-
2
-
-
0027751835
-
-
(b) Spencer, C. M.; Foulds, D.; Peters, D. H. Drugs 1993, 46, 1055.
-
(1993)
Drugs
, vol.46
, pp. 1055
-
-
Spencer, C.M.1
Foulds, D.2
Peters, D.H.3
-
3
-
-
0029963205
-
-
Patent applications include
-
(c) Sakurai, S.; Ogawa, N.; Suzuki, T.; Kato, K.; Ohashi, T.; Yasuda, S.; Kato, H.; Ito, Y. Chem. Pharm. Bull. 1996, 44, 765. Patent applications include:
-
(1996)
Chem. Pharm. Bull.
, vol.44
, pp. 765
-
-
Sakurai, S.1
Ogawa, N.2
Suzuki, T.3
Kato, K.4
Ohashi, T.5
Yasuda, S.6
Kato, H.7
Ito, Y.8
-
4
-
-
77950794979
-
-
WO 01/ 07050 A1 (Schering-Plough).
-
(d) Tulshian, D.; Ho, G. D.; Silverman, L.; Matasi, J. J.; McLeod, R. L.; Hey, J. A.; Chapman, R. W.; Bercovici, A.; Cuss, F. M. WO 01/ 07050 A1 (Schering-Plough).
-
-
-
Tulshian, D.1
Ho, G.D.2
Silverman, L.3
Matasi, J.J.4
McLeod, R.L.5
Hey, J.A.6
Chapman, R.W.7
Bercovici, A.8
Cuss, F.M.9
-
7
-
-
77950823425
-
-
WO 2007/062193 A1 (Merck). Cetirizine·HCl, a histamine H1-receptor inverse agonist is commercialized as Zyrtec/Reactine by Pfizer.
-
(g) Baker, R. K; Hale, J. J.; Maio, S.; Rupprecht, K. M. WO 2007/062193 A1 (Merck). Cetirizine·HCl, a histamine H1-receptor inverse agonist is commercialized as Zyrtec/Reactine by Pfizer.
-
-
-
Baker, R.K.1
Hale, J.J.2
Maio, S.3
Rupprecht, K.M.4
-
8
-
-
0025144699
-
-
(a) Tomioka, K.; Inoue, I.; Shindo, M.; Koga, K. Tetrahedron Lett. 1990, 31, 6681.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 6681
-
-
Tomioka, K.1
Inoue, I.2
Shindo, M.3
Koga, K.4
-
9
-
-
0001767983
-
-
(b) Pridgen, L. N.; Mokhallalati, M. K.; Wu, M. J. J. Org. Chem. 1992, 57, 1237.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 1237
-
-
Pridgen, L.N.1
Mokhallalati, M.K.2
Wu, M.J.3
-
10
-
-
0032573617
-
-
(c) Delorme, D.; Berthelette, C.; Lavoie, R.; Roberts, E. Tetrahedron: Asymmetry 1998, 9, 3963.
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 3963
-
-
Delorme, D.1
Berthelette, C.2
Lavoie, R.3
Roberts, E.4
-
12
-
-
0037016979
-
-
(e) Pflum, D. A.; Krishnamurthy, D.; Han, Z.; Wald, S. A.; Senanayake, C. H. 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
-
13
-
-
2442676282
-
-
(f) Cabello, N.; Kizirian, J.-C.; Alexakis, Tetrahedron Lett. 2004, 45, 4639.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4639
-
-
Cabello, N.1
Kizirian, J.-C.2
Alexakis, A.3
-
14
-
-
13644262210
-
-
(g) Weix, D. J.; Shi, Y.; Ellman, J. A. J. Am. Chem. Soc. 2005, 127, 1092.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 1092
-
-
Weix, D.J.1
Shi, Y.2
Ellman, J.A.3
-
16
-
-
0034624432
-
-
Rh-catalyzed enantioselective additions of arylstannanes: (a) Aryltitaniums
-
Rh-catalyzed enantioselective additions of arylstannanes: (a) Hayashi, T.; Ishigedani, M. J. Am. Chem. Soc. 2000, 122, 976. Aryltitaniums:
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 976
-
-
Hayashi, T.1
Ishigedani, M.2
-
17
-
-
10044235122
-
-
Arylboronic acids
-
(b) Hayashi, T.; Kawai, M.; Tokunaga, N. Angew. Chem. Int. Ed. 2004, 43, 6125. Arylboronic acids:
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6125
-
-
Hayashi, T.1
Kawai, M.2
Tokunaga, N.3
-
18
-
-
3042817456
-
-
(c) Kuriyama, M.; Soeta, T.; Hao, X.; Chen, Q.; Tomioka, K. 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
-
19
-
-
33745541260
-
-
(d) Duan, H.-F.; Jia, Y.-X.; Wang, L.-X.; Zhou, Q.-L. 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
-
20
-
-
33745577878
-
-
(e) Jagt, R. B. C.; Toullec, P. Y.; Geerdink, D.; de Vries, J. G.; Feringa, B. L.; Minnaard, A. J. Angew. Chem. Int. Ed. 2006, 45, 2789.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 2789
-
-
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
-
21
-
-
34247897083
-
-
Also see ref 2g.
-
(f) Wang, Z.-Q.; Feng, C.-G.; Xu, M.-H.; Lin, G.-Q. J. Am. Chem. Soc. 2007, 129, 5336. Also see ref 2g.
-
(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
-
22
-
-
0037020423
-
-
2Zn to N-formyl imines has also been reported. See
-
2Zn to N-formyl imines has also been reported. See: Hermanns, N.; Dahmen, S.; Bolm, C.; Bräse, S. Angew. Chem. Int. Ed 2002, 41, 3692.
-
(2002)
Angew. Chem. Int. Ed
, vol.41
, pp. 3692
-
-
Hermanns, N.1
Dahmen, S.2
Bolm, C.3
Bräse, S.4
-
23
-
-
34250891292
-
-
Clayden, J.; Dufour, J.; Grainger, D. M.; Helliwell, M. J. Am. Chem. Soc. 2007, 129, 7488.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 7488
-
-
Clayden, J.1
Dufour, J.2
Grainger, D.M.3
Helliwell, M.4
-
24
-
-
0030575358
-
-
3 complex followed by nucleophilic displacement, see
-
3 complex followed by nucleophilic displacement, see: Corey, E. J.; Helal, C. J. Tetrahedron Lett. 1996, 37, 4837.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4837
-
-
Corey, E.J.1
Helal, C.J.2
-
25
-
-
0001286347
-
-
(a) Ohkuma, T.; Koizumi, M.; Ikehira, H.; Yokozawa, T.; Noyori, R. Org. Lett. 2000, 2, 659.
-
(2000)
Org. Lett.
, vol.2
, pp. 659
-
-
Ohkuma, T.1
Koizumi, M.2
Ikehira, H.3
Yokozawa, T.4
Noyori, R.5
-
26
-
-
0346025400
-
-
(b) Chen, C.-y.; Reamer, R. A.; Chilenski, J. R.; McWilliams, C. J. Org. Lett. 2003, 5, 5039.
-
(2003)
Org. Lett.
, vol.5
, pp. 5039
-
-
Chen, C.-Y.1
Reamer, R.A.2
Chilenski, J.R.3
McWilliams, C.J.4
-
27
-
-
77950817438
-
-
Patent WO 01/040162 A1, (Takeda Chemical Industries).
-
(c) Yamano, T.; Oi, S.; Yamashita, M. Patent WO 01/040162 A1, 2001 (Takeda Chemical Industries).
-
(2001)
-
-
Yamano, T.1
Oi, S.2
Yamashita, M.3
-
32
-
-
0043240879
-
-
For reviews, see: (a)
-
For reviews, see: (a) Tang, W.; Zhang, X. Chem. Rev. 2003, 103, 3029.
-
(2003)
Chem. Rev.
, vol.103
, pp. 3029
-
-
Tang, W.1
Zhang, X.2
-
34
-
-
84890985460
-
-
de Vries, J. G., Elsevier, C. J., Eds.; Wiley-VCH: Weinheim, Germany
-
(c) Handbook of Homogeneous Hydrogenation; de Vries, J. G., Elsevier, C. J., Eds.; Wiley-VCH: Weinheim, Germany, 2007.
-
(2007)
Handbook of Homogeneous Hydrogenation
-
-
-
35
-
-
67651211401
-
-
Hou, G.; Gosselin, F.; Li, W.; McWilliams, C. J.; Sun, Y.; O'Shea, P. D.; Davies, I. W.; Chen, C.-y.; Zhang, X. 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, C.J.4
Sun, Y.5
O'Shea, P.D.6
Davies, I.W.7
Chen, C.-Y.8
Zhang, X.9
-
36
-
-
1542345321
-
-
For a Pd-catalyzed C-H activation approach, see: (a)
-
For a Pd-catalyzed C-H activation approach, see: (a) Zhou, C.; Larock, R. C. J. Am. Chem. Soc. 2004, 126, 2302.
-
(2004)
C. J. Am. Chem. Soc.
, vol.126
, pp. 2302
-
-
Zhou, C.1
Larock, R.2
-
38
-
-
84857445436
-
-
2 to benzophenones, see
-
2 to benzophenones, see: Kruger, C.; Rochow, E.; Wanagat, U. Chem. Ber. 1963, 96, 2132.
-
(1963)
Chem. Ber.
, vol.96
, pp. 2132
-
-
Kruger, C.1
Rochow, E.2
Wanagat, U.3
-
39
-
-
0037065328
-
-
ForRh-catalyzed asymmetric hydrogenation of protected β-dehydroamino esters using ligand 4, see
-
ForRh-catalyzed asymmetric hydrogenation of protected β-dehydroamino esters using ligand 4, see: Peña, D.; Minnaard, A. J.; de Vries, J. G.; Feringa, B. L. J. Am. Chem. Soc. 2002, 124, 14552.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 14552
-
-
Peña, D.1
Minnaard, A.J.2
De Vries, J.G.3
Feringa, B.L.4
-
40
-
-
38049033351
-
-
(a) Minnaard, A. J.; Feringa, B. L.; Lefort, L.; de Vries, J. G. Acc. Chem. Res. 2007, 40, 1267.
-
(2007)
Acc. Chem. Res.
, vol.40
, pp. 1267
-
-
Minnaard, A.J.1
Feringa, B.L.2
Lefort, L.3
De Vries, J.G.4
-
41
-
-
2942599460
-
-
(b) Lefort, L.; Boogers, J. A. F.; Minnaard, A. J.; Feringa, B. L.; de Vries, J. G. Org. Lett. 2004, 6, 1733.
-
(2004)
Org. Lett.
, vol.6
, pp. 1733
-
-
Lefort, L.1
Boogers, J.A.F.2
Minnaard, A.J.3
Feringa, B.L.4
De Vries, J.G.5
-
42
-
-
67650532877
-
-
Mršić, N.; Minnaard, A. J.; Feringa, B. L.; de Vries, J. G. J. Am. Chem. Soc. 2009, 131, 8358.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 8358
-
-
Mršić, N.1
Minnaard, A.J.2
Feringa, B.L.3
De Vries, J.G.4
-
43
-
-
34247892462
-
-
Inferior results were obtained with, metal/ligand ratios of 1:1 (76% conv, 56% ee) and 1:3 (11% conv, 41% ee) using imine la. Single monodentate phosphoramidite-iridium complexes can afford high enantioselectivities; see: Giacomina, F.; Meetsma, A.; Panella, L.; Lefort, L.; de Vries, A. H. M.; de Vries, J. G. Angew. Chem. Int. Ed. 2007, 46, 1497.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1497
-
-
Giacomina, F.1
Meetsma, A.2
Panella, L.3
Lefort, L.4
De Vries, A.H.M.5
De Vries, J.G.6
-
44
-
-
53949112678
-
-
Chloride additives improve the enantioselectivity in Ir-phosphoramidite- catalyzed hydrogenations of quinolines. See: Mršić, N.; Lefort, L.; Boogers, J. A. F.; Minnaard, A. J.; Feringa, B. L.; de Vries, J. G. Adv. Synth. Catal. 2008, 350, 1081.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1081
-
-
Mršić, N.1
Lefort, L.2
Boogers, J.A.F.3
Minnaard, A.J.4
Feringa, B.L.5
De Vries, J.G.6
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