-
5
-
-
77954242854
-
-
U.S. Patent 0 173 143, 2006
-
Lipian, J.-H. U.S. Patent 0 173 143, 2006; Chem. Abstr. 2006, 145, 211480.
-
(2006)
Chem. Abstr.
, vol.145
, pp. 211480
-
-
Lipian, J.-H.1
-
11
-
-
85047699269
-
-
A. Berkessel, M.R.M. Andreae, H. Schmickler, and J. Lex Angew. Chem., Int. Ed. 41 2002 4481 4484
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 4481-4484
-
-
Berkessel, A.1
Andreae, M.R.M.2
Schmickler, H.3
Lex, J.4
-
14
-
-
34249053440
-
-
N. Qafisheh, S. Mukhopadhyay, A.V. Joshi, Y. Sasson, G.-K. Chuah, and S. Jaenicke Ind. Eng. Chem. Res. 46 2007 3016 3023
-
(2007)
Ind. Eng. Chem. Res.
, vol.46
, pp. 3016-3023
-
-
Qafisheh, N.1
Mukhopadhyay, S.2
Joshi, A.V.3
Sasson, Y.4
Chuah, G.-K.5
Jaenicke, S.6
-
15
-
-
31544472614
-
-
Z. Yu, S. Yan, G. Zhang, W. He, L. Wang, Y. Li, and F. Zeng Adv. Synth. Catal. 348 2006 111 117
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 111-117
-
-
Yu, Z.1
Yan, S.2
Zhang, G.3
He, W.4
Wang, L.5
Li, Y.6
Zeng, F.7
-
18
-
-
0037175077
-
-
M.A. Aramendia, V. Borau, C. Jiménez, A. Marinas, J.M. Marinas, and F.J. Urbano J. Catal. 211 2002 556 559
-
(2002)
J. Catal.
, vol.211
, pp. 556-559
-
-
Aramendia, M.A.1
Borau, V.2
Jiménez, C.3
Marinas, A.4
Marinas, J.M.5
Urbano, F.J.6
-
29
-
-
33745018360
-
-
X. Shen, A.S. Wasmuth, J. Zhao, C. Zhu, and S.G. Nelson J. Am. Chem. Soc. 128 2006 7438 7439
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 7438-7439
-
-
Shen, X.1
Wasmuth, A.S.2
Zhao, J.3
Zhu, C.4
Nelson, S.G.5
-
31
-
-
77954244492
-
-
All of allylbenzenes 1 and propenylbenzenes 2 are known compounds. References are shown in Supplementary data
-
All of allylbenzenes 1 and propenylbenzenes 2 are known compounds. References are shown in Supplementary data.
-
-
-
-
32
-
-
77954242309
-
-
note
-
2, involvement of such a species is depicted; see Refs. 41 and 42.
-
-
-
-
33
-
-
77954244243
-
-
note
-
41,42
-
-
-
-
34
-
-
77954242325
-
-
note
-
2 to the double bond of 1. However, the substituent effects observed is not likely supported by this mechanism, because it does not lead to cationic species explicitly.
-
-
-
-
36
-
-
0037425133
-
-
T. Tsuchimoto, S. Kamiyama, R. Negoro, E. Shirakawa, and Y. Kawakami Chem. Commun. 2003 852 853
-
(2003)
Chem. Commun.
, pp. 852-853
-
-
Tsuchimoto, T.1
Kamiyama, S.2
Negoro, R.3
Shirakawa, E.4
Kawakami, Y.5
-
38
-
-
77954244928
-
-
K. Mashimo, Y. Muramatsu, S. Tai, and T. Saito Jpn. Kokai Tokkyo Koho 219 2000 643 Chem. Abstr. 2000, 133, 135121
-
(2000)
Jpn. Kokai Tokkyo Koho
, vol.219
, pp. 643
-
-
Mashimo, K.1
Muramatsu, Y.2
Tai, S.3
Saito, T.4
-
39
-
-
77954243913
-
-
note
-
Under similar conditions, α-phenylstylene also affords the corresponding indane (89% yield), suggesting that the stabilization of benzyl cation by α-phenyl or methyl group results in the cyclization as shown in Scheme 2.
-
-
-
-
40
-
-
36749003707
-
-
S. Doherty, J.G. Knight, C.H. Smyth, R.W. Harrington, and W. Clegg Organometallics 26 2007 5961 5966
-
(2007)
Organometallics
, vol.26
, pp. 5961-5966
-
-
Doherty, S.1
Knight, J.G.2
Smyth, C.H.3
Harrington, R.W.4
Clegg, W.5
-
41
-
-
70349617692
-
-
J. Wu, X. Cui, L. Chen, G. Jiang, and Y. Wu J. Am. Chem. Soc. 131 2009 13888 13889
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 13888-13889
-
-
Wu, J.1
Cui, X.2
Chen, L.3
Jiang, G.4
Wu, Y.5
|