-
2
-
-
37749043765
-
-
Organic Synthesis in Water; Grieco, P. A., Ed.; Blackie Academic and Professional: London, 1998.
-
(b) Organic Synthesis in Water; Grieco, P. A., Ed.; Blackie Academic and Professional: London, 1998.
-
-
-
-
3
-
-
0000677232
-
-
(c) Li, C.-J. Chem. Rev. 1993, 93, 2023.
-
(1993)
Chem. Rev
, vol.93
, pp. 2023
-
-
Li, C.-J.1
-
4
-
-
24044470646
-
-
(d) Li, C.-J. Chem. Rev. 2005, 105, 3095.
-
(2005)
Chem. Rev
, vol.105
, pp. 3095
-
-
Li, C.-J.1
-
10
-
-
0142196832
-
-
For theoretical studies, see: b
-
For theoretical studies, see: (b) Domingo, L. R.; Andrés, J. J. Org. Chem. 2003, 68, 8662.
-
(2003)
J. Org. Chem
, vol.68
, pp. 8662
-
-
Domingo, L.R.1
Andrés, J.2
-
11
-
-
33847014542
-
-
(c) Gordillo, R.; Dudding, T.; Anderson, C. D.; Houk, K. N. Org. Lett. 2007, 9, 501.
-
(2007)
Org. Lett
, vol.9
, pp. 501
-
-
Gordillo, R.1
Dudding, T.2
Anderson, C.D.3
Houk, K.N.4
-
12
-
-
0242432417
-
-
This reaction system was elegantly applied to asymmetric synthesis, see: (a) Huang, Y, Unni, A. K, Thadani, A. N, Rawal, V. H. Nature (London) 2003, 424, 146
-
This reaction system was elegantly applied to asymmetric synthesis, see: (a) Huang, Y.; Unni, A. K.; Thadani, A. N.; Rawal, V. H. Nature (London) 2003, 424, 146.
-
-
-
-
13
-
-
1942471019
-
-
(b) Thadani, A. N.; Stankovic, A. R.; Rawal, V. H. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 5846.
-
(2004)
Proc. Natl. Acad. Sci. U.S.A
, vol.101
, pp. 5846
-
-
Thadani, A.N.1
Stankovic, A.R.2
Rawal, V.H.3
-
14
-
-
13444265956
-
-
(c) Unni, A. K.; Takenaka, N.; Yamamoto, H.; Rawal, V. H. J. Am. Chem. Soc. 2005, 127, 1336.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 1336
-
-
Unni, A.K.1
Takenaka, N.2
Yamamoto, H.3
Rawal, V.H.4
-
15
-
-
33645537390
-
-
(d) Zhang, X.; Du, H.; Wang, Z.; Wu, Y.-D.; Ding, K. J. Org. Chem. 2006, 71, 2862.
-
(2006)
J. Org. Chem
, vol.71
, pp. 2862
-
-
Zhang, X.1
Du, H.2
Wang, Z.3
Wu, Y.-D.4
Ding, K.5
-
16
-
-
0032937199
-
-
For an example of Brønsted acid catalyzed Michael addition reactions, see
-
For an example of Brønsted acid catalyzed Michael addition reactions, see: Kotsuki, H.; Arimura, K.; Ohishi, T.; Maruzasa, R. J. Org. Chem. 1999, 64, 3770.
-
(1999)
J. Org. Chem
, vol.64
, pp. 3770
-
-
Kotsuki, H.1
Arimura, K.2
Ohishi, T.3
Maruzasa, R.4
-
17
-
-
4043154104
-
-
Recent examples of chiral organocatalyst-promoted Michael addition reactions, see: a
-
Recent examples of chiral organocatalyst-promoted Michael addition reactions, see: (a) Li, H.; Wang, Y.; Tang, L.; Deng, L. J. Am. Chem. Soc. 2004, 126, 9906.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 9906
-
-
Li, H.1
Wang, Y.2
Tang, L.3
Deng, L.4
-
18
-
-
11844302258
-
-
(b) Okino, T.; Hoashi, Y.; Furakawa, T.; Xu, X.; Takemoto, Y. J. Am. Chem. Soc. 2005, 127, 119.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 119
-
-
Okino, T.1
Hoashi, Y.2
Furakawa, T.3
Xu, X.4
Takemoto, Y.5
-
19
-
-
27144522622
-
-
(c) Wang, J.; Li, H.; Duan, W.; Zu, L.; Wang, W. Org. Lett. 2005, 7, 4713.
-
(2005)
Org. Lett
, vol.7
, pp. 4713
-
-
Wang, J.1
Li, H.2
Duan, W.3
Zu, L.4
Wang, W.5
-
21
-
-
0242408232
-
-
For a catalyst-free Michael addition reaction of α-nitro- cycloalkanones in water, see
-
For a catalyst-free Michael addition reaction of α-nitro- cycloalkanones in water, see: Miranda, S.; López-Alvarado, P.; Giorgi, G.; Rodriguez, J.; Avendaño, C.; Menéndez, J. C. Synlett 2003, 2159.
-
(2003)
Synlett
, pp. 2159
-
-
Miranda, S.1
López-Alvarado, P.2
Giorgi, G.3
Rodriguez, J.4
Avendaño, C.5
Menéndez, J.C.6
-
22
-
-
0029932703
-
-
For recent examples of metal- or base-catalyzed Michael addition reactions in water, see: a
-
For recent examples of metal- or base-catalyzed Michael addition reactions in water, see: (a) Keller, E.; Feringa, B. L. Tetrahedron Lett. 1996, 37, 1879.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 1879
-
-
Keller, E.1
Feringa, B.L.2
-
23
-
-
0034701460
-
-
(b) Mori, Y.; Kakumoto, K.; Manabe, K.; Kobayashi, S. Tetrahedron Lett. 2000, 41, 3107.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 3107
-
-
Mori, Y.1
Kakumoto, K.2
Manabe, K.3
Kobayashi, S.4
-
25
-
-
0035032716
-
-
(d) Bensa, D.; Brunei, J.-M.; Buono, G.; Rodriguez, J. Synlett 2001, 715.
-
(2001)
Synlett
, pp. 715
-
-
Bensa, D.1
Brunei, J.-M.2
Buono, G.3
Rodriguez, J.4
-
27
-
-
34250695909
-
-
(f) Aplander, K.; Ding, R.; Lindström, U. M.; Wennerberg, J.; Schultz, S. Angew. Chem. Int. Ed. 2007, 46, 4543.
-
(2007)
Angew. Chem. Int. Ed
, vol.46
, pp. 4543
-
-
Aplander, K.1
Ding, R.2
Lindström, U.M.3
Wennerberg, J.4
Schultz, S.5
-
28
-
-
0001653096
-
-
Hydrogen-bonding activation by water in Diels-Alder reaction, see: a
-
Hydrogen-bonding activation by water in Diels-Alder reaction, see: (a) Blake, J. F.; Jorgensen, W. L. J. Am. Chem. Soc. 1991, 113, 7430.
-
(1991)
J. Am. Chem. Soc
, vol.113
, pp. 7430
-
-
Blake, J.F.1
Jorgensen, W.L.2
-
29
-
-
0000886146
-
-
(b) Blake, J. F.; Lim, D.; Jorgensen, W. L. J. Org. Chem. 1994, 59, 803.
-
(1994)
J. Org. Chem
, vol.59
, pp. 803
-
-
Blake, J.F.1
Lim, D.2
Jorgensen, W.L.3
-
30
-
-
5644247697
-
-
Pihko et al. also reported about progress of the reaction between β-ketoester and azodicarboxylate without catalyst in alcohol, see
-
Pihko et al. also reported about progress of the reaction between β-ketoester and azodicarboxylate without catalyst in alcohol, see: Pihko, P. M.; Pohjakallio, A. Synlett 2004, 2115.
-
(2004)
Synlett
, pp. 2115
-
-
Pihko, P.M.1
Pohjakallio, A.2
-
31
-
-
34247228673
-
-
For recent examples of metal-catalyzed hydroxymethylation of active methylene compounds, see: a
-
For recent examples of metal-catalyzed hydroxymethylation of active methylene compounds, see: (a) Ogawa, C.; Kobayashi, S. Chem. Lett. 2007, 36, 56.
-
(2007)
Chem. Lett
, vol.36
, pp. 56
-
-
Ogawa, C.1
Kobayashi, S.2
-
32
-
-
34547210299
-
-
(b) Fukuchi, I.; Hamashima, Y.; Sodeoka, M. Adv. Synth. Catal. 2007, 349, 509.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 509
-
-
Fukuchi, I.1
Hamashima, Y.2
Sodeoka, M.3
-
34
-
-
5344224096
-
-
For reviews for dual activation, see: a
-
For reviews for dual activation, see: (a) Ma, J.-A.; Cahard, D. Angew. Chem. Int. Ed. 2004, 43, 4566.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 4566
-
-
Ma, J.-A.1
Cahard, D.2
-
35
-
-
33646069329
-
-
(b) Shibasaki, M.; Kanai, M.; Matsunaga, S. Aldrichimica Acta 2006, 39, 31.
-
(2006)
Aldrichimica Acta
, vol.39
, pp. 31
-
-
Shibasaki, M.1
Kanai, M.2
Matsunaga, S.3
-
36
-
-
0001471917
-
-
(a) Cokley, T. M.; Harvey, P. J.; Marshall, R. L.; McCluskey, A.; Young, D. J. J. Org. Chem. 1997, 62, 1961.
-
(1997)
J. Org. Chem
, vol.62
, pp. 1961
-
-
Cokley, T.M.1
Harvey, P.J.2
Marshall, R.L.3
McCluskey, A.4
Young, D.J.5
-
37
-
-
0003162888
-
-
(b) Asao, N.; Abe, N.; Tan, Z.; Maruoka, K. Synlett 1998, 377.
-
(1998)
Synlett
, pp. 377
-
-
Asao, N.1
Abe, N.2
Tan, Z.3
Maruoka, K.4
-
39
-
-
37749045926
-
-
Amount of EtOH could be reduced to 0.10 mL without loss of reactivity.
-
Amount of EtOH could be reduced to 0.10 mL without loss of reactivity.
-
-
-
-
40
-
-
0042884007
-
-
Nakajima, M.; Yamamoto, S.; Yamaguchi, Y.; Nakamura, S.; Hashimoto, S. Tetrahedron 2003, 59, 7307.
-
(2003)
Tetrahedron
, vol.59
, pp. 7307
-
-
Nakajima, M.1
Yamamoto, S.2
Yamaguchi, Y.3
Nakamura, S.4
Hashimoto, S.5
|