-
1
-
-
41249089313
-
-
For recent examples, see: H. Zhang, M.S. Reddy, S. Phoenix, and P. Deslongchamps Angew. Chem., Int. Ed. 47 2008 1272
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 1272
-
-
Zhang, H.1
Reddy, M.S.2
Phoenix, S.3
Deslongchamps, P.4
-
6
-
-
80053079270
-
-
H. Shi, L.-C. Fang, C.-H. Tan, L.-L. Shi, W.-B. Zhang, C.-C. Li, T.-P. Luo, and Z. Yang J. Am. Chem. Soc. 133 2011 14944
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 14944
-
-
Shi, H.1
Fang, L.-C.2
Tan, C.-H.3
Shi, L.-L.4
Zhang, W.-B.5
Li, C.-C.6
Luo, T.-P.7
Yang, Z.8
-
14
-
-
0042433039
-
-
For the catalytic asymmetric Diels-Alder reaction of quinones with an ester group, see: D.A. Evans, and J. Wu J. Am. Chem. Soc. 125 2003 10162
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 10162
-
-
Evans, D.A.1
Wu, J.2
-
15
-
-
0030566793
-
-
For the catalytic asymmetric Mukaiyama-Michael reactions of a cyclic α-alkylidene β-keto ester, see: A. Bernardi, G. Colombo, and C. Scolastico Tetrahedron Lett. 37 1996 8921 In this paper, the authors described only one example affording the product in 65% yield with 63% ee.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 8921
-
-
Bernardi, A.1
Colombo, G.2
Scolastico, C.3
-
17
-
-
0034721430
-
-
D.A. Evans, T. Rovis, M.C. Kozlowski, C.W. Downey, and J.S. Tedrow J. Am. Chem. Soc. 122 2000 9134
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 9134
-
-
Evans, D.A.1
Rovis, T.2
Kozlowski, M.C.3
Downey, C.W.4
Tedrow, J.S.5
-
18
-
-
79961011045
-
-
For the catalytic asymmetric vinylogous Mukaiyama-Michael reactions of alkylidene malonates, see: Q. Zhang, X. Xiao, L. Lin, X. Liu, and X. Feng Org. Biomol. Chem. 9 2011 5748
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 5748
-
-
Zhang, Q.1
Xiao, X.2
Lin, L.3
Liu, X.4
Feng, X.5
-
21
-
-
84859593626
-
-
For the recent use of α-alkylidene β-keto esters in asymmetric catalysis, see: C. Schotes, and A. Mezzetti ACS Catal. 2 2012 528
-
(2012)
ACS Catal.
, vol.2
, pp. 528
-
-
Schotes, C.1
Mezzetti, A.2
-
22
-
-
0342740235
-
-
Strictly speaking, the bisoxazoline-Cu(II) complex may have a distorted square-planar geometry. See: D.A. Evans, S.J. Miller, and T. Lectka J. Am. Chem. Soc. 115 1993 6460
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 6460
-
-
Evans, D.A.1
Miller, S.J.2
Lectka, T.3
-
31
-
-
76249122299
-
-
Y. Shimizu, S.-L. Shi, H. Usuda, M. Kanai, and M. Shibasaki Angew. Chem., Int. Ed. 49 2010 1103
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 1103
-
-
Shimizu, Y.1
Shi, S.-L.2
Usuda, H.3
Kanai, M.4
Shibasaki, M.5
-
32
-
-
0032540703
-
-
Selected references for the utility of N-acryloyl oxazolidin-2-one and its congeners. For 1,3-dipolar additions, see: S. Kobayashi, and M. Kawamura J. Am. Chem. Soc. 120 1998 5840
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 5840
-
-
Kobayashi, S.1
Kawamura, M.2
-
36
-
-
84873956576
-
-
K. Orimoto, H. Oyama, Y. Namera, T. Niwa, and M. Nakada Org. Lett. 15 2013 768
-
(2013)
Org. Lett.
, vol.15
, pp. 768
-
-
Orimoto, K.1
Oyama, H.2
Namera, Y.3
Niwa, T.4
Nakada, M.5
-
37
-
-
84865714663
-
-
A similar concept can be found in the use of 2-alkenoyl-pyridine-N-oxides, see: A. Livieri, M. Boiocchi, G. Desimoni, and G. Faita Chem. Eur. J. 18 2012 11662
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 11662
-
-
Livieri, A.1
Boiocchi, M.2
Desimoni, G.3
Faita, G.4
-
40
-
-
79959910065
-
-
Also for the use of α,β-unsaturated 2-acylimidazole, see: X. Xu, W.-H. Hu, and M.P. Doyle Angew. Chem., Int. Ed. 50 2011 6392
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 6392
-
-
Xu, X.1
Hu, W.-H.2
Doyle, M.P.3
-
41
-
-
71749109404
-
-
A. Sakakura, R. Kondo, Y. Matsumura, M. Akakura, and K. Ishihara J. Am. Chem. Soc. 131 2009 17762
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 17762
-
-
Sakakura, A.1
Kondo, R.2
Matsumura, Y.3
Akakura, M.4
Ishihara, K.5
-
54
-
-
0034721430
-
-
D.A. Evans, T. Rovis, M.C. Kozlowski, C.W. Downey, and J.S. Tedrow J. Am. Chem. Soc. 122 2000 9134 9142
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 9134-9142
-
-
Evans, D.A.1
Rovis, T.2
Kozlowski, M.C.3
Downey, C.W.4
Tedrow, J.S.5
-
56
-
-
0001603678
-
-
T. Harada, H. Iwai, H. Takatsuki, K. Fujita, M. Kubo, and A. Oku Org. Lett. 3 2001 2101 2103
-
(2001)
Org. Lett.
, vol.3
, pp. 2101-2103
-
-
Harada, T.1
Iwai, H.2
Takatsuki, H.3
Fujita, K.4
Kubo, M.5
Oku, A.6
-
57
-
-
0035905168
-
-
G. Desimoni, G. Faita, S. Filippone, M. Mella, M.G. Zampori, and M. Zema Tetrahedron 57 2001 10203 10212
-
(2001)
Tetrahedron
, vol.57
, pp. 10203-10212
-
-
Desimoni, G.1
Faita, G.2
Filippone, S.3
Mella, M.4
Zampori, M.G.5
Zema, M.6
-
59
-
-
0346992401
-
-
X. Wang, S. Adachi, H. Iwai, H. Takatsuki, K. Fujita, M. Kubo, A. Oku, and T. Harada J. Org. Chem. 68 2003 10046 10057
-
(2003)
J. Org. Chem.
, vol.68
, pp. 10046-10057
-
-
Wang, X.1
Adachi, S.2
Iwai, H.3
Takatsuki, H.4
Fujita, K.5
Kubo, M.6
Oku, A.7
Harada, T.8
-
62
-
-
28444465918
-
-
H.L. van Lingen, F.L. van Delft, R.P.M. Storcken, K.F.W. Hekking, A. Klaassen, J.J.M. Smits, P. Ruskowska, J. Frelek, and F.P.J.T. Rutjes Eur. J. Org. Chem. 2005 4975 4987
-
(2005)
Eur. J. Org. Chem.
, pp. 4975-4987
-
-
Van Lingen, H.L.1
Van Delft, F.L.2
Storcken, R.P.M.3
Hekking, K.F.W.4
Klaassen, A.5
Smits, J.J.M.6
Ruskowska, P.7
Frelek, J.8
Rutjes, F.P.J.T.9
-
63
-
-
21244445402
-
-
G. Desimoni, G. Faita, M. Guala, A. Laurenti, and M. Mella Chem. -Eur. J. 11 2005 3816 3824
-
(2005)
Chem. -Eur. J.
, vol.11
, pp. 3816-3824
-
-
Desimoni, G.1
Faita, G.2
Guala, M.3
Laurenti, A.4
Mella, M.5
-
67
-
-
79961011045
-
-
Q. Zhang, X. Xiao, L. Lin, X. Liu, and X. Feng Org. Biomol. Chem. 9 2011 5748
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 5748
-
-
Zhang, Q.1
Xiao, X.2
Lin, L.3
Liu, X.4
Feng, X.5
-
69
-
-
0001080981
-
-
The conditions of transformations were not optimized. S. Hanessian, A. Gomtsyan, A. Payne, Y. Herve, and S. Beaudoin J. Org. Chem. 58 1993 5032
-
(1993)
J. Org. Chem.
, vol.58
, pp. 5032
-
-
Hanessian, S.1
Gomtsyan, A.2
Payne, A.3
Herve, Y.4
Beaudoin, S.5
-
71
-
-
84879205187
-
-
E. Siirola, F.G. Mutti, B. Grischek, S.F. Hoefler, W.M.F. Fabian, G. Grogan, and W. Kroutil Adv. Synth. Catal. 355 2013 1703
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 1703
-
-
Siirola, E.1
Mutti, F.G.2
Grischek, B.3
Hoefler, S.F.4
Fabian, W.M.F.5
Grogan, G.6
Kroutil, W.7
-
73
-
-
54049095251
-
-
L.M. Bishop, J.E. Barbarow, R.G. Bergman, and D. Trauner Angew. Chem., Int. Ed. 47 2008 8100
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 8100
-
-
Bishop, L.M.1
Barbarow, J.E.2
Bergman, R.G.3
Trauner, D.4
|