-
1
-
-
0037744752
-
-
A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868
-
(2002)
Angew. Chem.
, vol.114
, pp. 1868
-
-
Bøgevig, A.1
Juhl, K.2
Kumaragurubaran, N.3
Zhuang, W.4
Jørgensen, K.A.5
-
6
-
-
73349092127
-
-
P.-M. Liu, C. Chang, R. J. Reddy, Y.-F. Ting, H.-H. Kuan, K. Chen, Eur. J. Org. Chem. 2010, 42.
-
(2010)
Eur. J. Org. Chem.
, pp. 42
-
-
Liu, P.-M.1
Chang, C.2
Reddy, R.J.3
Ting, Y.-F.4
Kuan, H.-H.5
Chen, K.6
-
8
-
-
38349100690
-
-
For a review of enamine catalysis
-
For a review of enamine catalysis, see: S. Mukherjee, J. W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5471
-
-
Mukherjee, S.1
Yang, J.W.2
Hoffmann, S.3
List, B.4
-
10
-
-
38349112828
-
-
For reviews
-
For reviews, see; a) E. A. C. Davie, S. M. Mennen, Y. Xu, S. J. Miller, Chem. Rev. 2007, 107, 5759
-
(2007)
Chem. Rev.
, vol.107
, pp. 5759
-
-
Davie, E.A.C.1
Mennen, S.M.2
Xu, Y.3
Miller, S.J.4
-
12
-
-
4143049101
-
-
a values of proline and N-methylacetoamide in DMSO are ~12 and ~26, respectively
-
a values of proline and N-methylacetoamide in DMSO are ~12 and ~26, respectively, see: a) S. Saito, H. Yamamoto, Acc. Chem. Res. 2004, 37, 570
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 570
-
-
Saito, S.1
Yamamoto, H.2
-
13
-
-
33751553695
-
-
F. G. Bordwell, J. A. Harrelson Jr, T. Y. Lynch, J. Org. Chem. 1990, 55, 3337.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 3337
-
-
Bordwell, F.G.1
Harrelson Jr., J.A.2
Lynch, T.Y.3
-
14
-
-
18244393987
-
-
Wennemers et al. have successfully designed peptide catalysts including a carboxyl group at the side chain of a peptide residue
-
Wennemers et al. have successfully designed peptide catalysts including a carboxyl group at the side chain of a peptide residue; see: a) P. Krattiger, R. Kovasy, J. D. Revell, S. Ivan, H. Wennemers, Org. Lett. 2005, 7, 1101
-
(2005)
Org. Lett.
, vol.7
, pp. 1101
-
-
Krattiger, P.1
Kovasy, R.2
Revell, J.D.3
Ivan, S.4
Wennemers, H.5
-
15
-
-
42649098597
-
-
M. Wiesner, J. D. Revell, S. Tonazzi, H. Wennemers, J. Am. Chem. Soc. 2008, 130, 5610
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 5610
-
-
Wiesner, M.1
Revell, J.D.2
Tonazzi, S.3
Wennemers, H.4
-
16
-
-
54849174500
-
-
M. Wiesner, J. D. Revell, H. Wennemers, Angew. Chem. 2008, 120, 1897
-
(2008)
Angew. Chem.
, vol.120
, pp. 1897
-
-
Wiesner, M.1
Revell, J.D.2
Wennemers, H.3
-
18
-
-
74849117325
-
-
M. Wiesner, G. Upert, G. Angelici, H. Wennemers, J. Am. Chem. Soc. 2010, 132, 6.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 6
-
-
Wiesner, M.1
Upert, G.2
Angelici, G.3
Wennemers, H.4
-
19
-
-
23044482261
-
-
It is reported that the peptide catalyst with a hydroxy group next to an N-terminal prolyl residue is effective for an enantioselective aldol reaction
-
It is reported that the peptide catalyst with a hydroxy group next to an N-terminal prolyl residue is effective for an enantioselective aldol reaction, see: M. R. M. Andreae, A. P. Davis, Tetrahedron: Asymmetry 2005, 16, 2487.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 2487
-
-
Andreae, M.R.M.1
Davis, A.P.2
-
20
-
-
27144559611
-
-
K. Akagawa, S. Sakamoto, K. Kudo, Tetrahedron Lett. 2005, 46, 8185
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8185
-
-
Akagawa, K.1
Sakamoto, S.2
Kudo, K.3
-
21
-
-
47049117184
-
-
K. Akagawa, H. Akabane, S. Sakamoto, K. Kudo, Org. Lett. 2008, 10, 2035
-
(2008)
Org. Lett.
, vol.10
, pp. 2035
-
-
Akagawa, K.1
Akabane, H.2
Sakamoto, S.3
Kudo, K.4
-
22
-
-
68749105801
-
-
K. Akagawa, T. Yamashita, S. Sakamoto, K. Kudo, Tetrahedron Lett. 2009, 50, 5602
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 5602
-
-
Akagawa, K.1
Yamashita, T.2
Sakamoto, S.3
Kudo, K.4
-
23
-
-
77951194201
-
-
K. Akagawa, T. Fujiwara, S. Sakamoto, K. Kudo, Org. Lett. 2010, 12, 1804
-
(2010)
Org. Lett.
, vol.12
, pp. 1804
-
-
Akagawa, K.1
Fujiwara, T.2
Sakamoto, S.3
Kudo, K.4
-
25
-
-
84860726436
-
-
K. Akagawa, R. Suzuki, K. Kudo, Adv. Synth. Catal. 2012, 354, 1280.
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 1280
-
-
Akagawa, K.1
Suzuki, R.2
Kudo, K.3
-
27
-
-
47749137879
-
-
For a review of supported proline and proline derivatives, see
-
For a review of supported proline and proline derivatives, see: M. Gruttadauria, F. Giacalone, R. Noto, Chem. Soc. Rev. 2008, 37, 1666.
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1666
-
-
Gruttadauria, M.1
Giacalone, F.2
Noto, R.3
-
28
-
-
0032564916
-
-
Miller et al. developed the peptide catalysts containing a D-Pro-Aib sequence. For examples
-
Miller et al. developed the peptide catalysts containing a D-Pro-Aib sequence. For examples, see: a) S. J. Miller, G. T. Copeland, N. Papaioannou, T. E. Horstmann, E. M. Ruel, J. Am. Chem. Soc. 1998, 120, 1629
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 1629
-
-
Miller, S.J.1
Copeland, G.T.2
Papaioannou, N.3
Horstmann, T.E.4
Ruel, E.M.5
-
29
-
-
0000089981
-
-
G. T. Copeland, E. R. Jarvo, S. J. Miller, J. Org. Chem. 1998, 63, 6784
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6784
-
-
Copeland, G.T.1
Jarvo, E.R.2
Miller, S.J.3
-
30
-
-
0033596302
-
-
E. R. Jarvo, G. T. Copeland, N. Papaioannou, P. J. Bonitatebus Jr, S. J. Miller, J. Am. Chem. Soc. 1999, 121, 11638
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 11638
-
-
Jarvo, E.R.1
Copeland, G.T.2
Papaioannou, N.3
Bonitatebus Jr., P.J.4
Miller, S.J.5
-
31
-
-
70350461493
-
-
K. W. Fiori, A. L. A. Puchlopek, S. J. Miller, Nature Chem. 2009, 1, 630.
-
(2009)
Nature Chem.
, vol.1
, pp. 630
-
-
Fiori, K.W.1
Puchlopek, A.L.A.2
Miller, S.J.3
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