-
2
-
-
84887856704
-
-
For details on a cost-efficient synthesis of the pyrazine moiety (R)- 3, see: (F. Hoffmann-La Roche AG). PCT Int. Appl. WO/2011/023706 A1
-
For details on a cost-efficient synthesis of the pyrazine moiety (R)- 3, see: Bachmann, S.; Fettes, A.;; Iding, H.; Wirz, B.; Zutter, U. (F. Hoffmann-La Roche AG). PCT Int. Appl. WO/2011/023706 A1, 2011.
-
(2011)
-
-
Bachmann, S.1
Fettes, A.2
Iding, H.3
Wirz, B.4
Zutter, U.5
-
3
-
-
0003445429
-
-
In, 1 st ed. (: Jacobsen, E. N. Pfaltz, A. Yamamoto, H.), Springer Verlag, Berlin, Chapter 3
-
Brown, J. M. In Comprehensive Asymmetric Catalysis, 1 st ed. (Eds.: Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H.), Springer Verlag, Berlin, 1999, Chapter 3.
-
(1999)
Comprehensive Asymmetric Catalysis
-
-
Brown, J.M.1
-
4
-
-
0034697497
-
-
For large-scale application of hydrogenation processes see: 1 st ed. Wiley-VCH Verlag, Weinheim, Chapters I.2-I.5 and III.2-III.3
-
For large-scale application of hydrogenation processes see: Asymmetric Catalysis on Industrial Scale, 1 st ed.; Blaser, H. U.; Schmidt, E., Eds.; Wiley-VCH Verlag, Weinheim, Chapters I.2-I.5 and III.2-III.3, 2004.
-
(2004)
Asymmetric Catalysis on Industrial Scale
-
-
Blaser, H.U.1
Schmidt, E.2
-
5
-
-
0038164344
-
-
Sturm, T.; Weissenstein, W.; Spindler, F. Adv. Synth. Catal. 2003, 345, 160
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 160
-
-
Sturm, T.1
Weissenstein, W.2
Spindler, F.3
-
6
-
-
22144490225
-
-
Cheng, X.; Zhang, Q.; Xie, J. H.; Wang, L. X.; Zhou, Q.-L. Angew. Chem. 2005, 117, 1142
-
(2005)
Angew. Chem.
, vol.117
, pp. 1142
-
-
Cheng, X.1
Zhang, Q.2
Xie, J.H.3
Wang, L.X.4
Zhou, Q.-L.5
-
8
-
-
48049097925
-
-
Chen, W.; McCormack, P. J.; Mohammed, K.; Mbafor, W.; Roberts, S. M.; Whittall, J. Angew. Chem. 2007, 119, 4219
-
(2007)
Angew. Chem.
, vol.119
, pp. 4219
-
-
Chen, W.1
McCormack, P.J.2
Mohammed, K.3
Mbafor, W.4
Roberts, S.M.5
Whittall, J.6
-
10
-
-
38849134221
-
-
Fox, M. E.; Jackson, M.; Lennon, I. C.; Klosin, J.; Abboud, K. A. J. Org. Chem. 2008, 73, 775
-
(2008)
J. Org. Chem.
, vol.73
, pp. 775
-
-
Fox, M.E.1
Jackson, M.2
Lennon, I.C.3
Klosin, J.4
Abboud, K.A.5
-
11
-
-
49049096215
-
-
Wassenaar, J.; Kuil, M.; Reek, J. N. H. Adv. Synth. Catal. 2008, 350, 1610
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1610
-
-
Wassenaar, J.1
Kuil, M.2
Reek, J.N.H.3
-
12
-
-
38349141018
-
-
Fukuzawa, S.-I.; Oki, H.; Hosaka, M.; Sugasawa, J.; Kikuchi, S. Org. Lett. 2007, 9, 5557
-
(2007)
Org. Lett.
, vol.9
, pp. 5557
-
-
Fukuzawa, S.-I.1
Oki, H.2
Hosaka, M.3
Sugasawa, J.4
Kikuchi, S.5
-
13
-
-
56749091751
-
-
Szollosi, G.; Herman, B.; Felföldi, K.; Fülöp, F.; Bartok, M. Adv. Synth. Catal. 2008, 350, 2804
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2804
-
-
Szollosi, G.1
Herman, B.2
Felföldi, K.3
Fülöp, F.4
Bartok, M.5
-
14
-
-
84861679612
-
-
Yang, S.; Zhu, S.-F.; Zhang, C.-M.; Song, S.; Yu, Y.-B.; Li, S.; Zhou, Q.-L. Tetrahedron 2012, 68, 5172
-
(2012)
Tetrahedron
, vol.68
, pp. 5172
-
-
Yang, S.1
Zhu, S.-F.2
Zhang, C.-M.3
Song, S.4
Yu, Y.-B.5
Li, S.6
Zhou, Q.-L.7
-
16
-
-
24944457661
-
-
Hoen, R.; Boogers, J. A. F.; Bernsmann, H.; Minnaard, A. J.; Meetsma, A.; Tiemersma-Wegman, T. D.; de Vries, A. H. M.; de Vries, J. G.; Feringa, B. L. Angew. Chem. 2005, 117, 4281
-
(2005)
Angew. Chem.
, vol.117
, pp. 4281
-
-
Hoen, R.1
Boogers, J.A.F.2
Bernsmann, H.3
Minnaard, A.J.4
Meetsma, A.5
Tiemersma-Wegman, T.D.6
De Vries, A.H.M.7
De Vries, J.G.8
Feringa, B.L.9
-
18
-
-
34548178516
-
-
Moberg, V.; Haukka, M.; Koshevoy, I. O.; Ortiz, R.; Nordlander, E. Organometallics 2007, 26, 4090
-
(2007)
Organometallics
, vol.26
, pp. 4090
-
-
Moberg, V.1
Haukka, M.2
Koshevoy, I.O.3
Ortiz, R.4
Nordlander, E.5
-
19
-
-
46949106771
-
-
Li, S.; Zhu, S.-F.; Zhang, C.-M.; Song, S.; Zhou, Q.-L. J. Am. Chem. Soc. 2008, 130, 8584
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 8584
-
-
Li, S.1
Zhu, S.-F.2
Zhang, C.-M.3
Song, S.4
Zhou, Q.-L.5
-
20
-
-
63549131999
-
-
Espino, G.; Xiao, L.; Puchberger, M.; Mereiter, K.; Spindler, F.; Manzano, B. R.; Jalon, F. A.; Weissensteiner, W. Dalton Trans. 2009, 2751
-
(2009)
Dalton Trans.
, pp. 2751
-
-
Espino, G.1
Xiao, L.2
Puchberger, M.3
Mereiter, K.4
Spindler, F.5
Manzano, B.R.6
Jalon, F.A.7
Weissensteiner, W.8
-
21
-
-
84861795087
-
-
Rageot, D.; Woodmansee, D. H.; Pugin, B.; Pflatz, A. Angew. Chem. 2011, 123, 9772
-
(2011)
Angew. Chem.
, vol.123
, pp. 9772
-
-
Rageot, D.1
Woodmansee, D.H.2
Pugin, B.3
Pflatz, A.4
-
23
-
-
47749124955
-
-
Bertram, L. S.; Black, D.; Briner, P. H.; Chatfield, R.; Cooke, A.; Fyfe, M. C. T.; Murray, P. J.; Naud, F.; Nawano, M.; Procter, M. J.; Rakipovski, G.; Rasamison, C. M.; Raynet, C.; Schofield, K. L.; Shah, V. K.; Spindler, F.; Taylor, A.; Turton, R.; Williams, G. M.; Wong-Kai-In, P.; Yasuda, K. J. Med. Chem. 2008, 51, 4340
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4340
-
-
Bertram, L.S.1
Black, D.2
Briner, P.H.3
Chatfield, R.4
Cooke, A.5
Fyfe, M.C.T.6
Murray, P.J.7
Naud, F.8
Nawano, M.9
Procter, M.J.10
Rakipovski, G.11
Rasamison, C.M.12
Raynet, C.13
Schofield, K.L.14
Shah, V.K.15
Spindler, F.16
Taylor, A.17
Turton, R.18
Williams, G.M.19
Wong-Kai-In, P.20
Yasuda, K.21
more..
-
24
-
-
84887972247
-
-
WO/2006/016178 A1
-
Briner, P. H.; Fyfe, M. C. T.; Madeley, J. P.; Murray, P. J.; Procter, M. J.; Spindler, F. WO/2006/016178 A1, 2006
-
(2006)
-
-
Briner, P.H.1
Fyfe, M.C.T.2
Madeley, J.P.3
Murray, P.J.4
Procter, M.J.5
Spindler, F.6
-
25
-
-
84862076975
-
-
Magnus, N. A.; Braden, T. M.; Buser, J. Y.; De Baillie, A. C.; Heath, P. C.; Ley, C. P.; Remacle, J. R.; Varies, D. L.; Wilson, T. M. Org. Process Res. Dev. 2012, 16, 830
-
(2012)
Org. Process Res. Dev.
, vol.16
, pp. 830
-
-
Magnus, N.A.1
Braden, T.M.2
Buser, J.Y.3
De Baillie, A.C.4
Heath, P.C.5
Ley, C.P.6
Remacle, J.R.7
Varies, D.L.8
Wilson, T.M.9
-
26
-
-
72149116472
-
-
Zhang, Y.; Han, Z.; Ding, K.; Zhang, A. Chem. Commun. 2010, 46, 156
-
(2010)
Chem. Commun.
, vol.46
, pp. 156
-
-
Zhang, Y.1
Han, Z.2
Ding, K.3
Zhang, A.4
-
27
-
-
84872840332
-
-
Zhu, S.-F.; Yu, Y.-B.; Li, S.; Wang, L.-X.; Zhou, Q.-L. Angew. Chem. 2012, 124, 9002
-
(2012)
Angew. Chem.
, vol.124
, pp. 9002
-
-
Zhu, S.-F.1
Yu, Y.-B.2
Li, S.3
Wang, L.-X.4
Zhou, Q.-L.5
-
29
-
-
84873337879
-
-
During the preparation of this manuscript a review appeared which assesses the state of the art in the asymmetric hydrogenation of variously substituted acrylic substrates
-
During the preparation of this manuscript a review appeared which assesses the state of the art in the asymmetric hydrogenation of variously substituted acrylic substrates: Khumsubdee, S.; Burgess, K. ACS Catal. 2013, 3, 237
-
(2013)
ACS Catal.
, vol.3
, pp. 237
-
-
Khumsubdee, S.1
Burgess, K.2
-
31
-
-
33746923435
-
-
For a review, see
-
For a review, see: Caron, S.; Dugger, R. W.; Ruggeri, S. G.; Ragan, J. A.; Brown Ripin, D. H. Chem. Rev. 2006, 106, 2943
-
(2006)
Chem. Rev.
, vol.106
, pp. 2943
-
-
Caron, S.1
Dugger, R.W.2
Ruggeri, S.G.3
Ragan, J.A.4
Brown Ripin, D.H.5
-
32
-
-
0033532012
-
-
Zhao, D.; Xu, F.; Chen, C.-Y.; Tillyer, R. D.; Grabowski, E. I. J.; Reider, P. J. Tetrahedron 1999, 55, 6001
-
(1999)
Tetrahedron
, vol.55
, pp. 6001
-
-
Zhao, D.1
Xu, F.2
Chen, C.-Y.3
Tillyer, R.D.4
Grabowski, E.I.J.5
Reider, P.J.6
-
35
-
-
34547856209
-
-
Brown Ripin, D. H.; Weisenburger, G. A.; am Ende, D. J.; Bill, D. R.; Clifford, P. J.; Meltz, C. N.; Phillips, J. E. Org. Process Res. Dev. 2007, 11, 762
-
(2007)
Org. Process Res. Dev.
, vol.11
, pp. 762
-
-
Brown Ripin, D.H.1
Weisenburger, G.A.2
Am Ende, D.J.3
Bill, D.R.4
Clifford, P.J.5
Meltz, C.N.6
Phillips, J.E.7
-
37
-
-
84861679612
-
-
The Ir-SIPHOX catalysts have been proven to be highly enantioselective catalysts in the asymmetric hydrogenation of α-alkyl β-aryl (see reference 6d) and α β-diaryl acrylic acid derivatives. See
-
The Ir-SIPHOX catalysts have been proven to be highly enantioselective catalysts in the asymmetric hydrogenation of α-alkyl β-aryl (see reference 6d) and α,β-diaryl acrylic acid derivatives. See: Yang, S.; Zhu, S.-F.; Zhang, C.-M.; Song, S.; Yu, Y.-B.; Li, S.; Zhou, Q.-L. Tetrahedron 2012, 68, 5172
-
(2012)
Tetrahedron
, vol.68
, pp. 5172
-
-
Yang, S.1
Zhu, S.-F.2
Zhang, C.-M.3
Song, S.4
Yu, Y.-B.5
Li, S.6
Zhou, Q.-L.7
-
38
-
-
0037425538
-
-
A similar pressure dependency on the activity of Ir catalysts has already been described
-
A similar pressure dependency on the activity of Ir catalysts has already been described: Perry, M. C.; Cui, X.; Powell, M. T.; Hou, D.-R.; Reibenspies, J. H.; Burgess, K. J. Am. Chem. Soc. 2003, 125, 113
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 113
-
-
Perry, M.C.1
Cui, X.2
Powell, M.T.3
Hou, D.-R.4
Reibenspies, J.H.5
Burgess, K.6
-
39
-
-
76249120326
-
-
For the syntheses of Ru-Mandyphos and Ru-Taniaphos complexes see: In; Prunier, M. L. CRC Press, London, Chapter 23, Ferrocene-derived ligands are commercially available from Solvias AG; a variety of defined Ru-ferrocene complexes such as 13 are available from Umicore AG
-
For the syntheses of Ru-Mandyphos and Ru-Taniaphos complexes see: Briel, O.; Doppiu, A.; Karch, R.; Le Ret, C.; Winde, R.; Rivas Nass, A. In Catalysis of Organic Reactions; Prunier, M. L., Ed.; CRC Press, London, Chapter 23, 2009. Ferrocene-derived ligands are commercially available from Solvias AG; a variety of defined Ru-ferrocene complexes such as 13 are available from Umicore AG.
-
(2009)
Catalysis of Organic Reactions
-
-
Briel, O.1
Doppiu, A.2
Karch, R.3
Le Ret, C.4
Winde, R.5
Rivas Nass, A.6
-
40
-
-
84887881711
-
-
The EMEA guideline EMEA/CHMP/SWP/4446/2000 defines the highest contents of various metals in the API
-
The EMEA guideline EMEA/CHMP/SWP/4446/2000 defines the highest contents of various metals in the API: http://www.ema.europa.eu/docs/en-GB/document- library/Scientific-guideline/2009/09/WC500003586.pdf.
-
-
-
-
41
-
-
84866927400
-
-
An alternative preparation and full characterization of (R)- 2 can be found in
-
An alternative preparation and full characterization of (R)- 2 can be found in: Sarabu, R.; Bizzarro, F. T.; Corbett, W. L.; Dvorozniak, M. T.; Geng, W.; Grippo, J. F.; Haynes, N.-E.; Hutchings, S.; Garfalo, L.; Guetin, K. R.; Hilliard, D. W.; Kabat, M.; Kester, R. F.; Ka, W.; Liang, Z.; Mahaney, P. E.; Marcus, L.; Matschinsky, F. M.; Moore, D.; Racha, J.; Radinov, R.; Ren, Y.; Qi, L.; Pignatello, M.; Spence, C. L.; Steele, T.; Tengi, J.; Grimsby, J. J. Med. Chem. 2012, 55, 7021
-
(2012)
J. Med. Chem.
, vol.55
, pp. 7021
-
-
Sarabu, R.1
Bizzarro, F.T.2
Corbett, W.L.3
Dvorozniak, M.T.4
Geng, W.5
Grippo, J.F.6
Haynes, N.-E.7
Hutchings, S.8
Garfalo, L.9
Guetin, K.R.10
Hilliard, D.W.11
Kabat, M.12
Kester, R.F.13
Ka, W.14
Liang, Z.15
Mahaney, P.E.16
Marcus, L.17
Matschinsky, F.M.18
Moore, D.19
Racha, J.20
Radinov, R.21
Ren, Y.22
Qi, L.23
Pignatello, M.24
Spence, C.L.25
Steele, T.26
Tengi, J.27
Grimsby, J.28
more..
|