-
1
-
-
80051735595
-
-
For examples of such pharmacophores, see
-
For examples of such pharmacophores, see
-
-
-
-
2
-
-
0034687224
-
-
N. Plobeck, D. Delorme, Z.-Y. Wei, H. Yang, F. Zhou, P. Schwarz, L. Gawell, H. Gagnon, B. Pelcman, R. Schmidt, S.-Y. Yue, C. Walpole, W. Brown, E. Zhou, M. Labarre, K. Payza, S. St-Onge, A. Kamassah, P.-E. Morin, D. Projean, J. Ducharme, E. Roberts, J. Med. Chem. 2000, 43, 3878
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3878
-
-
Plobeck, N.1
Delorme, D.2
Wei, Z.-Y.3
Yang, H.4
Zhou, F.5
Schwarz, P.6
Gawell, L.7
Gagnon, H.8
Pelcman, B.9
Schmidt, R.10
Yue, S.-Y.11
Walpole, C.12
Brown, W.13
Zhou, E.14
Labarre, M.15
Payza, K.16
St-Onge, S.17
Kamassah, A.18
Morin, P.-E.19
Projean, D.20
Ducharme, J.21
Roberts, E.22
more..
-
3
-
-
53349162216
-
-
S. Jolidon, D. Alberati, A. Dowle, H. Fischezr, D. Hainzl, R. Narquizian, R. Norcross, E. Pinard, Bioorg. Med. Chem. Lett. 2008, 18, 5533.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5533
-
-
Jolidon, S.1
Alberati, D.2
Dowle, A.3
Fischezr, H.4
Hainzl, D.5
Narquizian, R.6
Norcross, R.7
Pinard, E.8
-
4
-
-
80051744067
-
-
For chiral auxiliary based addition of organometallic reagents to imines, see
-
For chiral auxiliary based addition of organometallic reagents to imines, see
-
-
-
-
6
-
-
0037016979
-
-
D. A. Pflum, D. Krishnamurthy, Z. Han, S. A. Wald, C. H. Senanayake, Tetrahedron Lett. 2002, 43, 923
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 923
-
-
Pflum, D.A.1
Krishnamurthy, D.2
Han, Z.3
Wald, S.A.4
Senanayake, C.H.5
-
8
-
-
13644262210
-
-
By substrate-controlled stereospecific intramolecular aryl transfer
-
D. J. Weix, Y. Shi, J. A. Ellman, J. Am. Chem. Soc. 2005, 127, 1092; By substrate-controlled stereospecific intramolecular aryl transfer
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 1092
-
-
Weix, D.J.1
Shi, Y.2
Ellman, J.A.3
-
11
-
-
80051734473
-
-
For Rh-catalyzed chiral-ligand-based enantioselective arylations of arylimines with aryl borons reagents, see
-
For Rh-catalyzed chiral-ligand-based enantioselective arylations of arylimines with aryl borons reagents, see
-
-
-
-
12
-
-
3042817456
-
-
M. Kuriyama, T. Soeta, X. Hao, Q. Chen, K. Tomioka, J. Am. Chem. Soc. 2004, 126, 8128
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8128
-
-
Kuriyama, M.1
Soeta, T.2
Hao, X.3
Chen, Q.4
Tomioka, K.5
-
13
-
-
6444231736
-
-
N. Tokunaga, Y. Otomaru, K. Okamoto, K. Ueyama, R. Shantani, T. Hayashi, J. Am. Chem. Soc. 2004, 126, 13584
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13584
-
-
Tokunaga, N.1
Otomaru, Y.2
Okamoto, K.3
Ueyama, K.4
Shantani, R.5
Hayashi, T.6
-
14
-
-
13444262183
-
-
Y. Otomaru, N. Tokunaga, R. Shantani, T. Hayashi, Org. Lett. 2005, 7, 307
-
(2005)
Org. Lett.
, vol.7
, pp. 307
-
-
Otomaru, Y.1
Tokunaga, N.2
Shantani, R.3
Hayashi, T.4
-
15
-
-
33845950335
-
-
R. B. C. Jagt, P. Y. Toullec, D. Geerdink, J. G. de Vries, B. L. Feringa, A. J. Minnaard, Angew. Chem. 2006, 118, 2855
-
(2006)
Angew. Chem.
, vol.118
, pp. 2855
-
-
Jagt, R.B.C.1
Toullec, P.Y.2
Geerdink, D.3
De Vries, J.G.4
Feringa, B.L.5
Minnaard, A.J.6
-
17
-
-
33745541260
-
-
H.-F. Duan, Y.-X. Jia, L.-X. Wang, Q.-L. Zhou, Org. Lett. 2006, 8, 2567
-
(2006)
Org. Lett.
, vol.8
, pp. 2567
-
-
Duan, H.-F.1
Jia, Y.-X.2
Wang, L.-X.3
Zhou, Q.-L.4
-
18
-
-
37249065123
-
-
H. Nakagawa, J. C. Rech, R. W. Sindelar, J. A. Ellman, Org. Lett. 2007, 9, 5155
-
(2007)
Org. Lett.
, vol.9
, pp. 5155
-
-
Nakagawa, H.1
Rech, J.C.2
Sindelar, R.W.3
Ellman, J.A.4
-
19
-
-
34247897083
-
-
Z.-Q. Wang, C.-G. Feng, M.-H. Xu, G.-Q. Lin, J. Am. Chem. Soc. 2007, 129, 5336
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 5336
-
-
Wang, Z.-Q.1
Feng, C.-G.2
Xu, M.-H.3
Lin, G.-Q.4
-
20
-
-
58549106779
-
-
K. Kurihara, Y. Yamamoto, N. Miyaura, Adv. Synth. Catal. 2009, 351, 260
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 260
-
-
Kurihara, K.1
Yamamoto, Y.2
Miyaura, N.3
-
21
-
-
70350192265
-
-
X. Hao, M. Kuriyama, Q. Chen, Y. Yamamoto, K. Yamada, K. Tomioka, Org. Lett. 2009, 11, 4470
-
(2009)
Org. Lett.
, vol.11
, pp. 4470
-
-
Hao, X.1
Kuriyama, M.2
Chen, Q.3
Yamamoto, Y.4
Yamada, K.5
Tomioka, K.6
-
22
-
-
70349283054
-
-
for Rh-catalyzed arylation of N-tosylarylimines with arylstannanes, see
-
K. Okamoto, T. Hayashi, V. H. Rawal, Chem. Commun. 2009, 4815; for Rh-catalyzed arylation of N-tosylarylimines with arylstannanes, see
-
(2009)
Chem. Commun.
, pp. 4815
-
-
Okamoto, K.1
Hayashi, T.2
Rawal, V.H.3
-
24
-
-
0035953001
-
-
for Rh-catalyzed arylation of N-tosylarylimines with arylzinc reagents, see
-
T. Hayashi, M. Ishigedani, Tetrahedron 2001, 57, 2589; for Rh-catalyzed arylation of N-tosylarylimines with arylzinc reagents, see
-
(2001)
Tetrahedron
, vol.57
, pp. 2589
-
-
Hayashi, T.1
Ishigedani, M.2
-
25
-
-
0037664948
-
-
N. Hermanns, S. Dahmen, C. Bolm, S. Bräse, Angew. Chem. 2002, 114, 3844
-
(2002)
Angew. Chem.
, vol.114
, pp. 3844
-
-
Hermanns, N.1
Dahmen, S.2
Bolm, C.3
Bräse, S.4
-
26
-
-
0037020423
-
-
for Rh-catalyzed arylation of arylimines with aryl titanium reagents, see
-
Angew. Chem. Int. Ed. 2002, 41, 3692; for Rh-catalyzed arylation of arylimines with aryl titanium reagents, see
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 3692
-
-
-
28
-
-
10044235122
-
-
3 complex followed by displacement of a hydroxy group by an amino group, see
-
3 complex followed by displacement of a hydroxy group by an amino group, see
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6125
-
-
-
30
-
-
80051767048
-
-
For reviews about asymmetric additions of organometallic reagents to Ci N bonds, see
-
For reviews about asymmetric additions of organometallic reagents to Ci N bonds, see
-
-
-
-
35
-
-
0000696874
-
-
(Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, Germany, Chapter
-
H.-U. Blaser, F. Spindler, in Comprehensive Asymmetric Catalysis, Vol. 1 (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Berlin, Germany, 1999, Chapter 6.2
-
(1999)
Comprehensive Asymmetric Catalysis, Vol. 1
-
-
Blaser, H.-U.1
Spindler, F.2
-
36
-
-
80051757352
-
-
(Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, Germany, Chapter
-
H. Nishiyama, in Comprehensive Asymmetric Catalysis, Vol. 1 (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Berlin, Germany, 1999, Chapter 6.3
-
(1999)
Comprehensive Asymmetric Catalysis, Vol. 1
-
-
Nishiyama, H.1
-
37
-
-
38349146288
-
-
(Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, Germany, Chapter
-
T. Ohkuma, R. Noyori, in Comprehensive Asymmetric Catalysis, Vol. 1 (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Berlin, Germany, 2003, Chapter 6.2
-
(2003)
Comprehensive Asymmetric Catalysis, Vol. 1
-
-
Ohkuma, T.1
Noyori, R.2
-
38
-
-
38349146288
-
-
(Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, Germany, Chapter
-
T. Ohkuma, R. Noyori, in Comprehensive Asymmetric Catalysis, Vol. 1 (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Berlin, Germany, 2003, Chapter 6.3
-
(2003)
Comprehensive Asymmetric Catalysis, Vol. 1
-
-
Ohkuma, T.1
Noyori, R.2
-
41
-
-
80051773435
-
-
For transition-metal-catalyzed hydrogen-transfer reductive amination to primary amines, see
-
For transition-metal-catalyzed hydrogen-transfer reductive amination to primary amines, see
-
-
-
-
43
-
-
0345276532
-
-
for the enantioselective reduction of trifluoromethylated ketimines with borane-chiral oxazaborolidine (OAB), see
-
Angew. Chem. Int. Ed. 2003, 42, 5472; for the enantioselective reduction of trifluoromethylated ketimines with borane-chiral oxazaborolidine (OAB), see
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 5472
-
-
-
44
-
-
13444302540
-
-
for a chiral Ir-complex-catalyzed hydrogenation
-
F. Gosselin, P. D. O'Shea, S. Roy, R. A. Reamer, C. Chen, R. P. Volante, Org. Lett. 2005, 7, 355; for a chiral Ir-complex-catalyzed hydrogenation
-
(2005)
Org. Lett.
, vol.7
, pp. 355
-
-
Gosselin, F.1
O'Shea, P.D.2
Roy, S.3
Reamer, R.A.4
Chen, C.5
Volante, R.P.6
-
45
-
-
67651211401
-
-
G. Hou, F. Gosselin, W. Li, J. C. McWilliams, Y. Sun, M. Weisel, P. D. O'Shea, C. Chen, I. W. Davies, X. Zhang, J. Am. Chem. Soc. 2009, 131, 9882
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 9882
-
-
Hou, G.1
Gosselin, F.2
Li, W.3
McWilliams, J.C.4
Sun, Y.5
Weisel, M.6
O'Shea, P.D.7
Chen, C.8
Davies, I.W.9
Zhang, X.10
-
46
-
-
77950788901
-
-
for a chiral Rh-complex-catalyzed hydrogenation of unprotected enamines, see
-
G. Hou, R. Tao, Y. Sun, X. Zhang, F. Gosselin, J. Am. Chem. Soc. 2010, 132, 2124; for a chiral Rh-complex-catalyzed hydrogenation of unprotected enamines, see
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 2124
-
-
Hou, G.1
Tao, R.2
Sun, Y.3
Zhang, X.4
Gosselin, F.5
-
47
-
-
4043110495
-
-
Y. Hsiao, N. R. Rivera, T. Rosner, S. W. Krska, E. Njolito, F. Wang, Y. Sun, J. D. Armstrong III, E. J. J. Grabowski, R. D. Tillyer, F. Spindler, Malan, J. Am. Chem. Soc. 2004, 126, 9918.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9918
-
-
Hsiao, Y.1
Rivera, N.R.2
Rosner, T.3
Krska, S.W.4
Njolito, E.5
Wang, F.6
Sun, Y.7
Armstrong III, J.D.8
Grabowski, E.J.J.9
Tillyer, R.D.10
Spindler, F.11
Malan12
-
48
-
-
77957832563
-
-
T. B. Nguyen, H. Bousserouel, Q. Wang, F. Guéritte, Org. Lett. 2010, 12, 4705
-
(2010)
Org. Lett.
, vol.12
, pp. 4705
-
-
Nguyen, T.B.1
Bousserouel, H.2
Wang, Q.3
Guéritte, F.4
-
49
-
-
79951834837
-
-
T. B. Nguyen, H. Bousserouel, Q. Wang, F. Guéritte, Adv. Synth. Catal. 2011, 353, 257.
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 257
-
-
Nguyen, T.B.1
Bousserouel, H.2
Wang, Q.3
Guéritte, F.4
-
50
-
-
80051741496
-
-
For chiral phosphoric-acid-catalyzed enantioselective reduction of N-protected aryl alkyl ketimines using a Hantzsch ester as the reducing agent, see
-
For chiral phosphoric-acid-catalyzed enantioselective reduction of N-protected aryl alkyl ketimines using a Hantzsch ester as the reducing agent, see
-
-
-
-
51
-
-
24044465512
-
-
M. Rueping, E. Sugiono, C. Azap, T. Theissmann, M. Bolte, Org. Lett. 2005, 7, 3781
-
(2005)
Org. Lett.
, vol.7
, pp. 3781
-
-
Rueping, M.1
Sugiono, E.2
Azap, C.3
Theissmann, T.4
Bolte, M.5
-
52
-
-
33746182597
-
-
S. Hoffmann, A. M. Seayad, B. List, Angew. Chem. 2005, 117, 7590
-
(2005)
Angew. Chem.
, vol.117
, pp. 7590
-
-
Hoffmann, S.1
Seayad, A.M.2
List, B.3
-
54
-
-
30744477746
-
-
R. I. Storer, D. E. Carrera, Y. Ni, D. W. C. MacMillan, J. Am. Chem. Soc. 2006, 128, 84
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 84
-
-
Storer, R.I.1
Carrera, D.E.2
Ni, Y.3
MacMillan, D.W.C.4
-
55
-
-
33749534513
-
-
S. Hoffmann, M. Nicoletti, B. List, J. Am. Chem. Soc. 2006, 128, 13074.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13074
-
-
Hoffmann, S.1
Nicoletti, M.2
List, B.3
-
56
-
-
80051766656
-
-
For the first asymmetric (63% ee) organocatalytic Hantzsch ester reduction of imines, see
-
For the first asymmetric (63% ee) organocatalytic Hantzsch ester reduction of imines, see
-
-
-
-
57
-
-
30744457769
-
-
for reviews of enantioselective organocatalytic transfer hydrogenation using Hantzsch dihydropyridines, see
-
S. Singh, U. K. Batra, Indian J. Chem. Sect. B 1989, 28, 1; for reviews of enantioselective organocatalytic transfer hydrogenation using Hantzsch dihydropyridines, see
-
(1989)
Indian J. Chem. Sect. B
, vol.28
, pp. 1
-
-
Singh, S.1
Batra, U.K.2
-
59
-
-
38049089797
-
-
S. G. Ouellet, A. M. Walji, D. W. C. Macmillan, Acc. Chem. Res. 2007, 40, 1327
-
(2007)
Acc. Chem. Res.
, vol.40
, pp. 1327
-
-
Ouellet, S.G.1
Walji, A.M.2
MacMillan, D.W.C.3
-
61
-
-
54549105366
-
-
for a study of the hydride-donor abilities of 1,4-dihydropyridines, see
-
C. Wang, X. Wu, J. Xiao, Chem. Asian J. 2008, 3, 1750; for a study of the hydride-donor abilities of 1,4-dihydropyridines, see
-
(2008)
Chem. Asian J.
, vol.3
, pp. 1750
-
-
Wang, C.1
Wu, X.2
Xiao, J.3
-
64
-
-
33750175116
-
-
M. Rueping, A. P. Antonchick, T. Theissmann, Angew. Chem. 2006, 118, 3765
-
(2006)
Angew. Chem.
, vol.118
, pp. 3765
-
-
Rueping, M.1
Antonchick, A.P.2
Theissmann, T.3
-
66
-
-
33845329144
-
-
M. Rueping, A. P. Antonchick, T. Theissmann, Angew. Chem. 2006, 118, 6903
-
(2006)
Angew. Chem.
, vol.118
, pp. 6903
-
-
Rueping, M.1
Antonchick, A.P.2
Theissmann, T.3
-
70
-
-
34248524344
-
-
G. Li, Y. Liang, J. C. Antilla, J. Am. Chem. Soc. 2007, 129, 5830
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 5830
-
-
Li, G.1
Liang, Y.2
Antilla, J.C.3
-
72
-
-
34547207611
-
-
Q. Kang, Z.-A. Zhao, S.-L. You, Adv. Synth. Catal. 2007, 349, 1657
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1657
-
-
Kang, Q.1
Zhao, Z.-A.2
You, S.-L.3
-
73
-
-
53549126171
-
-
Q.-S. Guo, D.-M. Du, J. Xu, Angew. Chem. 2008, 120, 771
-
(2008)
Angew. Chem.
, vol.120
, pp. 771
-
-
Guo, Q.-S.1
Du, D.-M.2
Xu, J.3
-
75
-
-
53249093355
-
-
M. Rueping, T. Theissmann, S. Raja, J. W. Bats, Adv. Synth. Catal. 2008, 350, 1001
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1001
-
-
Rueping, M.1
Theissmann, T.2
Raja, S.3
Bats, J.W.4
-
76
-
-
47049087920
-
-
Q. Kang, Z.-A. Zhao, S.-L. You, Org. Lett. 2008, 10, 2031
-
(2008)
Org. Lett.
, vol.10
, pp. 2031
-
-
Kang, Q.1
Zhao, Z.-A.2
You, S.-L.3
-
80
-
-
67649637554
-
-
Z.-Y. Han, H. Xiao, L.-Z. Gong, Bioorg. Med. Chem. Lett. 2009, 19, 3729
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3729
-
-
Han, Z.-Y.1
Xiao, H.2
Gong, L.-Z.3
-
81
-
-
77149179738
-
-
M. Rueping, E. Sugiono, A. Steck, T. Theissmann, Adv. Synth. Catal. 2010, 352, 281
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 281
-
-
Rueping, M.1
Sugiono, E.2
Steck, A.3
Theissmann, T.4
-
82
-
-
77955656206
-
-
M. Rueping, M. Stoeckel, E. Sugiono, T. Theissmann, Tetrahedron 2010, 66, 6565
-
(2010)
Tetrahedron
, vol.66
, pp. 6565
-
-
Rueping, M.1
Stoeckel, M.2
Sugiono, E.3
Theissmann, T.4
-
83
-
-
77149176225
-
-
M. Rueping, F. Tato, F. R. Schoepke, Chem. Eur. J. 2010, 16, 2688
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 2688
-
-
Rueping, M.1
Tato, F.2
Schoepke, F.R.3
-
84
-
-
77957856021
-
-
For chiral phosphoric-acid-catalyzed transfer hydrogenation with benzothiozoline, see
-
M. Rueping, C. Brinkmann, A. P. Antonchick, I. Atodiresei, Org. Lett. 2010, 12, 4604. For chiral phosphoric-acid-catalyzed transfer hydrogenation with benzothiozoline, see
-
(2010)
Org. Lett.
, vol.12
, pp. 4604
-
-
Rueping, M.1
Brinkmann, C.2
Antonchick, A.P.3
Atodiresei, I.4
-
86
-
-
80051746421
-
-
For reviews on chiral phosphoric acid catalysis, see
-
For reviews on chiral phosphoric acid catalysis, see
-
-
-
-
92
-
-
77955795989
-
-
for a reliable synthesis of free phosphoric acid and its catalytic activity, see
-
for a reliable synthesis of free phosphoric acid and its catalytic activity, see:, M. Hatano, K. Moriyama, T. Maki, K. Ishihara, Angew. Chem. 2010, 122, 3911
-
(2010)
Angew. Chem.
, vol.122
, pp. 3911
-
-
Hatano, M.1
Moriyama, K.2
Maki, T.3
Ishihara, K.4
-
94
-
-
80051734855
-
-
For selected recent examples on chiral phosphoric acids, see
-
For selected recent examples on chiral phosphoric acids, see
-
-
-
-
95
-
-
6044226554
-
-
T. Akiyama, J. Itoh, K. Yokota, K. Fuchibe, Angew. Chem. 2004, 116, 1592
-
(2004)
Angew. Chem.
, vol.116
, pp. 1592
-
-
Akiyama, T.1
Itoh, J.2
Yokota, K.3
Fuchibe, K.4
-
98
-
-
27844464898
-
-
G. B. Rowland, H. Zhang, E. B. Rowland, S. Chennamadhavuni, Y. Wang, J. C. Antilla, J. Am. Chem. Soc. 2005, 127, 15696
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15696
-
-
Rowland, G.B.1
Zhang, H.2
Rowland, E.B.3
Chennamadhavuni, S.4
Wang, Y.5
Antilla, J.C.6
-
99
-
-
33746323600
-
-
M. Rueping, E. Sugiono, C. Azap, Angew. Chem. 2006, 118, 2679
-
(2006)
Angew. Chem.
, vol.118
, pp. 2679
-
-
Rueping, M.1
Sugiono, E.2
Azap, C.3
-
101
-
-
33845205051
-
-
X.-H. Chen, X.-Y. Xu, H. Liu, L.-F. Cun, L.-Z. Gong, J. Am. Chem. Soc. 2006, 128, 14802
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 14802
-
-
Chen, X.-H.1
Xu, X.-Y.2
Liu, H.3
Cun, L.-F.4
Gong, L.-Z.5
-
102
-
-
33846972343
-
-
Q. Kang, Z.-A. Zhao, S.-L. You, J. Am. Chem. Soc. 2007, 129, 1484
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 1484
-
-
Kang, Q.1
Zhao, Z.-A.2
You, S.-L.3
-
103
-
-
38849129202
-
-
Y.-X. Jia, J. Zhong, S.-F. Zhu, C.-M. Zhang, Q. L. Zhou, Angew. Chem. 2007, 119, 5661
-
(2007)
Angew. Chem.
, vol.119
, pp. 5661
-
-
Jia, Y.-X.1
Zhong, J.2
Zhu, S.-F.3
Zhang, C.-M.4
Zhou, Q.L.5
-
105
-
-
53249096987
-
-
M. J. Wanner, R. N. S. van der Haas, K. R. de Cuba, J. H. van Maarseveen, H. Hiemstra, Angew. Chem. 2007, 119, 7629
-
(2007)
Angew. Chem.
, vol.119
, pp. 7629
-
-
Wanner, M.J.1
Van Der Haas, R.N.S.2
De Cuba, K.R.3
Van Maarseveen, J.H.4
Hiemstra, H.5
-
110
-
-
55049118534
-
-
D. Enders, A. A. Narine, F. Toulgoat, T. Bisschops, Angew. Chem. 2008, 120, 5744
-
(2008)
Angew. Chem.
, vol.120
, pp. 5744
-
-
Enders, D.1
Narine, A.A.2
Toulgoat, F.3
Bisschops, T.4
-
113
-
-
67749110116
-
-
H. Liu, G. Dagousset, G. Masson, J. Zhu, J. Am. Chem. Soc. 2009, 131, 4598
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 4598
-
-
Liu, H.1
Dagousset, G.2
Masson, G.3
Zhu, J.4
-
114
-
-
67749118135
-
-
M. Terada, H. Tanaka, K. Sorimachi, J. Am. Chem. Soc. 2009, 131, 3430
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3430
-
-
Terada, M.1
Tanaka, H.2
Sorimachi, K.3
-
115
-
-
67749089286
-
-
M. Lu, D. Zhu, Y. Lu, X. Zeng, B. Tan, Z, Xu, G. Zhong, J. Am. Chem. Soc. 2009, 131, 4562
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 4562
-
-
Lu, M.1
Zhu, D.2
Lu, Y.3
Zeng, X.4
Tan, B.5
Xu, Z.6
Zhong, G.7
-
116
-
-
67649958204
-
-
Z.-Y. Han, H, Xiao, X.-H. Chen, L.-Z. Gong, J. Am. Chem. Soc. 2009, 131, 9182
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 9182
-
-
Han, Z.-Y.1
Xiao, H.2
Chen, X.-H.3
Gong, L.-Z.4
-
117
-
-
71949121949
-
-
T. Akiyama, T. Katoh, K. Mori, Angew. Chem. 2009, 121, 4290
-
(2009)
Angew. Chem.
, vol.121
, pp. 4290
-
-
Akiyama, T.1
Katoh, T.2
Mori, K.3
-
119
-
-
77749240146
-
-
K. Mori, T. Katoh, T. Suzuki, T. Noji, M. Yamanaka, T. Akiyama, Angew. Chem. 2009, 121, 9832-9834
-
(2009)
Angew. Chem.
, vol.121
, pp. 9832-9834
-
-
Mori, K.1
Katoh, T.2
Suzuki, T.3
Noji, T.4
Yamanaka, M.5
Akiyama, T.6
-
120
-
-
71949117515
-
-
Angew. Chem. Int. Ed. 2009, 48, 9652-9654
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9652-9654
-
-
-
121
-
-
77149176385
-
-
T. Yue, M.-X. Wang, D.-X. Wang, G. Masson, J. Zhu, Angew. Chem. 2009, 121, 6845
-
(2009)
Angew. Chem.
, vol.121
, pp. 6845
-
-
Yue, T.1
Wang, M.-X.2
Wang, D.-X.3
Masson, G.4
Zhu, J.5
-
123
-
-
77950200576
-
-
Q. Gu, Z.-Q. Rong, C. Zheng, S.-L. You, J. Am. Chem. Soc. 2010, 132, 4056
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4056
-
-
Gu, Q.1
Rong, Z.-Q.2
Zheng, C.3
You, S.-L.4
-
126
-
-
42749097242
-
-
V. Y. Korotaev, V. Y. Sosnovskikh, I. B. Kutyashev. A. Y. Barkov, E. G. Matochkina, M. Kodess, Tetrahedron 2008, 64, 5055.
-
(2008)
Tetrahedron
, vol.64
, pp. 5055
-
-
Korotaev, V.Y.1
Sosnovskikh, V.Y.2
Barkov, I.B.3
Kutyashev, A.Y.4
Matochkina, E.G.5
Kodess, M.6
-
127
-
-
0036353686
-
-
Y. Niwa, K. Takayama, M. Shimizu, Bull. Chem. Soc. Jpn. 2002, 75, 1819
-
(2002)
Bull. Chem. Soc. Jpn.
, vol.75
, pp. 1819
-
-
Niwa, Y.1
Takayama, K.2
Shimizu, M.3
-
128
-
-
53849146708
-
-
G.-W. Zhang, L. Wang, J. Nie, J.-A. Ma, Adv. Synth. Catal. 2008, 350, 1457.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1457
-
-
Zhang, G.-W.1
Wang, L.2
Nie, J.3
Ma, J.-A.4
-
129
-
-
33749522044
-
-
For a related transition state, see:, The phosphate oxygen could form an additional hydrogen bond with the NH group of Hantzsch ester leading to a ternary complex. Delivering the hydride in a pseudo-intramolecular fashion would then afford the same observed enantiomer, see
-
For a related transition state, see:, T. Akiyama, H. Morita, K. Fuchibe, J. Am. Chem. Soc. 2006, 128, 13070; The phosphate oxygen could form an additional hydrogen bond with the NH group of Hantzsch ester leading to a ternary complex. Delivering the hydride in a pseudo-intramolecular fashion would then afford the same observed enantiomer, see
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13070
-
-
Akiyama, T.1
Morita, H.2
Fuchibe, K.3
-
132
-
-
0036153865
-
-
for reviews, see
-
M. Gillard, C. van der Perren, N. Moguilevsky, R. Massingham, P. Chatelain, Mol. Pharmacol. 2002, 61, 391; for reviews, see
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 391
-
-
Gillard, M.1
Van Der Perren, C.2
Moguilevsky, N.3
Massingham, R.4
Chatelain, P.5
-
133
-
-
3042778690
-
-
J. H. Day, A. K. Ellis, E. Rafeiro, Drugs Today 2004, 40, 415
-
(2004)
Drugs Today
, vol.40
, pp. 415
-
-
Day, J.H.1
Ellis, A.K.2
Rafeiro, E.3
-
135
-
-
80051755049
-
-
For general reviews on carbonylation reactions, see
-
For general reviews on carbonylation reactions, see
-
-
-
-
136
-
-
77954786152
-
-
(Ed.: L. Kollár), Wiley-VCH, Weinheim
-
Modern Carbonylation Methods (Ed.:, L. Kollár,), Wiley-VCH, Weinheim, 2008
-
(2008)
Modern Carbonylation Methods
-
-
-
138
-
-
84855317746
-
-
A. Brennführer, H. Neumann, M. Beller, Angew. Chem. 2009, 121, 4176
-
(2009)
Angew. Chem.
, vol.121
, pp. 4176
-
-
Brennführer, A.1
Neumann, H.2
Beller, M.3
-
140
-
-
2442653750
-
-
X. Wu, A. K. Mahalingam, Y. Wan, M. Alterman, Tetrahedron Lett. 2004, 45, 4635.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4635
-
-
Wu, X.1
Mahalingam, A.K.2
Wan, Y.3
Alterman, M.4
-
141
-
-
80051718732
-
-
For recent syntheses based on Rh-catalyzed enantioselective arylations of arylimines with aryl boron reagents, see: Ref. [3g]
-
For recent syntheses based on Rh-catalyzed enantioselective arylations of arylimines with aryl boron reagents, see: Ref. [3g]
-
-
-
-
142
-
-
0034616722
-
-
for recent chiral-auxiliary-mediated asymmetric synthesis, see
-
for recent chiral-auxiliary-mediated asymmetric synthesis, see:, S. M. Allin, C. Northfield, M. I. Page, A. M. Z. Slawin, J. Chem. Soc. Perkin Trans. 1 2000, 1715
-
(2000)
J. Chem. Soc. Perkin Trans. 1
, pp. 1715
-
-
Allin, S.M.1
Northfield, C.2
Page, M.I.3
Slawin, A.M.Z.4
-
143
-
-
0041402770
-
-
E. Deniau, D. Enders, A. Couture, P. Drandclaudon, Tetrahedron: Asymmetry 2003, 14, 2253
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 2253
-
-
Deniau, E.1
Enders, D.2
Couture, A.3
Drandclaudon, P.4
-
144
-
-
12344317278
-
-
D. L. Comins, S. Schilling, Y. Zhang, Org. Lett. 2005, 7, 95
-
(2005)
Org. Lett.
, vol.7
, pp. 95
-
-
Comins, D.L.1
Schilling, S.2
Zhang, Y.3
-
145
-
-
13844294123
-
-
E. Deniau, D. Enders, A. Couture, P. Grandclaudon, Tetrahedron: Asymmetry 2005, 16, 875
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 875
-
-
Deniau, E.1
Enders, D.2
Couture, A.3
Grandclaudon, P.4
-
147
-
-
45549095602
-
-
X.-W. Sun, M. Liu, M.-H. Xu, G.-Q. Lin, Org. Lett. 2008, 10, 1259
-
(2008)
Org. Lett.
, vol.10
, pp. 1259
-
-
Sun, X.-W.1
Liu, M.2
Xu, M.-H.3
Lin, G.-Q.4
-
148
-
-
38349022144
-
-
M. Lamblin, A. Couture, E. Deniau, P. Grandclaudon, Tetrahedron: Asymmetry 2008, 19, 111
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 111
-
-
Lamblin, M.1
Couture, A.2
Deniau, E.3
Grandclaudon, P.4
-
149
-
-
58349112732
-
-
E. Deniau, A. Couture, P. Grandclaudon, Tetrahedron: Asymmetry 2008, 19, 2735; for a review, see
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 2735
-
-
Deniau, E.1
Couture, A.2
Grandclaudon, P.3
-
151
-
-
80051765900
-
-
N-Aryl substrates having o-Me or o-Cl instead of a o-OH group were inert under our standard conditions, see ref. [7b].
-
N-Aryl substrates having o-Me or o-Cl instead of a o-OH group were inert under our standard conditions, see ref. [7b].
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