-
4
-
-
0030860279
-
-
M. Tokunaga, J. F. Larrow, F. Kakiuchi, E. N. Jacobsen, Science 1997, 277, 936-938.
-
(1997)
Science
, vol.277
, pp. 936-938
-
-
Tokunaga, M.1
Larrow, J.F.2
Kakiuchi, F.3
Jacobsen, E.N.4
-
6
-
-
0034697497
-
-
in, Wiley-VCH, Weinheim
-
H. U. Blaser, E. Schmidt in Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions, Wiley-VCH, Weinheim, 2004, pp.165-199.
-
(2004)
Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions
, pp. 165-199
-
-
Blaser, H.U.1
Schmidt, E.2
-
9
-
-
0037091011
-
-
J. M. Ready, E. N. Jacobsen, Angew. Chem. 2002, 114, 1432-1435; Angew. Chem. Int. Ed. 2002, 41, 1374-1377.
-
(2002)
Angew. Chem. 2002, 114, 1432-1435; Angew. Chem. Int. Ed.
, vol.41
, pp. 1374-1377
-
-
Ready, J.M.1
Jacobsen, E.N.2
-
10
-
-
0034675617
-
-
R. Breinbauer, E. N. Jacobsen, Angew. Chem. 2000, 112, 3750-3753; Angew. Chem. Int. Ed. 2000, 39, 3604-3607.
-
(2000)
Angew. Chem. 2000, 112, 3750-3753; Angew. Chem. Int. Ed.
, vol.39
, pp. 3604-3607
-
-
Breinbauer, R.1
Jacobsen, E.N.2
-
12
-
-
33846783022
-
-
X. Zheng, C. W. Jones, M. Weck, J. Am. Chem. Soc. 2007, 129, 1105-1112.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 1105-1112
-
-
Zheng, X.1
Jones, C.W.2
Weck, M.3
-
14
-
-
38849126242
-
-
X. Zheng, C. W. Jones, M. Weck, Adv. Synth. Catal. 2008, 350, 255-261.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 255-261
-
-
Zheng, X.1
Jones, C.W.2
Weck, M.3
-
15
-
-
33746214596
-
-
B. M. Rossbach, K. Leopold, R. Weberskirch, Angew. Chem. 2006, 118, 1331-1335; Angew. Chem. Int. Ed. 2006, 45, 1309-1312.
-
(2006)
Angew. Chem. 2006, 118, 1331-1335; Angew. Chem. Int. Ed.
, vol.45
, pp. 1309-1312
-
-
Rossbach, B.M.1
Leopold, K.2
Weberskirch, R.3
-
18
-
-
77954769635
-
-
A. Zulauf, M. Mellah, X. Hong, E. Schulz, Dalton Trans. 2010, 39, 6911-6935.
-
(2010)
Dalton Trans.
, vol.39
, pp. 6911-6935
-
-
Zulauf, A.1
Mellah, M.2
Hong, X.3
Schulz, E.4
-
19
-
-
34548798131
-
-
H. Yang, L. Zhang, L. Zhong, Q. Yang, C. Li, Angew. Chem. 2007, 119, 6985-6989; Angew. Chem. Int. Ed. 2007, 46, 6861-6865.
-
(2007)
Angew. Chem. 2007, 119, 6985-6989; Angew. Chem. Int. Ed.
, vol.46
, pp. 6861-6865
-
-
Yang, H.1
Zhang, L.2
Zhong, L.3
Yang, Q.4
Li, C.5
-
22
-
-
29544446558
-
-
X. Zheng, C. W. Jones, M. Weck, Chem. Eur. J. 2006, 12, 576-583.
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 576-583
-
-
Zheng, X.1
Jones, C.W.2
Weck, M.3
-
23
-
-
33947528653
-
-
W. Solodenko, G. Jas, U. Kunz, A. Kirschning, Synthesis 2007, 4, 583-589.
-
(2007)
Synthesis
, vol.4
, pp. 583-589
-
-
Solodenko, W.1
Jas, G.2
Kunz, U.3
Kirschning, A.4
-
24
-
-
53749085864
-
-
A. Zulauf, M. Mellah, R. Guillot, E. Schulz, Eur. J. Org. Chem. 2008, 2118-2129.
-
(2008)
Eur. J. Org. Chem.
, pp. 2118-2129
-
-
Zulauf, A.1
Mellah, M.2
Guillot, R.3
Schulz, E.4
-
25
-
-
64249145892
-
-
A. Zulauf, M. Mellah, E. Schulz, J. Org. Chem. 2009, 74, 2242-2245.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2242-2245
-
-
Zulauf, A.1
Mellah, M.2
Schulz, E.3
-
27
-
-
33344471527
-
-
See also reference[24].
-
A. Voituriez, M. Mellah, E. Schulz, Synth. Met. 2006, 156, 166-175. See also reference[24].
-
(2006)
Synth. Met.
, vol.156
, pp. 166-175
-
-
Voituriez, A.1
Mellah, M.2
Schulz, E.3
-
28
-
-
0037138704
-
-
S. E. Schaus, B. D. Brandes, J. F. Larrow, M. Tokunaga, K. B. Hansen, A. E. Gould, M. E. Furrow, E. N. Jacobsen, J. Am. Chem. Soc. 2002, 124, 1307-1315.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1307-1315
-
-
Schaus, S.E.1
Brandes, B.D.2
Larrow, J.F.3
Tokunaga, M.4
Hansen, K.B.5
Gould, A.E.6
Furrow, M.E.7
Jacobsen, E.N.8
-
29
-
-
35848948222
-
-
W.-H. Leung, E. Y. Y. Chan, E. K. F. Chow, I. D. Williams, S.-M. Peng, J. Chem. Soc. Dalton Trans. 1996, 1229-1236.
-
(1996)
J. Chem. Soc. Dalton Trans.
, pp. 1229-1236
-
-
Leung, W.-H.1
Chan, E.Y.Y.2
Chow, E.K.F.3
Williams, I.D.4
Peng, S.-M.5
-
30
-
-
84864374081
-
-
For experimental details, see the Supporting Information.
-
For experimental details, see the Supporting Information.
-
-
-
-
31
-
-
0000180260
-
-
M. E. Furrow, S. E. Schaus, E. N. Jacobsen, J. Org. Chem. 1998, 63, 6776-6777.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6776-6777
-
-
Furrow, M.E.1
Schaus, S.E.2
Jacobsen, E.N.3
-
32
-
-
1042265088
-
-
L. P. C. Nielsen, C. P. Stevenson, D. G. Blackmond, E. N. Jacobsen, J. Am. Chem. Soc. 2004, 126, 1360-1362.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 1360-1362
-
-
Nielsen, L.P.C.1
Stevenson, C.P.2
Blackmond, D.G.3
Jacobsen, E.N.4
-
33
-
-
84864374083
-
-
In reference[9], the existence of a monometallic mechanism was also suggested in some HKR transformations under specific conditions (for instance, with oligomeric catalysts in dilute conditions).
-
In reference[9], the existence of a monometallic mechanism was also suggested in some HKR transformations under specific conditions (for instance, with oligomeric catalysts in dilute conditions).
-
-
-
-
34
-
-
35648948878
-
-
S. Jain, X. Zheng, C. W. Jones, M. Weck, R. J. Davis, Inorg. Chem. 2007, 46, 8887-8896.
-
(2007)
Inorg. Chem.
, vol.46
, pp. 8887-8896
-
-
Jain, S.1
Zheng, X.2
Jones, C.W.3
Weck, M.4
Davis, R.J.5
-
35
-
-
84864372738
-
-
III-OH sites during the polymerization.
-
III-OH sites during the polymerization.
-
-
-
-
36
-
-
71249139742
-
-
S. Jain, K. Venkatasubbaiah, C. W. Jones, R. J. Davis, J. Mol. Catal. A 2010, 316, 8-15.
-
(2010)
J. Mol. Catal. A
, vol.316
, pp. 8-15
-
-
Jain, S.1
Venkatasubbaiah, K.2
Jones, C.W.3
Davis, R.J.4
-
37
-
-
53849141862
-
-
C. S. Gill, K. Venkatasubbaiah, N. T. S. Phan, M. Weck, C. W. Jones, Chem. Eur. J. 2008, 14, 7306-7313.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 7306-7313
-
-
Gill, C.S.1
Venkatasubbaiah, K.2
Phan, N.T.S.3
Weck, M.4
Jones, C.W.5
-
39
-
-
84864342211
-
-
Note
-
A control experiment was performed to check if catalyst-leaching occurred during the recycling procedure. After 5h in the dynamic HKR of epibromohydrin, an aliquot was removed to check the conversion (30%). The mixture was diluted with THF and stirred for an additional 12h to reach 42% conversion (and 80%ee). The polymer was then removed by filtration and the recovered filtrate was stirred for a further 24h. No further modification in the composition of the solution was detected, thus confirming that the catalyst had been entirely suppressed.
-
-
-
-
40
-
-
84864374080
-
-
Note
-
The cobalt content of polymer 5 before and after 11cycles were 6.04% and 6.26%, respectively, as determined by elemental analysis. The slight increase in cobalt content might have originated from the hydrolysis of the Co-OAc units during the reaction or elimination of impurities from the original polymer.
-
-
-
-
41
-
-
84864342213
-
-
Note
-
The Co/F ratio was determined by elemental analysis in the fresh polymer and after reuse (after the 11th and 12thcycles) to be 1:0.64, 1:0.67, and 1:0.60.
-
-
-
|