-
1
-
-
33645018038
-
-
For recent example, see Grotjahn, D. B.; Zeng, X.; Cooksy, A. L. J. Am. Chem. Soc. 2006, 128, 2798.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2798
-
-
Grotjahn, D.B.1
Zeng, X.2
Cooksy, A.L.3
-
8
-
-
4744342870
-
-
Mamane, V.; Hannen, P.; Fürstner, A. Chem.-Eur. J. 2004, 10, 4556.
-
(2004)
Chem.-Eur. J.
, vol.10
, pp. 4556
-
-
Mamane, V.1
Hannen, P.2
Fürstner, A.3
-
9
-
-
0013248212
-
-
Katayama, H.; Wada, C.; Taniguchi, K.; Ozawa, F. Organometallics 2002, 21, 3285.
-
(2002)
Organometallics
, vol.21
, pp. 3285
-
-
Katayama, H.1
Wada, C.2
Taniguchi, K.3
Ozawa, F.4
-
10
-
-
6444220131
-
-
Shirakawa, E.; Morita, R.; Tsuchimoto, T.; Kawakami, Y. J. Am. Chem. Soc. 2004, 126, 13614.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13614
-
-
Shirakawa, E.1
Morita, R.2
Tsuchimoto, T.3
Kawakami, Y.4
-
11
-
-
0035819945
-
-
Kel'in, A. V.; Sromek, A. W.; Gevorgyan, V. J. Am. Chem. Soc. 2001, 123, 2074.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 2074
-
-
Kel'In, A.V.1
Sromek, A.W.2
Gevorgyan, V.3
-
12
-
-
33748763533
-
-
note
-
See Supporting Information for details.
-
-
-
-
13
-
-
33748783027
-
-
note
-
9
-
-
-
-
16
-
-
0034600902
-
-
For Au-catalyzed synthesis of heterocycles, see (c) Hashmi, A. S. K.; Schwarz, L.; Choi, J.-H.; Frost, T. M. Angew. Chem., Int. Ed. 2000, 39, 2285.
-
(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 2285
-
-
Hashmi, A.S.K.1
Schwarz, L.2
Choi, J.-H.3
Frost, T.M.4
-
17
-
-
4544255270
-
-
(d) Yao, T.; Zhang, X.; Larock, R. C. J. Am. Chem. Soc. 2004, 126, 11164.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 11164
-
-
Yao, T.1
Zhang, X.2
Larock, R.C.3
-
20
-
-
23044485049
-
-
(g) Sromek, A. W.; Rubina, M.; Gevorgyan, V. J. Am. Chem. Soc. 2005, 127, 10500.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10500
-
-
Sromek, A.W.1
Rubina, M.2
Gevorgyan, V.3
-
21
-
-
23844478167
-
-
(h) Gorin, D. J.; Davis, N. R.; Toste, F. D. J. Am. Chem. Soc. 2005, 127, 11260.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 11260
-
-
Gorin, D.J.1
Davis, N.R.2
Toste, F.D.3
-
23
-
-
17744400103
-
-
(j) Shi, X.; Gorin, D. J.; Toste, F. D. J. Am. Chem. Soc. 2005, 127, 5802.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 5802
-
-
Shi, X.1
Gorin, D.J.2
Toste, F.D.3
-
24
-
-
4444291533
-
-
(k) Luzung, M. R.; Markham, J. P.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 10858.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 10858
-
-
Luzung, M.R.1
Markham, J.P.2
Toste, F.D.3
-
26
-
-
18244399612
-
-
(m) Nieto-Oberhuber, C.; Lopez, S.; Echavarren, A. M. J. Am. Chem. Soc. 2005, 127, 6178.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 6178
-
-
Nieto-Oberhuber, C.1
Lopez, S.2
Echavarren, A.M.3
-
27
-
-
0037202125
-
-
See also (n) Asao, N.; Takahashi, K.; Lee, S.; Kasahara, T.; Yamamoto, Y. J. Am. Chem. Soc. 2002, 124, 12650.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 12650
-
-
Asao, N.1
Takahashi, K.2
Lee, S.3
Kasahara, T.4
Yamamoto, Y.5
-
29
-
-
28844458694
-
-
(p) Zhang, L. J. Am. Chem. Soc. 2005, 127, 16804. See also ref 5.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 16804
-
-
Zhang, L.1
-
30
-
-
33748795776
-
-
note
-
For Au-catalyzed propargyl-allenyl prototropic isomerization, see ref 11c.
-
-
-
-
31
-
-
0005891632
-
-
Houben-Weyl E6a/2a; Thieme: New York
-
For review, see for example Behnisch, R.; Behnisch, P.; Eggenweiler, M.; Wallenhorst, T. Indolizine; In Houben-Weyl E6a/2a; Thieme: New York, 1994; p 323.
-
(1994)
Indolizine
, pp. 323
-
-
Behnisch, R.1
Behnisch, P.2
Eggenweiler, M.3
Wallenhorst, T.4
-
32
-
-
9544235161
-
-
For pharmacologically important indolizines, see, for example (a) Hagishita, S.; Yamada, M.; Shirahase, K.; Okada, T.; Murakami, Y.; Ito, Y.; Matsuura, T.; Wada, M.; Kato, T.; Ueno, M.; Chikazawa, Y.; Yamada, K.; Ono, T.; Teshirogi, I.; Ohtani, M. J. Med. Chem. 1996, 39, 3636.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3636
-
-
Hagishita, S.1
Yamada, M.2
Shirahase, K.3
Okada, T.4
Murakami, Y.5
Ito, Y.6
Matsuura, T.7
Wada, M.8
Kato, T.9
Ueno, M.10
Chikazawa, Y.11
Yamada, K.12
Ono, T.13
Teshirogi, I.14
Ohtani, M.15
-
34
-
-
0344420059
-
-
(c) Gundersen, L.-L.; Malterudb, K. E.; Negussiea, A. H.; Risea, F.; Teklua, S.; Østby, O. B. Bioorg. Med. Chem. 2003, 11, 5409.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 5409
-
-
Gundersen, L.-L.1
Malterudb, K.E.2
Negussiea, A.H.3
Risea, F.4
Teklua, S.5
Østby, O.B.6
-
35
-
-
33748796854
-
-
note
-
3 as a precatalyst, the latter can be reduced to Au(I) species via various redox processes. See ref 11b for discussion.
-
-
-
-
37
-
-
33748788763
-
-
note
-
9 For deuterium scrambling in N-unsubstituted pyrrole ring in the presence of Au(I) complexes, see ref 11h.
-
-
-
-
38
-
-
33748768172
-
-
note
-
Equal distribution of deuterium between positions C-2 and C-3 is possible via path A if there is no H/D kinetic isotope effect (transformation 6 to 4). Obviously, path B cannot explain the observed scrambling of deuterium at C-2.
-
-
-
|