-
1
-
-
3242702454
-
-
J. M. Lee, Y. Na, H. Han, S. Chang, Chem. Soc. Rev. 2004, 33, 302-312;
-
(2004)
Chem. Soc. Rev.
, vol.33
, pp. 302-312
-
-
Lee, J.M.1
Na, Y.2
Han, H.3
Chang, S.4
-
2
-
-
68949170991
-
-
M. Shibasaki, M. Kanai, S. Matsunaga, N. Kumagai, Acc. Chem. Res. 2009, 42, 1117-1127;
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 1117-1127
-
-
Shibasaki, M.1
Kanai, M.2
Matsunaga, S.3
Kumagai, N.4
-
3
-
-
21544444468
-
-
M. Kanai, N. Kato, E. Ichikawa, M. Shibasaki, Synlett 2005, 1491-1508;
-
(2005)
Synlett
, pp. 1491-1508
-
-
Kanai, M.1
Kato, N.2
Ichikawa, E.3
Shibasaki, M.4
-
5
-
-
5344224096
-
-
J.-A. Ma, D. Cahard, Angew. Chem. 2004, 116, 4666-4683; Angew. Chem. Int. Ed. 2004, 43, 4566-4583.
-
(2004)
Angew. Chem. 2004, 116, 4666-4683; Angew. Chem. Int. Ed.
, vol.43
, pp. 4566-4583
-
-
Ma, J.-A.1
Cahard, D.2
-
6
-
-
79959885758
-
-
For a review, see: S. Piovesana, D. M. ScarpinoSchietroma, M. Bella, Angew. Chem. 2011, 123, 6340-6357; Angew. Chem. Int. Ed. 2011, 50, 6216-6232.
-
(2011)
Angew. Chem. 2011, 123, 6340-6357; Angew. Chem. Int. Ed.
, vol.50
, pp. 6216-6232
-
-
Piovesana, S.1
ScarpinoSchietroma, D.M.2
Bella, M.3
-
9
-
-
83455201108
-
-
N. T. Patil, V. S. Shinde, B. Gajula, Org. Biomol. Chem. 2012, 10, 211-224;
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 211-224
-
-
Patil, N.T.1
Shinde, V.S.2
Gajula, B.3
-
12
-
-
45549094465
-
-
J. T. Binder, B. Crone, T. T. Haug, H. Menz, S. F. Kirsch, Org. Lett. 2008, 10, 1025-1028;
-
(2008)
Org. Lett.
, vol.10
, pp. 1025-1028
-
-
Binder, J.T.1
Crone, B.2
Haug, T.T.3
Menz, H.4
Kirsch, S.F.5
-
13
-
-
45549094298
-
-
T. Yang, A. Ferrali, L. Campbell, D. J. Dixon, Chem. Commun. 2008, 2923-2925.
-
(2008)
Chem. Commun.
, pp. 2923-2925
-
-
Yang, T.1
Ferrali, A.2
Campbell, L.3
Dixon, D.J.4
-
14
-
-
77951228078
-
-
for selected examples involving indium catalysis, see:
-
F. Dénès, A. Pérez-Luna, F. Chemla, Chem. Rev. 2010, 110, 2366-2447; for selected examples involving indium catalysis, see:
-
(2010)
Chem. Rev.
, vol.110
, pp. 2366-2447
-
-
Dénès, F.1
Pérez-Luna, A.2
Chemla, F.3
-
15
-
-
0142183454
-
-
M. Nakamura, K. Endo, E. Nakamura, J. Am. Chem. Soc. 2003, 125, 13002-13003;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 13002-13003
-
-
Nakamura, M.1
Endo, K.2
Nakamura, E.3
-
16
-
-
34547962665
-
-
for selected examples involving copper catalysis, see:
-
P. Angell, P. G. Blazecka, M. Lovdahl, J. Zhang, J. Org. Chem. 2007, 72, 6606-6609; for selected examples involving copper catalysis, see:
-
(2007)
J. Org. Chem.
, vol.72
, pp. 6606-6609
-
-
Angell, P.1
Blazecka, P.G.2
Lovdahl, M.3
Zhang, J.4
-
18
-
-
0033547993
-
-
D. Bouyssi, N. Monteiro, G. Balme, Tetrahedron Lett. 1999, 40, 1297-1300;
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 1297-1300
-
-
Bouyssi, D.1
Monteiro, N.2
Balme, G.3
-
19
-
-
77956917552
-
-
for selected examples involving stoichiometric zinc enolate, see:
-
S. Montel, D. Bouyssi, G. Balme, Adv. Synth. Catal. 2010, 352, 2315-2320; for selected examples involving stoichiometric zinc enolate, see:
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 2315-2320
-
-
Montel, S.1
Bouyssi, D.2
Balme, G.3
-
20
-
-
0031014621
-
-
E. Lorthiois, I. Marek, J.-F. Normant, Tetrahedron Lett. 1997, 38, 89-92;
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 89-92
-
-
Lorthiois, E.1
Marek, I.2
Normant, J.-F.3
-
21
-
-
0001199211
-
-
E. Lorthiois, I. Marek, J.-F. Normant, J. Org. Chem. 1998, 63, 566-574;
-
(1998)
J. Org. Chem.
, vol.63
, pp. 566-574
-
-
Lorthiois, E.1
Marek, I.2
Normant, J.-F.3
-
23
-
-
84867796640
-
-
W. Sun, G. Zhu, C. Wu, L. Hong, R. Wang, Chem. Asian J. 2012, 18, 13959-13963;
-
(2012)
Chem. Asian J.
, vol.18
, pp. 13959-13963
-
-
Sun, W.1
Zhu, G.2
Wu, C.3
Hong, L.4
Wang, R.5
-
24
-
-
82955174771
-
-
W. Sun, G. Zhu, L. Hong, R. Wang, Chem. Eur. J. 2011, 17, 13958-13962;
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 13958-13962
-
-
Sun, W.1
Zhu, G.2
Hong, L.3
Wang, R.4
-
25
-
-
78650292001
-
-
S. Lin, G.-L. Zhao, L. Deiana, J. Sun, Q. Zhang, H. Leijonmarck, A. Córdova, Chem. Eur. J. 2010, 16, 13930-13934;
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 13930-13934
-
-
Lin, S.1
Zhao, G.-L.2
Deiana, L.3
Sun, J.4
Zhang, Q.5
Leijonmarck, H.6
Córdova, A.7
-
26
-
-
75749086819
-
-
G.-L. Zhao, F. Ullah, L. Deiana, S. Lin, Q. Zhang, J. Sun, I. Ibrahem, P. Dziedzic, A. Córdova, Chem. Eur. J. 2010, 16, 1585-1591;
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 1585-1591
-
-
Zhao, G.-L.1
Ullah, F.2
Deiana, L.3
Lin, S.4
Zhang, Q.5
Sun, J.6
Ibrahem, I.7
Dziedzic, P.8
Córdova, A.9
-
27
-
-
75749120984
-
-
K. L. Jensen, P. T. Franke, C. Arróniz, S. Kobbelgaard, K. A. Jørgensen, Chem. Eur. J. 2010, 16, 1750-1753.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 1750-1753
-
-
Jensen, K.L.1
Franke, P.T.2
Arróniz, C.3
Kobbelgaard, S.4
Jørgensen, K.A.5
-
28
-
-
84880959220
-
-
[4a].
-
[4a].
-
-
-
-
29
-
-
77952960882
-
-
B. Montaignac, M. R. Vitale, V. Michelet, V. Ratovelomanana-Vidal, Org. Lett. 2010, 12, 2582-2585;
-
(2010)
Org. Lett.
, vol.12
, pp. 2582-2585
-
-
Montaignac, B.1
Vitale, M.R.2
Michelet, V.3
Ratovelomanana-Vidal, V.4
-
30
-
-
78650298803
-
-
B. Montaignac, M. R. Vitale, V. Ratovelomanana-Vidal, V. Michelet, J. Org. Chem. 2010, 75, 8322-8325;
-
(2010)
J. Org. Chem.
, vol.75
, pp. 8322-8325
-
-
Montaignac, B.1
Vitale, M.R.2
Ratovelomanana-Vidal, V.3
Michelet, V.4
-
31
-
-
79960314487
-
-
B. Montaignac, M. R. Vitale, V. Ratovelomanana-Vidal, V. Michelet, Eur. J. Org. Chem. 2011, 3723-3727;
-
(2011)
Eur. J. Org. Chem.
, pp. 3723-3727
-
-
Montaignac, B.1
Vitale, M.R.2
Ratovelomanana-Vidal, V.3
Michelet, V.4
-
32
-
-
84857608277
-
-
B. Montaignac, V. Ostlund, M. R. Vitale, V. Ratovelomanana-Vidal, V. Michelet, Org. Biomol. Chem. 2012, 10, 2300-2306.
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 2300-2306
-
-
Montaignac, B.1
Ostlund, V.2
Vitale, M.R.3
Ratovelomanana-Vidal, V.4
Michelet, V.5
-
33
-
-
84880958095
-
-
For reviews, see:
-
For reviews, see:
-
-
-
-
40
-
-
84862214933
-
-
B. Montaignac, C. Praveen, M. R. Vitale, V. Michelet, V. Ratovelomanana-Vidal, Chem. Commun. 2012, 48, 6559-6561.
-
(2012)
Chem. Commun.
, vol.48
, pp. 6559-6561
-
-
Montaignac, B.1
Praveen, C.2
Vitale, M.R.3
Michelet, V.4
Ratovelomanana-Vidal, V.5
-
41
-
-
84880930307
-
-
For reviews dealing with indium(III)-catalyzed processes, see:
-
For reviews dealing with indium(III)-catalyzed processes, see:
-
-
-
-
44
-
-
74949122785
-
-
J. S. Yadav, A. Antony, J. George, B. V. SubbaReddy, Eur. J. Org. Chem. 2010, 591-605.
-
(2010)
Eur. J. Org. Chem.
, pp. 591-605
-
-
Yadav, J.S.1
Antony, A.2
George, J.3
SubbaReddy, B.V.4
-
45
-
-
84880952860
-
-
For examples of indium-catalyzed asymmetric carbonyl-ene reactions, see:
-
For examples of indium-catalyzed asymmetric carbonyl-ene reactions, see:
-
-
-
-
46
-
-
77956354236
-
-
J. F. Zhao, B. H. Tan, M. K. Zhu, T. B. W. Tjan, T. P. Loh, Adv. Synth. Catal. 2010, 352, 2085-2088;
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 2085-2088
-
-
Zhao, J.F.1
Tan, B.H.2
Zhu, M.K.3
Tjan, T.B.W.4
Loh, T.P.5
-
47
-
-
57549090773
-
-
For examples of indium catalyzed asymmetric Mukayama-aldol reactions, see:
-
J.-F. Zhao, H.-Y. Tsui, P.-J. Wu, J. Lu, T.-P. Loh, J. Am. Chem. Soc. 2008, 130, 16492-16493; For examples of indium catalyzed asymmetric Mukayama-aldol reactions, see:
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 16492-16493
-
-
Zhao, J.-F.1
Tsui, H.-Y.2
Wu, P.-J.3
Lu, J.4
Loh, T.-P.5
-
48
-
-
79955583920
-
-
J.-F. Zhao, B.-H. Tan, T.-P. Loh, Chem. Sci. 2011, 2, 349-352;
-
(2011)
Chem. Sci.
, vol.2
, pp. 349-352
-
-
Zhao, J.-F.1
Tan, B.-H.2
Loh, T.-P.3
-
49
-
-
33646691032
-
-
for examples of indium catalysed asymmetric allylation reactions, see:
-
F. Fu, Y.-C. Teo, T.-P. Loh, Tetrahedron Lett. 2006, 47, 4267-4269; for examples of indium catalysed asymmetric allylation reactions, see:
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 4267-4269
-
-
Fu, F.1
Teo, Y.-C.2
Loh, T.-P.3
-
50
-
-
25144446723
-
-
J. Lu, M.-L. Hong, S.-J. Ji, Y.-C. Teo, T.-P. Loh, Chem. Commun. 2005, 4217-4218;
-
(2005)
Chem. Commun.
, pp. 4217-4218
-
-
Lu, J.1
Hong, M.-L.2
Ji, S.-J.3
Teo, Y.-C.4
Loh, T.-P.5
-
53
-
-
0032506564
-
-
Š. Vyskočil, M. Smrčina, P. Kočovský, Tetrahedron Lett. 1998, 39, 9289-9292.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9289-9292
-
-
Vyskočil, S.1
Smrčina, M.2
Kočovský, P.3
-
54
-
-
0000171979
-
-
R. Schmid, E. A. Broger, M. Cereghetti, Y. Crameri, J. Foricher, M. Lalonde, R. K. Müller, M. Scalone, G. Schoettel, U. Zutter, Pure Appl. Chem. 1996, 68, 131-138.
-
(1996)
Pure Appl. Chem.
, vol.68
, pp. 131-138
-
-
Schmid, R.1
Broger, E.A.2
Cereghetti, M.3
Crameri, Y.4
Foricher, J.5
Lalonde, M.6
Müller, R.K.7
Scalone, M.8
Schoettel, G.9
Zutter, U.10
-
55
-
-
70349847238
-
-
2 to L ratio was used by Nishibayashi etal. for the copper-catalyzed enantioselective ring-opening reaction of ethynyl epoxides
-
2 to L ratio was used by Nishibayashi etal. for the copper-catalyzed enantioselective ring-opening reaction of ethynyl epoxides: G. Hattori, A. Yoshida, Y. Miyake, Y. Nishibayashi, J. Org. Chem. 2009, 74, 7603-7607.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 7603-7607
-
-
Hattori, G.1
Yoshida, A.2
Miyake, Y.3
Nishibayashi, Y.4
-
56
-
-
84880955568
-
-
The absolute stereochemistry of the major enantiomer of pyrrolidines 6a-6j was attributed by analogy to cyclopentanes.
-
The absolute stereochemistry of the major enantiomer of pyrrolidines 6a-6j was attributed by analogy to cyclopentanes.
-
-
-
-
57
-
-
0029119899
-
-
T. Fukuyama, C.-K. Jow, M. Cheung, Tetrahedron Lett. 1995, 36, 6373-6374.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 6373-6374
-
-
Fukuyama, T.1
Jow, C.-K.2
Cheung, M.3
-
58
-
-
84880931552
-
-
[8]
-
[8]
-
-
-
-
59
-
-
84880946096
-
-
The intervention of an enol-type mechanism has been ruled out because the use of a chiral primary amine instead of cyclohexylamine significantly affected the enantioselectivity outcome of the reaction (see the Supporting Information).
-
The intervention of an enol-type mechanism has been ruled out because the use of a chiral primary amine instead of cyclohexylamine significantly affected the enantioselectivity outcome of the reaction (see the Supporting Information).
-
-
-
-
60
-
-
84880936666
-
-
2 coordination of the terminal alkyne to copper(I) complexes, see:
-
2 coordination of the terminal alkyne to copper(I) complexes, see:
-
-
-
-
63
-
-
0036882872
-
-
C. W. Baxter, T. C. Higgs, A. C. Jones, S. Parsons, P. J. Bailey, P. A. Tasker, J. Chem. Soc. Dalton Trans. 2002, 4395-4401;
-
(2002)
J. Chem. Soc. Dalton Trans.
, pp. 4395-4401
-
-
Baxter, C.W.1
Higgs, T.C.2
Jones, A.C.3
Parsons, S.4
Bailey, P.J.5
Tasker, P.A.6
-
64
-
-
37049075291
-
-
M. Munakata, S. Kitagawa, I. Kawada, M. Maekawa, H. Shimono, J. Chem. Soc. Dalton Trans. 1992, 2225-2230.
-
(1992)
J. Chem. Soc. Dalton Trans.
, pp. 2225-2230
-
-
Munakata, M.1
Kitagawa, S.2
Kawada, I.3
Maekawa, M.4
Shimono, H.5
-
65
-
-
84880963987
-
-
2 coordination of the terminal alkyne to copper(I) complexes, see:
-
2 coordination of the terminal alkyne to copper(I) complexes, see:
-
-
-
-
66
-
-
84870032433
-
-
H. Lang, A. Jakob, B. Milde, Organometallics 2012, 31, 7661-7693;
-
(2012)
Organometallics
, vol.31
, pp. 7661-7693
-
-
Lang, H.1
Jakob, A.2
Milde, B.3
-
67
-
-
5344280743
-
-
H. Lang, K. Köhler, S. Blau, Coord. Chem. Rev. 1995, 143, 113-168.
-
(1995)
Coord. Chem. Rev.
, vol.143
, pp. 113-168
-
-
Lang, H.1
Köhler, K.2
Blau, S.3
-
68
-
-
84880943585
-
-
The cis stereochemistry of 8a was determined on the basis of NOESY experiments (see the Supporting Information for more details).
-
The cis stereochemistry of 8a was determined on the basis of NOESY experiments (see the Supporting Information for more details).
-
-
-
|