-
1
-
-
34250810082
-
Metal-catalyzed cascade reactions
-
(Ed. : T. J. J. Müller), Springer, Berlin
-
For recent reviews, see: a) "Metal-Catalyzed Cascade Reactions": Topics in Organometallic Chemistry, Vol.19 (Ed. : T. J. J. Müller), Springer, Berlin, 2006;
-
(2006)
Topics in Organometallic Chemistry
, vol.19
-
-
-
5
-
-
53849109140
-
-
Our group's work, see: a) Y. Xiao, J. Zhang, Angew. Chem. 2008, 120, 1929-1932;
-
(2008)
Angew. Chem.
, vol.120
, pp. 1929-1932
-
-
Xiao, Y.1
Zhang, J.2
-
6
-
-
41949130150
-
-
Angew. Chem. Int. Ed. 2008, 47, 1903-1906;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 1903-1906
-
-
-
7
-
-
53849093807
-
-
b) X. Yu, H. Ren, Y. Xiao, J. Zhang, Chem. Eur. J. 2008, 14, 8481-8485;
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 8481-8485
-
-
Yu, X.1
Ren, H.2
Xiao, Y.3
Zhang, J.4
-
8
-
-
55049128546
-
-
c) L. Fan, W. Zhao, W. Jiang, J. Zhang, Chem. Eur. J. 2008, 14, 9139-9142;
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 9139-9142
-
-
Fan, L.1
Zhao, W.2
Jiang, W.3
Zhang, J.4
-
12
-
-
70349782201
-
-
Angew. Chem. Int. Ed. 2009, 48, 5505-5508.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 5505-5508
-
-
-
13
-
-
51049121927
-
-
For reviews on gold-catalyzed reactions since 2008, see: a) Z. Li, C. Brouwer. C. He, Chem. Rev. 2008. 108, 3239-3265;
-
(2008)
Chem. Rev.
, vol.108
, pp. 3239-3265
-
-
Li, Z.1
Brouwer, C.2
He, C.3
-
14
-
-
51249100498
-
-
b) A. Arcadi, Chem. Rev. 2008, 108, 3266-3325;
-
(2008)
Chem. Rev.
, vol.108
, pp. 3266-3325
-
-
Arcadi, A.1
-
16
-
-
51049105959
-
-
d) D. J. Gorin, B. D. Sherry, F. D. Toste, Chem. Rev. 2008, 108, 3351-3378;
-
(2008)
Chem. Rev.
, vol.108
, pp. 3351-3378
-
-
Gorin, D.J.1
Sherry, B.D.2
Toste, F.D.3
-
19
-
-
40949091926
-
-
g) H. C. Shen, Tetrahedron 2008, 64, 3885-3903;
-
(2008)
Tetrahedron
, vol.64
, pp. 3885-3903
-
-
Shen, H.C.1
-
21
-
-
53249152128
-
-
Angew. Chem. Int. Ed. 2008, 47, 6754-6756;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 6754-6756
-
-
-
25
-
-
53249151254
-
-
Angew. Chem. Int. Ed. 2008, 47, 2178-2181.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 2178-2181
-
-
-
26
-
-
0000396789
-
-
For examples on gold-catalyzed tandem double heterocyclizations. see: a) A. S. K. Hashmi. L. Schwarz, J.-H. Choi, T. M. Frost, Angew. Chem. 2000, 112, 2382-2385;
-
(2000)
Angew. Chem.
, vol.112
, pp. 2382-2385
-
-
Hashmi, A.S.K.1
Schwarz, L.2
Choi, J.-H.3
Frost, T.M.4
-
27
-
-
0034600902
-
-
Angew. Chem. Int. Ed. 2000, 39, 2285-2288;
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 2285-2288
-
-
-
28
-
-
22244492360
-
-
b) S. Antoniotti, E. Genin, V. Michelet, J.-P. Genêt, J. Am. Chem. Soc. 2005, 127, 9976-9977;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9976-9977
-
-
Antoniotti, S.1
Genin, E.2
Michelet, V.3
Genêt, J.-P.4
-
29
-
-
39049105773
-
-
c) G. Zhang, X. Huang, G. Li. L. Zhang, J. Am. Chem. Soc. 2008, 130, 1814-1815;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 1814-1815
-
-
Zhang, G.1
Huang, X.2
Li, G.3
Zhang, L.4
-
30
-
-
60749119748
-
-
d) J. Meng, Y. L. Zhao, C. Q. Ren, Y. Li, Z. Li, Q. Liu, Chem. Eur. J. 2009, 15, 1830-1834.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 1830-1834
-
-
Meng, J.1
Zhao, Y.L.2
Ren, C.Q.3
Li, Y.4
Li, Z.5
Liu, Q.6
-
31
-
-
34250640281
-
-
For examples of gold-catalyzed domino heterocyclization/1,2-alkyl migration, see: a) S. F. Kirsch, J. T. Binder, C. Liébert, H. Menz, Angew. Chem. 2006, 118, 6010-6013;
-
(2006)
Angew. Chem.
, vol.118
, pp. 6010-6013
-
-
Kirsch, S.F.1
Binder, J.T.2
Liébert, C.3
Menz, H.4
-
32
-
-
33748529350
-
-
Angew. Chem. Int. Ed. 2006, 45, 5878-5880;
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5878-5880
-
-
-
34
-
-
34447342869
-
-
Angew. Chem. Int. Ed. 2007, 46, 5195-5197;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 5195-5197
-
-
-
35
-
-
38649108487
-
-
c) A. S. Dudnik, A. W. Sromek, M. Rubina, J. T. Kim, A. V. Kel'in. V. Gevorgyan, J. Am. Chem. Soc. 2008, 130, 1440-1452;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 1440-1452
-
-
Dudnik, A.S.1
Sromek, A.W.2
Rubina, M.3
Kim, J.T.4
Kel'In, A.V.5
Gevorgyan, V.6
-
36
-
-
52049110849
-
-
d) X.-Z. Shu, X.-Y. Liu, K.-G. Ji, H.-Q. Xiao, Y.-M. Liang, Chem. Eur. J. 2008, 14, 5282-5289;
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 5282-5289
-
-
Shu, X.-Z.1
Liu, X.-Y.2
Ji, K.-G.3
Xiao, H.-Q.4
Liang, Y.-M.5
-
38
-
-
42049119869
-
-
For recent reviews of furan synthesis, see: a) X. L. Hou, Z. Yang, K.-S. Y, H. N. C. Wong, Prog. Heterocycl. Chem. 2008, 19, 176;
-
(2008)
Prog. Heterocycl. Chem.
, vol.19
, pp. 176
-
-
Hou, X.L.1
Yang, Z.2
Y, K.-S.3
Wong, H.N.C.4
-
39
-
-
0036074242
-
-
b) A. Jeevanandam, A. Ghule, Y.-C. Ling, Curr. Org. Chem. 2002, 6, 841;
-
(2002)
Curr. Org. Chem.
, vol.6
, pp. 841
-
-
Jeevanandam, A.1
Ghule, A.2
Ling, Y.-C.3
-
45
-
-
45249087881
-
-
g) G. Balme, D. Bouyssi, N. Monteiro, Heterocyclics 2007, 73, 87-124.
-
(2007)
Heterocyclics
, vol.73
, pp. 87-124
-
-
Balme, G.1
Bouyssi, D.2
Monteiro, N.3
-
46
-
-
75649087451
-
-
For recent reviews on azepine synthesis, see: a) J. B. Bremner, Heterocycl. Chem. 2005, 17, 389;
-
(2005)
Heterocycl. Chem.
, vol.17
, pp. 389
-
-
Bremner, J.B.1
-
48
-
-
75649106900
-
-
c) J.-C. Quirion, E. Leclerc, P. Jubault, Sci. Synth. 2007, 33, 659;
-
(2007)
Sci. Synth.
, vol.33
, pp. 659
-
-
Quirion, J.-C.1
Leclerc, E.2
Jubault, P.3
-
51
-
-
4544255270
-
-
a) T. Yao, X. Zhang, R. C. Larock, J. Am. Chem. Soc. 2004, 126, 11164-11165;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 11164-11165
-
-
Yao, T.1
Zhang, X.2
Larock, R.C.3
-
54
-
-
75649108259
-
-
CCDC-736346 (5aa), CCDC-725115 (5ba), CCDC-748437 (7ab), CCDC-732510 (9) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC-736346 (5aa), CCDC-725115 (5ba), CCDC-748437 (7ab), CCDC-732510 (9) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
-
-
-
-
55
-
-
75649136639
-
-
We acknowledge one reviewer's suggestion to run 2D NMR spectra, which led us to find the different reaction pathway between imines 2 and 7.
-
We acknowledge one reviewer's suggestion to run 2D NMR spectra, which led us to find the different reaction pathway between imines 2 and 7.
-
-
-
|