-
1
-
-
0003868337
-
-
Kluwer Academic Publishers, Dordrecht
-
a) Rhodium Catalyzed Hydroformylation, Vol. 22, (Eds.: P. W. N. M. Van Leeuwen, C. Claver), Kluwer Academic Publishers, Dordrecht, 2000;
-
(2000)
Rhodium Catalyzed Hydroformylation
, vol.22
-
-
Van Leeuwen, P.W.N.M.1
Claver, C.2
-
3
-
-
33746300381
-
-
c) B. Breit, Angew. Chem. 2005, 117, 6976-6986;
-
(2005)
Angew. Chem.
, vol.117
, pp. 6976-6986
-
-
Breit, B.1
-
4
-
-
27544471835
-
-
Angew. Chem. Int. Ed. 2005, 44, 6816-6825;
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6816-6825
-
-
-
5
-
-
84867957605
-
-
d) R. Franke, D. Selent, A. Börner, Chem. Rev. 2012, 112, 5675-5732.
-
(2012)
Chem. Rev.
, vol.112
, pp. 5675-5732
-
-
Franke, R.1
Selent, D.2
Börner, A.3
-
6
-
-
0000613575
-
-
a) F. Agbossou, J. F. Carpentier, A. Mortreaux, Chem. Rev. 1995, 95, 2485-2506;
-
(1995)
Chem. Rev.
, vol.95
, pp. 2485-2506
-
-
Agbossou, F.1
Carpentier, J.F.2
Mortreaux, A.3
-
7
-
-
0000158150
-
-
(Eds.: P. W. N. M. Van Leeuwen, C. Claver), Kluwer Academic Publishers, Dordrecht
-
b) C. Claver, P. W. N. M. Van Leeuwen, in: Rhodium Catalyzed Hydroformylation, Vol. 22, (Eds.: P. W. N. M. Van Leeuwen, C. Claver), Kluwer Academic Publishers, Dordrecht, 2000, pp 107-124;
-
(2000)
Rhodium Catalyzed Hydroformylation
, vol.22
, pp. 107-124
-
-
Claver, C.1
Van Leeuwen, P.W.N.M.2
-
8
-
-
3843136482
-
-
c) M. Diéguez, O. Pàmies, C. Claver, Tetrahedron: Asymmetry 2004, 15, 2113-2122;
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 2113-2122
-
-
Diéguez, M.1
Pàmies, O.2
Claver, C.3
-
9
-
-
33748998999
-
-
d) C. Claver, M. Diéguez, O. Pàmies, S. Castillón, Top. Organomet. Chem. 2006, 18, 35-64;
-
(2006)
Top. Organomet. Chem.
, vol.18
, pp. 35-64
-
-
Claver, C.1
Diéguez, M.2
Pàmies, O.3
Castillón, S.4
-
11
-
-
84890112160
-
-
f) S. H. Chikkali, J. I. van der Vlugt, J. N. H. Reek, Coord. Chem. Rev. 2014, 262, 1-15.
-
(2014)
Coord. Chem. Rev.
, vol.262
, pp. 1-15
-
-
Chikkali, S.H.1
Van Der Vlugt, J.I.2
Reek, J.N.H.3
-
12
-
-
0025938381
-
-
a) C. Botteghi, S. Paganelli, A. Schionato, M. Marchetti, Chirality 1991, 3, 355-369;
-
(1991)
Chirality
, vol.3
, pp. 355-369
-
-
Botteghi, C.1
Paganelli, S.2
Schionato, A.3
Marchetti, M.4
-
13
-
-
84879386908
-
-
b) S. Ho, C. Bucher, J. L. Leighton, Angew. Chem. Int. Ed. 2013, 52, 6757-6761;
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 6757-6761
-
-
Ho, S.1
Bucher, C.2
Leighton, J.L.3
-
17
-
-
85013461641
-
-
N. Sakai, S. Mano, K. Nozaki, H. Takaya, J. Am. Chem. Soc. 1993, 115, 7033-7034.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 7033-7034
-
-
Sakai, N.1
Mano, S.2
Nozaki, K.3
Takaya, H.4
-
19
-
-
75249103032
-
-
b) X. W. Zhang, B. N. Cao, Y. J. Yan, S. C. Yu, B. M. Ji, X. M. Zhang, Chem. Eur. J. 2010, 16, 871-877.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 871-877
-
-
Zhang, X.W.1
Cao, B.N.2
Yan, Y.J.3
Yu, S.C.4
Ji, B.M.5
Zhang, X.M.6
-
20
-
-
84892616755
-
-
G. M. Noonan, C. J. Cobley, T. Mahoney, M. L. Clarke, Chem. Commun. 2014, 50, 1475-1477.
-
(2014)
Chem. Commun.
, vol.50
, pp. 1475-1477
-
-
Noonan, G.M.1
Cobley, C.J.2
Mahoney, T.3
Clarke, M.L.4
-
21
-
-
0034618483
-
-
M. Dieguez, O. Pamies, A. Ruiz, S. Castillon, C. Claver, Chem. Commun. 2000, 1607-1608.
-
(2000)
Chem. Commun.
, pp. 1607-1608
-
-
Dieguez, M.1
Pamies, O.2
Ruiz, A.3
Castillon, S.4
Claver, C.5
-
22
-
-
17144407219
-
-
a) T. P. Clark, C. R. Landis, S. L. Freed, J. Klosin, K. A. Abboud, J. Am. Chem. Soc. 2005, 127, 5040-5042;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 5040-5042
-
-
Clark, T.P.1
Landis, C.R.2
Freed, S.L.3
Klosin, J.4
Abboud, K.A.5
-
23
-
-
61349139400
-
-
b) A. L. Watkins, B. G. Hashiguchi, C. R. Landis, Org. Lett. 2008, 10, 4553-4556.
-
(2008)
Org. Lett.
, vol.10
, pp. 4553-4556
-
-
Watkins, A.L.1
Hashiguchi, B.G.2
Landis, C.R.3
-
24
-
-
0001855867
-
-
D. Seebach, A. K. Beck, A. Heckel, Angew. Chem. 2001, 113, 96-142;
-
(2001)
Angew. Chem.
, vol.113
, pp. 96-142
-
-
Seebach, D.1
Beck, A.K.2
Heckel, A.3
-
26
-
-
53849147602
-
-
B. Zhao, X. Peng, Z. Wang, C. Xia, K. Ding, Chem. Eur. J. 2008, 14, 7847-7857.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 7847-7857
-
-
Zhao, B.1
Peng, X.2
Wang, Z.3
Xia, C.4
Ding, K.5
-
27
-
-
74549156252
-
-
a) T. Robert, Z. Abiri, J. Wassenaar, A. J. Sandee, S. Romanski, J. M. Neudörfl, H. G. Schmalz, J. N. H. Reek, Organometallics 2010, 29, 478-483;
-
(2010)
Organometallics
, vol.29
, pp. 478-483
-
-
Robert, T.1
Abiri, Z.2
Wassenaar, J.3
Sandee, A.J.4
Romanski, S.5
Neudörfl, J.M.6
Schmalz, H.G.7
Reek, J.N.H.8
-
28
-
-
77953736613
-
-
b) J. Wassenaar, B. de Bruin, J. N. H. Reek, Organometallics 2010, 29, 2767-2776.
-
(2010)
Organometallics
, vol.29
, pp. 2767-2776
-
-
Wassenaar, J.1
De Bruin, B.2
Reek, J.N.H.3
-
29
-
-
84920853440
-
-
note
-
4 are generated as side products. Due to the presence of this acid, the enantioselectivity is most likely to be degraded by acid-catalyzed racemization.
-
-
-
-
30
-
-
84920853439
-
-
note
-
Purifying the aldehyde via chromatography caused a deterioration of the optical purity (65% ee).
-
-
-
-
31
-
-
84920853438
-
-
note
-
D of the isolated acids indicated that virtually no racemization occurred during oxidation.
-
-
-
-
32
-
-
84920853437
-
-
note
-
Exclusively the (S)-enantiomer of Naproxen is actually approved as a drug. Employing the opposite enantiomer of ligand 11a will provide the correct configuration.
-
-
-
|