-
1
-
-
0002583629
-
-
Reviews: a
-
Reviews: a) M. Murakami, Y. Ito, Top, Organomet. Ghent. 1999, 3, 97.
-
(1999)
Top, Organomet. Ghent
, vol.3
, pp. 97
-
-
Murakami, M.1
Ito, Y.2
-
6
-
-
0034679467
-
-
a) M. Murakami, T. Tsuruta, Y. Ito, Angew. Chem., Int. Ed. 2000, 39, 2484.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 2484
-
-
Murakami, M.1
Tsuruta, T.2
Ito, Y.3
-
7
-
-
0037184466
-
-
b) M. Murakami, T. Itahashi, Y. Ito, J. Am. Chem. Soc. 2002, 124, 13976.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 13976
-
-
Murakami, M.1
Itahashi, T.2
Ito, Y.3
-
8
-
-
4644359017
-
-
c) T. Matsuda, A. Fujimoto, M. Ishibashi, M. Murakami, Chem. Lett. 2004, 33, 876.
-
(2004)
Chem. Lett
, vol.33
, pp. 876
-
-
Matsuda, T.1
Fujimoto, A.2
Ishibashi, M.3
Murakami, M.4
-
9
-
-
22744439488
-
-
d) T. Matsuda, M. Makino, M. Murakami, Angew. Chem., Int. Ed. 2005, 44, 4608.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 4608
-
-
Matsuda, T.1
Makino, M.2
Murakami, M.3
-
10
-
-
23844547924
-
-
e) T. Matsuda, M. Makino, M. Murakami, Bull. Chem. Soc. Jpn. 2005, 78, 1528.
-
(2005)
Bull. Chem. Soc. Jpn
, vol.78
, pp. 1528
-
-
Matsuda, T.1
Makino, M.2
Murakami, M.3
-
11
-
-
33744548526
-
-
f) T. Matsuda, M. Shigeno, M. Murakami, Chem. Lett. 2006, 55, 288.
-
(2006)
Chem. Lett
, vol.55
, pp. 288
-
-
Matsuda, T.1
Shigeno, M.2
Murakami, M.3
-
12
-
-
33746880626
-
-
and references therein
-
g) T. Matsuda, M. Shigeno, M. Makino, M. Murakami, Org. Lett. 2006, 8, 3379, and references therein.
-
(2006)
Org. Lett
, vol.8
, pp. 3379
-
-
Matsuda, T.1
Shigeno, M.2
Makino, M.3
Murakami, M.4
-
13
-
-
18744369601
-
-
a) M. Murakami, S. Ashida, T. Matsuda, J. Am. Chem. Soc. 2005, 127, 6932.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 6932
-
-
Murakami, M.1
Ashida, S.2
Matsuda, T.3
-
14
-
-
33644559029
-
-
b) M. Murakami, S. Ashida, T. Matsuda, J. Am. Chem. Soc. 2006, 128, 2166.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 2166
-
-
Murakami, M.1
Ashida, S.2
Matsuda, T.3
-
16
-
-
7244245518
-
-
For recent examples of catalytic cleavage of four-membered carbocyclic rings, see: a
-
For recent examples of catalytic cleavage of four-membered carbocyclic rings, see: a) T. Kondo, Y. Taguchi, Y. Kaneko, M. Niimi, T. Mitsudo, Angew. Chem., Int. Ed. 2004, 43, 5369.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5369
-
-
Kondo, T.1
Taguchi, Y.2
Kaneko, Y.3
Niimi, M.4
Mitsudo, T.5
-
17
-
-
3543014941
-
-
b) T. Nishimura, Y. Nishiguchi, Y. Maeda, S. Uemura, J. Org. Chem. 2004, 69, 5342.
-
(2004)
J. Org. Chem
, vol.69
, pp. 5342
-
-
Nishimura, T.1
Nishiguchi, Y.2
Maeda, Y.3
Uemura, S.4
-
18
-
-
9144256268
-
-
c) M. Yoshida, Y. Komatsuzaki, H. Nemoto, M. Ihara, Org. Biomol. Chem. 2004, 2, 3099.
-
(2004)
Org. Biomol. Chem
, vol.2
, pp. 3099
-
-
Yoshida, M.1
Komatsuzaki, Y.2
Nemoto, H.3
Ihara, M.4
-
19
-
-
33746278459
-
-
d) P. A. Wender, N. M. Deschamps, R. Sun, Angew. Chem., Int. Ed. 2006, 45, 3957.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 3957
-
-
Wender, P.A.1
Deschamps, N.M.2
Sun, R.3
-
21
-
-
33845262844
-
-
f) Y. Yamamoto, S. Kuwabara, H. Hayashi, H. Nishiyama, Adv. Synth. Catal. 2006, 348, 2493.
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 2493
-
-
Yamamoto, Y.1
Kuwabara, S.2
Hayashi, H.3
Nishiyama, H.4
-
22
-
-
34347264611
-
-
The produced 3aa was a racemic mixture.
-
The produced 3aa was a racemic mixture.
-
-
-
-
25
-
-
84980170257
-
-
c) M. Braun, R. Dammann, D. Seebach, Chem. Ber. 1975, 108, 2368.
-
(1975)
Chem. Ber
, vol.108
, pp. 2368
-
-
Braun, M.1
Dammann, R.2
Seebach, D.3
-
28
-
-
34347207355
-
-
4OD was used, the deuterium atom was selectively introduced at the α-position (63% D) of the produced ester to confirm the formation of the rhodium enolate.
-
4OD was used, the deuterium atom was selectively introduced at the α-position (63% D) of the produced ester to confirm the formation of the rhodium enolate.
-
-
-
-
30
-
-
0000923024
-
-
Noncatalyzed ring-opening of α,α-disubstituted cyclobutanones with primary amines was reported, a L. Ghosez, R. Montaigne, A. Roussel, H. Vanlierde, P. Mollet, Tetrahedron 1971, 27, 615.
-
Noncatalyzed ring-opening of α,α-disubstituted cyclobutanones with primary amines was reported, a) L. Ghosez, R. Montaigne, A. Roussel, H. Vanlierde, P. Mollet, Tetrahedron 1971, 27, 615.
-
-
-
-
31
-
-
0038558280
-
-
b) N. N. Van, K. Chow, H. W. Moore, J. Org. Chem. 1987, 52, 1315.
-
(1987)
J. Org. Chem
, vol.52
, pp. 1315
-
-
Van, N.N.1
Chow, K.2
Moore, H.W.3
-
32
-
-
3142657150
-
-
c) G. Verniest, S. Boterberg, F. Bombeke, C. V. Stevens, N. De Kimpe, Synlett 2004, 1059.
-
(2004)
Synlett
, pp. 1059
-
-
Verniest, G.1
Boterberg, S.2
Bombeke, F.3
Stevens, C.V.4
De Kimpe, N.5
-
33
-
-
34347212259
-
-
Heating a toluene solution of 1b and 13c at 90°C in the absence of the rhodium catalyst gave no amide 14bc.
-
Heating a toluene solution of 1b and 13c at 90°C in the absence of the rhodium catalyst gave no amide 14bc.
-
-
-
|