
Chem. Lett
, vol.30
, pp. 386-387
-
-
Kakiuchi, F.1
Sato, T.2
Igi, K.3
Chatani, N.4
Murai, S.5
-
55
-
-
0042693206
-
-
e) G. Hughes, M. Kimura, S. L. Buchwald, J. Am. Chem. Soc. 2003, 125, 11253-11258.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 11253-11258
-
-
Hughes, G.1
Kimura, M.2
Buchwald, S.L.3
-
57
-
-
84961484227
-
-
review on allylsilanes: b
-
review on allylsilanes: b) H. Sakurai, Pure Appl. Chem. 1982, 54, 1-22;
-
(1982)
Pure Appl. Chem
, vol.54
, pp. 1-22
-
-
Sakurai, H.1
-
61
-
-
35948938877
-
-
for some recent examples of the formation of allysilanes: f
-
for some recent examples of the formation of allysilanes: f) R. Shintani, Y. Ichikawa, T. Hayashi, J. Chen, Y. Nakao, T. Hiyama, Org. Lett. 2007, 9, 4643-4645;
-
(2007)
Org. Lett
, vol.9
, pp. 4643-4645
-
-
Shintani, R.1
Ichikawa, Y.2
Hayashi, T.3
Chen, J.4
Nakao, Y.5
Hiyama, T.6
-
64
-
-
0346346425
-
-
review
-
b) review: J. Singh, N. Satyamurthi, I. S. Aidhen, J. Prakt. Chem. 2000, 342, 340-347.
-
(2000)
J. Prakt. Chem
, vol.342
, pp. 340-347
-
-
Singh, J.1
Satyamurthi, N.2
Aidhen, I.S.3
-
65
-
-
58549118165
-
-
2 (25:75). On the contrary, the E/Z ratio for allylic adduct is depending on the nature of the solvent; the following E/Z ratio were obtained (reactions conducted at 90-100°C): toluene (86:14), cyclohexane (92:2), i-PrOH (97:3), dioxane (97:3).
-
2 (25:75). On the contrary, the E/Z ratio for allylic adduct is depending on the nature of the solvent; the following E/Z ratio were obtained (reactions conducted at 90-100°C): toluene (86:14), cyclohexane (92:2), i-PrOH (97:3), dioxane (97:3).
-
-
-
-
66
-
-
0012798986
-
-
a) A. Yanagisawa, H. Kageyama, Y. Nakatsuka, K. Asakawa, Y. Matsumoto, H. Yamamoto, Angew. Chem. 1999, 111, 3916-3919;
-
(1999)
Angew. Chem
, vol.111
, pp. 3916-3919
-
-
Yanagisawa, A.1
Kageyama, H.2
Nakatsuka, Y.3
Asakawa, K.4
Matsumoto, Y.5
Yamamoto, H.6
-
67
-
-
0033576661
-
-
Angew. Chem. Int. Ed. 1999, 38, 3701-3703;
-
(1999)
Angew. Chem. Int. Ed
, vol.38
, pp. 3701-3703
-
-
-
68
-
-
0038337784
-
-
see also: b
-
see also: b) M. Wadamoto, N. Ozasa, A. Yanagisawa, H. Yamamoto, J. Org. Chem. 2003, 68, 5593-5601;
-
(2003)
J. Org. Chem
, vol.68
, pp. 5593-5601
-
-
Wadamoto, M.1
Ozasa, N.2
Yanagisawa, A.3
Yamamoto, H.4
-
71
-
-
0035955158
-
-
For examples using unfunctionnalized allyltrichlorosilanes: a
-
For examples using unfunctionnalized allyltrichlorosilanes: a) S. E. Denmark, J. Fu, J. Am. Chem. Soc. 2001, 123, 9488-9489;
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 9488-9489
-
-
Denmark, S.E.1
Fu, J.2
-
72
-
-
33644532245
-
-
b) S. E. Denmark, J. Fu, M. J. Lawler, J. Org. Chem. 2006, 71, 1523-1536;
-
(2006)
J. Org. Chem
, vol.71
, pp. 1523-1536
-
-
Denmark, S.E.1
Fu, J.2
Lawler, M.J.3
-
73
-
-
33847632961
-
-
and references cited therein
-
c) S. Kotani, S. Hashimoto, M. Nakajima, Tetrahedron 2007, 63, 3122-3132 and references cited therein.
-
(2007)
Tetrahedron
, vol.63
, pp. 3122-3132
-
-
Kotani, S.1
Hashimoto, S.2
Nakajima, M.3
-
74
-
-
0032501467
-
-
a) T. Matsubara, N. Koga, D. G. Musaev, K. Morokuma, J. Am. Chem. Soc. 1998, 120, 12692-12693;
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 12692-12693
-
-
Matsubara, T.1
Koga, N.2
Musaev, D.G.3
Morokuma, K.4
-
75
-
-
0000782830
-
-
b) Y. Guari, S. Sabo-Etienne, B. Chaudret, J. Am. Chem. Soc. 1998, 120, 4228-4229;
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 4228-4229
-
-
Guari, Y.1
Sabo-Etienne, S.2
Chaudret, B.3
-
76
-
-
0033703742
-
-
c) T. Matsubara, N. Koga, D. G. Musaev, K. Morokuma, Organometallics 2000, 19, 2318-2329;
-
(2000)
Organometallics
, vol.19
, pp. 2318-2329
-
-
Matsubara, T.1
Koga, N.2
Musaev, D.G.3
Morokuma, K.4
-
77
-
-
0035921529
-
-
d) R. F. R. Jazzar, M. F. Mahon, M. K. Whittlesey, Organometallics 2001, 20, 3745-3751.
-
(2001)
Organometallics
, vol.20
, pp. 3745-3751
-
-
Jazzar, R.F.R.1
Mahon, M.F.2
Whittlesey, M.K.3
|