-
1
-
-
47749122232
-
-
(Eds.: A. Berkessel, H. Gröger), Wiley-VCH, Weinheim
-
Asymmetric Organocatalysis from Biomimetic Concepts to Applications in Asymmetric Synthesis, (Eds.:, A. Berkessel, H. Gröger,), Wiley-VCH, Weinheim, 2004
-
(2004)
Asymmetric Organocatalysis from Biomimetic Concepts to Applications in Asymmetric Synthesis
-
-
-
3
-
-
6044269452
-
-
Angew. Chem. Int. Ed. 2004, 43, 5138-5175
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5138-5175
-
-
-
5
-
-
55049138759
-
-
(Ed.: P. I. Dalko), Wiley-VCH, Weinheim
-
Enantioselective Organocatalysis, (Ed.:, P. I. Dalko,), Wiley-VCH, Weinheim, 2007
-
(2007)
Enantioselective Organocatalysis
-
-
-
6
-
-
38349100690
-
-
S. Mukherjee, J.-W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471-5569
-
(2007)
Chem. Rev.
, vol.107
, pp. 5471-5569
-
-
Mukherjee, S.1
Yang, J.-W.2
Hoffmann, S.3
List, B.4
-
8
-
-
55249111616
-
-
P. Melchiorre, M. Marigo, A. Carlone, G. Bartoli, Angew. Chem. 2008, 120, 6232-6265
-
(2008)
Angew. Chem.
, vol.120
, pp. 6232-6265
-
-
Melchiorre, P.1
Marigo, M.2
Carlone, A.3
Bartoli, G.4
-
9
-
-
53549121402
-
-
Angew. Chem. Int. Ed. 2008, 47, 6138-6171.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 6138-6171
-
-
-
10
-
-
0003980673
-
-
(Eds.: P. T. Anastas, J. C, Warner); Oxford University Press, New York
-
Green Chemistry: Theory and Practice, (Eds.:, P. T. Anastas, J. C, Warner,); Oxford University Press, New York, 1998
-
(1998)
Green Chemistry: Theory and Practice
-
-
-
18
-
-
36749025633
-
-
Angew. Chem. Int. Ed. 2007, 46, 8748-8758
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 8748-8758
-
-
-
20
-
-
33745154819
-
-
K. Ding, J. Med. Chem. 2006, 49, 3432-3436
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3432-3436
-
-
Ding, K.1
-
21
-
-
41649102468
-
-
S. Shangary, D. Qin, D. McEachern, M. Liu, R. S. Miller, S. Qiu, Z. Nikolovska-Coleska, K. Ding, G. Wang, J. Chen, D. Bernard, J. Zhang, Y. Lu, Q. Gu, R. B. Shah, K. J. Pienta, X. Ling, S. Kang, M. Guo, Y. Sun, D. Yang, S. Wang, Proc. Natl. Acad. Sci. USA 2008, 105, 3933-3938
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, pp. 3933-3938
-
-
Shangary, S.1
Qin, D.2
McEachern, D.3
Liu, M.4
Miller, R.S.5
Qiu, S.6
Nikolovska-Coleska, Z.7
Ding, K.8
Wang, G.9
Chen, J.10
Bernard, D.11
Zhang, J.12
Lu, Y.13
Gu, Q.14
Shah, R.B.15
Pienta, K.J.16
Ling, X.17
Kang, S.18
Guo, M.19
Sun, Y.20
Yang, D.21
Wang, S.22
more..
-
22
-
-
77956280420
-
-
M. Rottmann, C. McNamara, B. K. S. Yeung, M. C. S. Lee, B. Zou, B. Russell, P. Seitz, D. M. Plouffe, N. V. Dharia, J. Tan, S. B. Cohen, K. R. Spencer, G. E. González-Páez, S. B. Lakshminarayana, A. Goh, R. Suwanarusk, T. Jegla, E. K. Schmitt, H.-P. Beck, R. Brun, F. Nosten, L. Renia, V. Dartois, T. H. Keller, D. A. Fidock, E. A. Winzeler, T. T. Diagana, Science 2010, 329, 1175-1180
-
(2010)
Science
, vol.329
, pp. 1175-1180
-
-
Rottmann, M.1
McNamara, C.2
Yeung, B.K.S.3
Lee, M.C.S.4
Zou, B.5
Russell, B.6
Seitz, P.7
Plouffe, D.M.8
Dharia, N.V.9
Tan, J.10
Cohen, S.B.11
Spencer, K.R.12
González- Páez, G.E.13
Lakshminarayana, S.B.14
Goh, A.15
Suwanarusk, R.16
Jegla, T.17
Schmitt, E.K.18
Beck, H.-P.19
Brun, R.20
Nosten, F.21
Renia, L.22
Dartois, V.23
Keller, T.H.24
Fidock, D.A.25
Winzeler, E.A.26
Diagana, T.T.27
more..
-
23
-
-
77954271846
-
-
F. Zhou, Y.-L. Liu, J. Zhou, Adv. Synth. Catal. 2010, 352, 1381-1407
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1381-1407
-
-
Zhou, F.1
Liu, Y.-L.2
Zhou, J.3
-
26
-
-
54049101193
-
-
X. Tian, K. Jiang, J. Peng, W. Du, Y.-C. Chen, Org. Lett. 2008, 10, 3583-3586
-
(2008)
Org. Lett.
, vol.10
, pp. 3583-3586
-
-
Tian, X.1
Jiang, K.2
Peng, J.3
Du, W.4
Chen, Y.-C.5
-
27
-
-
67249110016
-
-
For selected examples of amination reactions see
-
L. Cheng, L. Liu, H. Jia, D. Wang, Y.-J. Chen, J. Org. Chem. 2009, 74, 4650-4653. For selected examples of amination reactions see
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4650-4653
-
-
Cheng, L.1
Liu, L.2
Jia, H.3
Wang, D.4
Chen, Y.-J.5
-
28
-
-
70449371812
-
-
Z.-Q. Qian, F. Zhou, T.-P. Du, B.-L. Wang, M. Ding, X.-L. Zhao, J. Zhou, Chem. Commun. 2009, 6753-6755
-
(2009)
Chem. Commun.
, pp. 6753-6755
-
-
Qian, Z.-Q.1
Zhou, F.2
Du, T.-P.3
Wang, B.-L.4
Ding, M.5
Zhao, X.-L.6
Zhou, J.7
-
29
-
-
78650368798
-
-
T. Bui, G. HernÃndez-Torres, C. Milite, C. F. Barbas III, Org. Lett. 2010, 12, 5696-5699
-
(2010)
Org. Lett.
, vol.12
, pp. 5696-5699
-
-
Bui, T.1
Hernãndez-Torres, G.2
Milite, C.3
Iii, C.F.B.4
-
30
-
-
69449091605
-
-
For selected examples of Michael addition reactions see
-
L. Cheng, L. Liu, D. Wang, Y.-J. Chen, Org. Lett. 2009, 11, 3874-3877. For selected examples of Michael addition reactions see
-
(2009)
Org. Lett.
, vol.11
, pp. 3874-3877
-
-
Cheng, L.1
Liu, L.2
Wang, D.3
Chen, Y.-J.4
-
31
-
-
77953878420
-
-
F. Pesciaioli, X. Tian, G. Bencivenni, G. Bartoli, P. Melchiorre, Synlett 2010, 1704-1708
-
(2010)
Synlett
, pp. 1704-1708
-
-
Pesciaioli, F.1
Tian, X.2
Bencivenni, G.3
Bartoli, G.4
Melchiorre, P.5
-
32
-
-
78651258842
-
-
X. Li, S. Luo, J.-P. Cheng, Chem. Eur. J. 2010, 16, 14290-14294
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 14290-14294
-
-
Li, X.1
Luo, S.2
Cheng, J.-P.3
-
33
-
-
68349101812
-
-
P. Galzerano, G. Bencivenni, F. Pesciaioli, A. Mazzanti, B. Giannichi, L. Sambri, G. Bartoli, P. Melchiorre, Chem. Eur. J. 2009, 15, 7846-7849
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 7846-7849
-
-
Galzerano, P.1
Bencivenni, G.2
Pesciaioli, F.3
Mazzanti, A.4
Giannichi, B.5
Sambri, L.6
Bartoli, G.7
Melchiorre, P.8
-
34
-
-
67649600829
-
-
8758- 8759
-
T. Bui, S. Syed, C. F. Barbas III, J. Am. Chem. Soc. 2009, 131, 2009, 8758- 8759
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2009
-
-
Bui, T.1
Syed, S.2
Iii, C.F.B.3
-
35
-
-
70450177483
-
-
R. He, S. Shirakawa, K. Maruoka, J. Am. Chem. Soc. 2009, 131, 166201-166621
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 166201-166621
-
-
He, R.1
Shirakawa, S.2
Maruoka, K.3
-
36
-
-
77149142992
-
-
R. He, C. Ding, K. Maruoka, Angew. Chem. 2009, 121, 4629-4631
-
(2009)
Angew. Chem.
, vol.121
, pp. 4629-4631
-
-
He, R.1
Ding, C.2
Maruoka, K.3
-
37
-
-
70349786240
-
-
For selected examples of hydroxylation reactions see
-
Angew. Chem. Int. Ed. 2009, 48, 4559-4561. For selected examples of hydroxylation reactions see
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 4559-4561
-
-
-
38
-
-
77952578835
-
-
T. Bui, N.-R. Candeias, C. F. Barbas III, J. Am. Chem. Soc. 2010, 132, 5574-5575
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 5574-5575
-
-
Bui, T.1
Candeias, N.-R.2
Iii, C.F.B.3
-
39
-
-
44449174208
-
-
D. Sano, K. Nagata, T. Itoh, Org. Lett. 2008, 10, 1593-1595
-
(2008)
Org. Lett.
, vol.10
, pp. 1593-1595
-
-
Sano, D.1
Nagata, K.2
Itoh, T.3
-
40
-
-
33845919566
-
-
For a selected examples of alkylation reactions see
-
T. Ishimaru, N. Shibata, J. Nagai, S. Nakamura, T. Toru, S. Kanemasa, J. Am. Chem. Soc. 2006, 128, 16488-16489. For a selected examples of alkylation reactions see
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 16488-16489
-
-
Ishimaru, T.1
Shibata, N.2
Nagai, J.3
Nakamura, S.4
Toru, T.5
Kanemasa, S.6
-
41
-
-
67650624055
-
-
For selected examples of cascade reactions see
-
K. Jiang, J. Peng, H.-L. Cuia, Y.-C. Chen, Chem. Commun. 2009, 3955-3957. For selected examples of cascade reactions see
-
(2009)
Chem. Commun.
, pp. 3955-3957
-
-
Jiang, K.1
Peng, J.2
Cuia, H.-L.3
Chen, Y.-C.4
-
43
-
-
79951971249
-
-
F. Pesciaioli, P. Righi, A. Mazzanti, G. Bartoli, G. Bencivenni, Chem. Eur. J. 2011, 17, 2842-2845
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 2842-2845
-
-
Pesciaioli, F.1
Righi, P.2
Mazzanti, A.3
Bartoli, G.4
Bencivenni, G.5
-
44
-
-
77956042533
-
-
A. P. Antonchick, C. Gerding-Reimers, M. Catarinella, M. Schürmann, H. Preut, S. Ziegler, D. Rauh, H. Waldmann, Nature Chem. 2010, 2, 735-740
-
(2010)
Nature Chem.
, vol.2
, pp. 735-740
-
-
Antonchick, A.P.1
Gerding-Reimers, C.2
Catarinella, M.3
Schürmann, M.4
Preut, H.5
Ziegler, S.6
Rauh, D.7
Waldmann, H.8
-
45
-
-
77953572242
-
-
K. Jiang, Z.-J. Jia, Xi. Yin, L. Wu, Y.-C. Chen, Org. Lett. 2010, 12, 2766-2769
-
(2010)
Org. Lett.
, vol.12
, pp. 2766-2769
-
-
Jiang, K.1
Jia, Z.-J.2
Yin, Xi.3
Wu, L.4
Chen, Y.-C.5
-
46
-
-
77149127044
-
-
K. Jiang, Z.-J. Jia, S. Chen, L. Wu, Y.-C. Chen, Chem. Eur. J. 2010, 16, 2852-2856
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 2852-2856
-
-
Jiang, K.1
Jia, Z.-J.2
Chen, S.3
Wu, L.4
Chen, Y.-C.5
-
47
-
-
70349784950
-
-
G. Bencivenni, L.-Y. Wu, A. Mazzanti, B. Giannichi, F. Pesciaioli, M.-P. Song, G. Bartoli, P. Melchiorre, Angew. Chem. 2009, 121, 7336-7339
-
(2009)
Angew. Chem.
, vol.121
, pp. 7336-7339
-
-
Bencivenni, G.1
Wu, L.-Y.2
Mazzanti, A.3
Giannichi, B.4
Pesciaioli, F.5
Song, M.-P.6
Bartoli, G.7
Melchiorre, P.8
-
48
-
-
70349784950
-
-
Angew. Chem. Int. Ed. 2009, 48, 7200-7203.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 7200-7203
-
-
-
49
-
-
77954543828
-
-
To the best of our knowledge only one example describing the organocatalyzed aldol-type reaction of 3-substituted oxindoles with paraformaldehyde has been reported
-
To the best of our knowledge only one example describing the organocatalyzed aldol-type reaction of 3-substituted oxindoles with paraformaldehyde has been reported:, X.-L. Liu, Y.-H. Liao, Z.-J. Wu, L.-F. Cun, X.-M. Zhang, W.-C. Yuan, J. Org. Chem. 2010, 75, 4872-4875
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4872-4875
-
-
Liu, X.-L.1
Liao, Y.-H.2
Wu, Z.-J.3
Cun, L.-F.4
Zhang, X.-M.5
Yuan, W.-C.6
-
50
-
-
53849084173
-
-
for the organocatalyzed direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate see
-
for the organocatalyzed direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate see:, S. Ogawa, N. Shibata, J. Inagaki, S. Nakamura, T. Toru, M. Shiro, Angew. Chem. 2007, 119, 8820-8823
-
(2007)
Angew. Chem.
, vol.119
, pp. 8820-8823
-
-
Ogawa, S.1
Shibata, N.2
Inagaki, J.3
Nakamura, S.4
Toru, T.5
Shiro, M.6
-
51
-
-
36549020091
-
-
Angew. Chem. Int. Ed. 2007, 46, 8666-8669
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 8666-8669
-
-
-
52
-
-
77949727169
-
-
3 complex catalyzed aldol-type reaction of 3-substituted oxindoles with phenylglyoxal derivatives see.
-
3 complex catalyzed aldol-type reaction of 3-substituted oxindoles with phenylglyoxal derivatives see:, K. Shen, X. Liu, K. Zeng, W. Li, X. Hu, L. Lin, X. Feng, Chem. Eur. J. 2010, 16, 3736-3742.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 3736-3742
-
-
Shen, K.1
Liu, X.2
Zeng, K.3
Li, W.4
Hu, X.5
Lin, L.6
Feng, X.7
-
53
-
-
0004049041
-
-
(Eds.: G. M. Coppola, H. F. Schuster), Wiley-VCH, Weinheim.
-
α-Hydroxy acids in Enantioselective Syntheses, (Eds.:, G. M. Coppola, H. F. Schuster,), Wiley-VCH, Weinheim, 1997.
-
(1997)
α-Hydroxy Acids in Enantioselective Syntheses
-
-
-
54
-
-
77950521746
-
-
For a comprehensive review on the Cinchona alkaloids as organocatalysts, see.
-
For a comprehensive review on the Cinchona alkaloids as organocatalysts, see:, T. Marcelli, H. Hiemstra, Synthesis 2010, 1229-1279.
-
(2010)
Synthesis
, pp. 1229-1279
-
-
Marcelli, T.1
Hiemstra, H.2
-
55
-
-
77954117971
-
-
T. Urushima, Y. Yasui, H. Ishikawa, Y. Hayashi, Org. Lett. 2010, 12, 2966-2969
-
(2010)
Org. Lett.
, vol.12
, pp. 2966-2969
-
-
Urushima, T.1
Yasui, Y.2
Ishikawa, H.3
Hayashi, Y.4
-
56
-
-
0034706033
-
-
D. A. Evans, S. W. Tregay, C. S. Burgey, N. A. Paras, T. Vojkovsky, J. Am. Chem. Soc. 2000, 122, 7936-7943
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7936-7943
-
-
Evans, D.A.1
Tregay, S.W.2
Burgey, C.S.3
Paras, N.A.4
Vojkovsky, T.5
-
57
-
-
57149109785
-
-
D. A. Evans, L. Kvarno, T. B. Dunn, A. Beauchemin, B. Raymer, J. A. Mulder, E. J. Olhava, M. Juhl, K. Kagechika, D. A. Favor, J. Am. Chem. Soc. 2008, 130, 16295-16309
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 16295-16309
-
-
Evans, D.A.1
Kvarno, L.2
Dunn, T.B.3
Beauchemin, A.4
Raymer, B.5
Mulder, J.A.6
Olhava, E.J.7
Juhl, M.8
Kagechika, K.9
Favor, D.A.10
-
58
-
-
33746250097
-
-
R. Matsubara, Y. Nakamura, S. Kobayashi, Angew. Chem. 2004, 116, 3320-3322
-
(2004)
Angew. Chem.
, vol.116
, pp. 3320-3322
-
-
Matsubara, R.1
Nakamura, Y.2
Kobayashi, S.3
-
59
-
-
4544373680
-
-
Angew. Chem. Int. Ed. 2004, 43, 3258-3260.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 3258-3260
-
-
-
60
-
-
77953320381
-
-
R. Dalpozzo, G. Bartoli, L. Sambri, P. Melchiorre, Chem. Rev. 2010, 110, 3501-3551
-
(2010)
Chem. Rev.
, vol.110
, pp. 3501-3551
-
-
Dalpozzo, R.1
Bartoli, G.2
Sambri, L.3
Melchiorre, P.4
-
61
-
-
0345168771
-
-
G. Bartoli, M. Bosco, R. Dalpozzo, E. Marcantoni, M. Massaccesi, L. Sambri, Eur. J. Org. Chem. 2003, 4611-4617
-
(2003)
Eur. J. Org. Chem.
, pp. 4611-4617
-
-
Bartoli, G.1
Bosco, M.2
Dalpozzo, R.3
Marcantoni, E.4
Massaccesi, M.5
Sambri, L.6
-
62
-
-
0037240981
-
-
G. Bartoli, M. Bosco, R. Dalpozzo, E. Marcantoni, M. Massaccesi, S. Rinaldi, L. Sambri, Synlett 2003, 39-42.
-
(2003)
Synlett
, pp. 39-42
-
-
Bartoli, G.1
Bosco, M.2
Dalpozzo, R.3
Marcantoni, E.4
Massaccesi, M.5
Rinaldi, S.6
Sambri, L.7
|