-
1
-
-
10944248645
-
-
For recent reviews, see, e.g.: (a) Ajamian, A.; Gleason, J. L. Angew. Chem. 2004, 116, 3842.
-
(2004)
Angew. Chem.
, vol.116
, pp. 3842
-
-
Ajamian, A.1
Gleason, J.L.2
-
2
-
-
3242702454
-
-
(b) Lee, J. M.; Na, Y.; Han, H.; Chang, S. Chem. Soc. Rev. 2004, 33, 302.
-
(2004)
Chem. Soc. Rev.
, vol.33
, pp. 302
-
-
Lee, J.M.1
Na, Y.2
Han, H.3
Chang, S.4
-
4
-
-
0242595741
-
-
For recent reviews on transition-metal-assisted sequential transformations and domino processes, see, e.g.: (a) Balme, G.; Bossharth, E.; Monteiro, N. Eur. J. Org. Chem. 2003, 4101.
-
(2003)
Eur. J. Org. Chem.
, pp. 4101
-
-
Balme, G.1
Bossharth, E.2
Monteiro, N.3
-
6
-
-
7044235861
-
-
(c) Negishi, E.-I.; Copéret, C.; Ma, S.; Liou, S.-Y.; Liu, F. Chem. Rev. 1996, 96, 365.
-
(1996)
Chem. Rev.
, vol.96
, pp. 365
-
-
Negishi, E.-I.1
Copéret, C.2
Ma, S.3
Liou, S.-Y.4
Liu, F.5
-
8
-
-
0002524474
-
-
For representative Pd-catalyzed Alder-ene reactions, see, e.g.: (a) Trost, B. M. Acc. Chem. Res. 1990, 23, 34.
-
(1990)
Acc. Chem. Res.
, vol.23
, pp. 34
-
-
Trost, B.M.1
-
11
-
-
1642379331
-
-
For leading reviews on Pd-catalyzed cycloisomerizations, see, e.g.: (a) Lloyd-Jones, G. C. Org. Biomol. Chem. 2003, 215.
-
(2003)
Org. Biomol. Chem.
, pp. 215
-
-
Lloyd-Jones, G.C.1
-
12
-
-
0036522941
-
-
(b) Aubert, C.; Buisine, O.; Malacria, M. Chem. Rev. 2002, 102, 813.
-
(2002)
Chem. Rev.
, vol.102
, pp. 813
-
-
Aubert, C.1
Buisine, O.2
Malacria, M.3
-
13
-
-
20444443308
-
-
For representative examples, see, e.g.: (a) D'Souza, D. M.; Rominger, F.; Müller, T. J. J. Angew. Chem. 2005, 117, 156;
-
(2005)
Angew. Chem.
, vol.117
, pp. 156
-
-
D'Souza, D.M.1
Rominger, F.2
Müller, T.J.J.3
-
20
-
-
0000677617
-
-
(f) Müller, T. J. J.; Ansorge, M.; Aktah, D. Angew. Chem. 2000, 112, 1323;
-
(2000)
Angew. Chem.
, vol.112
, pp. 1323
-
-
Müller, T.J.J.1
Ansorge, M.2
Aktah, D.3
-
24
-
-
0032512085
-
-
The synthesis of alkynyl allyl alcohol substrates were performed according to Sajiki, H.; Hirota, K. Tetrahedron 1998, 54, 13981. The detailed protocols will be described elsewhere.
-
(1998)
Tetrahedron
, vol.54
, pp. 13981
-
-
Sajiki, H.1
Hirota, K.2
-
25
-
-
20444440888
-
-
note
-
All compounds have been fully characterized spectroscopically and by correct elemental analysis or HRMS, respectively.
-
-
-
-
26
-
-
20444506560
-
-
note
-
2Si (198.3): C 60.56, H 9.15. Found: C 60.04, H 9.02.
-
-
-
-
27
-
-
20444478850
-
-
note
-
33NOSi (295.5): C 69.09, H 11.25, N 4.74. Found: C 69.26, H 11.09, N 4.87.
-
-
-
-
28
-
-
2542458280
-
-
Tararov, V. I.; Kadyrov, R.; Riermeier, T. H.; Fischer, C.; Börner, A. Adv. Synth. Catal. 2004, 346, 561.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 561
-
-
Tararov, V.I.1
Kadyrov, R.2
Riermeier, T.H.3
Fischer, C.4
Börner, A.5
-
29
-
-
0037195705
-
-
Kitamura, M.; Lee, D.; Hayashi, S.; Tanaka, S.; Yoshimura, M. J. Org. Chem. 2002, 67, 8685.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 8685
-
-
Kitamura, M.1
Lee, D.2
Hayashi, S.3
Tanaka, S.4
Yoshimura, M.5
|