-
2
-
-
77954786152
-
-
C. Claver, C. Godard, A. Ruiz, O. Pmies, and M. Diéguez L. Kollár, Modern Carbonylation Methods 2008 Wiley-VCH Weinheim Chapter 3
-
(2008)
Modern Carbonylation Methods
-
-
Claver, C.1
Godard, C.2
Ruiz, A.3
Pmies, O.4
Diéguez, M.5
-
4
-
-
84891580093
-
Catalytic Asymmetric Synthesis
-
C. Godard, A. Ruiz, M. Diéguez, O. Pmies, and C. Claver I. Ojima, Catalytic Asymmetric Synthesis New Jersey 2010 Wiley 799 Chapter 10
-
(2010)
New Jersey
, pp. 799
-
-
Godard, C.1
Ruiz, A.2
Diéguez, M.3
Pmies, O.4
Claver, C.5
-
8
-
-
0004147148
-
-
P.W.N.M. van Leeuwen, C. Claver, Kluwer Academic Press Dordrecht
-
P.W.N.M. van Leeuwen, C. Claver, Rhodium Catalysed Hydroformylation 2000 Kluwer Academic Press Dordrecht
-
(2000)
Rhodium Catalysed Hydroformylation
-
-
-
10
-
-
24944547484
-
-
See for example: A.T. Axtell, C.J. Cobley, J. Klosin, G.T. Whiteker, A. Zanotti-Gerosa, and K.A. Abboud Angew. Chem., Int. Ed. 44 2005 5834
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 5834
-
-
Axtell, A.T.1
Cobley, C.J.2
Klosin, J.3
Whiteker, G.T.4
Zanotti-Gerosa, A.5
Abboud, K.A.6
-
11
-
-
26444560105
-
-
J. Huang, E. Bunel, A. Allgeier, J. Tedrow, T. Storz, J. Preston, T. Correll, D. Manley, T. Soukup, R. Jensen, R. Syed, G. Moniz, R. Larsen, M. Martinelli, and P.J. Reider Tetrahedron Lett. 46 2005 7831
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 7831
-
-
Huang, J.1
Bunel, E.2
Allgeier, A.3
Tedrow, J.4
Storz, T.5
Preston, J.6
Correll, T.7
Manley, D.8
Soukup, T.9
Jensen, R.10
Syed, R.11
Moniz, G.12
Larsen, R.13
Martinelli, M.14
Reider, P.J.15
-
12
-
-
17144407219
-
-
See for instance: T.P. Clark, C.R. Landis, S.L. Freed, J. Klosin, and K.A. Abboud J. Am. Chem. Soc. 127 2005 5040
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 5040
-
-
Clark, T.P.1
Landis, C.R.2
Freed, S.L.3
Klosin, J.4
Abboud, K.A.5
-
13
-
-
34547423389
-
-
P.J. Thomas, A.T. Axtell, J. Klosin, W. Peng, C.L. Rand, T.P. Clark, C.R. Landis, and K.A. Abboud Org. Lett. 9 2007 2665
-
(2007)
Org. Lett.
, vol.9
, pp. 2665
-
-
Thomas, P.J.1
Axtell, A.T.2
Klosin, J.3
Peng, W.4
Rand, C.L.5
Clark, T.P.6
Landis, C.R.7
Abboud, K.A.8
-
14
-
-
0034680632
-
-
S. Breeden, D.J. Cole-Hamilton, D.F. Foster, G.J. Schwarz, and M. Wills Angew. Chem., Int. Ed. 39 2000 4106
-
(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 4106
-
-
Breeden, S.1
Cole-Hamilton, D.J.2
Foster, D.F.3
Schwarz, G.J.4
Wills, M.5
-
18
-
-
0041495679
-
-
D. Peña, A.J. Minnaard, J.A. Boogers, A.H.M. de Vries, J.G. de Vries, and B.L. Feringa Org. Biomol. Chem. 1 2003 1087
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 1087
-
-
Peña, D.1
Minnaard, A.J.2
Boogers, J.A.3
De Vries, A.H.M.4
De Vries, J.G.5
Feringa, B.L.6
-
19
-
-
17644399859
-
-
See for instance: K. Biswas, O. Prieto, P.J. Goldsmith, and S. Woodward Angew. Chem., Int. Ed. 44 2005 2232
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 2232
-
-
Biswas, K.1
Prieto, O.2
Goldsmith, P.J.3
Woodward, S.4
-
21
-
-
35048898027
-
-
See for instance: L. Palais, I.S. Mikhel, C. Bournaud, L. Micouin, C.A. Falciola, M. Vuagnoux-d'Augustin, S. Rosset, G. Bernardinelli, and A. Alexakis Angew. Chem., Int. Ed. 46 2007 7462
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7462
-
-
Palais, L.1
Mikhel, I.S.2
Bournaud, C.3
Micouin, L.4
Falciola, C.A.5
Vuagnoux-D'Augustin, M.6
Rosset, S.7
Bernardinelli, G.8
Alexakis, A.9
-
23
-
-
51049122142
-
-
For a recent review on this topic, see also: A. Alexakis, J.E. Bäckvall, N. Krause, O. Pmies, and M. Diéguez Chem. Rev. 108 2008 2796
-
(2008)
Chem. Rev.
, vol.108
, pp. 2796
-
-
Alexakis, A.1
Bäckvall, J.E.2
Krause, N.3
Pmies, O.4
Diéguez, M.5
-
25
-
-
4644234208
-
-
It should be pointed out that related monophosphite ligands provided lower enantioselectivities (up to 43%) in the Rh-catalyzed hydroformylation of allyl cyanide. See: C.J. Cobley, J. Klosin, C. Qin, and G.T. Whiteker Org. Lett. 6 2004 3277
-
(2004)
Org. Lett.
, vol.6
, pp. 3277
-
-
Cobley, C.J.1
Klosin, J.2
Qin, C.3
Whiteker, G.T.4
-
26
-
-
2942536231
-
-
C.J. Cobley, K. Gardner, J. Klosin, C. Praquin, C. Hill, G.T. Whiteker, A. Zannotti-Gerosa, J.L. Petersen, and K. Abboud J. Org. Chem. 69 2004 4031
-
(2004)
J. Org. Chem.
, vol.69
, pp. 4031
-
-
Cobley, C.J.1
Gardner, K.2
Klosin, J.3
Praquin, C.4
Hill, C.5
Whiteker, G.T.6
Zannotti-Gerosa, A.7
Petersen, J.L.8
Abboud, K.9
-
29
-
-
20444390269
-
Phosphite Ligands in Asymmetric Hydrogenation
-
M. Diéguez, O. Pmies, A. Ruiz, and C. Claver Phosphite Ligands in Asymmetric Hydrogenation S.V. Malhotra, Methodologies in Asymmetric Catalysis Vol. 880 2004 ACS Washington 161
-
(2004)
Methodologies in Asymmetric Catalysis
, vol.880
, pp. 161
-
-
Diéguez, M.1
Pmies, O.2
Ruiz, A.3
Claver, C.4
-
31
-
-
43549107348
-
-
B.H.G. Swennenhuis, R. Chen, P.W.N.M. van Leeuwen, J.G. de Vries, and P.C.J. Kamer Org. Lett. 10 2008 989
-
(2008)
Org. Lett.
, vol.10
, pp. 989
-
-
Swennenhuis, B.H.G.1
Chen, R.2
Van Leeuwen, P.W.N.M.3
De Vries, J.G.4
Kamer, P.C.J.5
-
32
-
-
0037450022
-
-
See for instance: M.T. Reetz, T. Sell, A. Meiswinkel, and G. Mehler Angew. Chem., Int. Ed. 42 2003 790
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 790
-
-
Reetz, M.T.1
Sell, T.2
Meiswinkel, A.3
Mehler, G.4
-
34
-
-
77956189319
-
-
See for instance U.S. Patent 43,76,208
-
See for instance: Vietti, D. E. U.S. Patent 43,76,208, 1983
-
(1983)
-
-
Vietti, D.E.1
-
35
-
-
0000154238
-
-
T. Hoiuchi, T. Ota, E. Shirakawa, K. Nozaki, and H. Takaya J. Org. Chem 62 1997 4285
-
(1997)
J. Org. Chem
, vol.62
, pp. 4285
-
-
Hoiuchi, T.1
Ota, T.2
Shirakawa, E.3
Nozaki, K.4
Takaya, H.5
-
40
-
-
76349119025
-
-
S.H. Chikkali, R. Bellini, B. Berthon-Gelloz, J.I. van der Vlugt, B. de Bruin, and J.N.H. Reek Chem. Commun. 46 2010 1244
-
(2010)
Chem. Commun.
, vol.46
, pp. 1244
-
-
Chikkali, S.H.1
Bellini, R.2
Berthon-Gelloz, B.3
Van Der Vlugt, J.I.4
De Bruin, B.5
Reek, J.N.H.6
-
41
-
-
37049085654
-
-
A. Polo, J. Real, C. Claver, S. Castillón, and J.C. Bayón J. Chem. Soc., Chem. Commun. 1990 600
-
(1990)
J. Chem. Soc., Chem. Commun.
, pp. 600
-
-
Polo, A.1
Real, J.2
Claver, C.3
Castillón, S.4
Bayón, J.C.5
-
42
-
-
0000323153
-
-
A. Polo, C. Claver, S. Castillón, A. Ruiz, J.C. Bayón, J. Real, C. Mealli, and D. Masi Organometallics 11 1992 3525
-
(1992)
Organometallics
, vol.11
, pp. 3525
-
-
Polo, A.1
Claver, C.2
Castillón, S.3
Ruiz, A.4
Bayón, J.C.5
Real, J.6
Mealli, C.7
Masi, D.8
-
43
-
-
77956187793
-
-
There are only two Rh-catalytic systems that have provided better enantioselectivities. One modified with the phosphine-phosphite binaphos ligand (ees up to 76% and 69% for S8 and S9, respectively, see Ref. 14b) and the second modified with a furanoside diphosphite ligand (ees up to 68%, see Ref. 14e)
-
There are only two Rh-catalytic systems that have provided better enantioselectivities. One modified with the phosphine-phosphite binaphos ligand (ees up to 76% and 69% for S8 and S9, respectively, see Ref. 14b) and the second modified with a furanoside diphosphite ligand (ees up to 68%, see Ref. 14e).
-
-
-
-
47
-
-
0035898306
-
-
M. Diéguez, O. Pmies, A. Ruiz, S. Castillón, and C. Claver Chem. Eur. J. 7 2001 3086
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 3086
-
-
Diéguez, M.1
Pmies, O.2
Ruiz, A.3
Castillón, S.4
Claver, C.5
-
48
-
-
14544278529
-
-
E. Guimet, J. Parada, A. Ruiz, C. Claver, and M. Diéguez APCATA 282 2005 215
-
(2005)
APCATA
, vol.282
, pp. 215
-
-
Guimet, E.1
Parada, J.2
Ruiz, A.3
Claver, C.4
Diéguez, M.5
|