-
2
-
-
33845470711
-
-
U.-H. Dolling, P. Davis, E. J. J. Grabowski, J. Am. Chem. Soc. 1984, 106, 446.
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 446
-
-
Dolling, U.-H.1
Davis, P.2
Grabowski, E.J.J.3
-
3
-
-
0000637655
-
-
D. L. Hughes, U.-H. Dolling, K. M. Ryan, E. F. Schoenewaldt, E. J. J. Grabowski, J. Org. Chem. 1987, 52, 4745.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 4745
-
-
Hughes, D.L.1
Dolling, U.-H.2
Ryan, K.M.3
Schoenewaldt, E.F.4
Grabowski, E.J.J.5
-
4
-
-
49349138832
-
-
The first asymmetric application of a cinchona-alkaloid-based PTC was reported for the enantioselective oxidation of unsaturated ketones.
-
The first asymmetric application of a cinchona-alkaloid-based PTC was reported for the enantioselective oxidation of unsaturated ketones:, R. Helder, J. C. Hummelen, R. W. P. M. Laane, J. S. Wiering, H. Wynberg, Tetrahedron Lett. 1976, 17, 1831.
-
(1976)
Tetrahedron Lett.
, vol.17
, pp. 1831
-
-
Helder, R.1
Hummelen, J.C.2
Laane, R.W.P.M.3
Wiering, J.S.4
Wynberg, H.5
-
5
-
-
33845185214
-
-
M. J. O'Donnell, W. D. Bennett, S. Wu, J. Am. Chem. Soc. 1989, 111, 2353
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 2353
-
-
O'Donnell, M.J.1
Bennett, W.D.2
Wu, S.3
-
6
-
-
0000234063
-
-
E. J. Corey, F. Xu, M. C. Noe, J. Am. Chem. Soc. 1997, 119, 12414
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 12414
-
-
Corey, E.J.1
Xu, F.2
Noe, M.C.3
-
9
-
-
77952900635
-
-
K. M. Belyk, B. Xiang, P. G. Bulger, W. R. Leonard, J. Balsells, J. Yin, C.-Y. Chen, Org. Process Res. Dev. 2010, 14, 692.
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 692
-
-
Belyk, K.M.1
Xiang, B.2
Bulger, P.G.3
Leonard, W.R.4
Balsells, J.5
Yin, J.6
Chen, C.-Y.7
-
10
-
-
84861575915
-
-
I. M. Bell, C. A. Stump, S. N. Gallicchio, D. D. Staas, C. B. Zartman, E. L. Moore, N. Sain, M. Urban, J. G. Bruno, A. Calamari, A. L. Kemmerer, S. D. Mosser, C. Fandozzi, R. B. White, M. M. Zrada, H. G. Selnick, S. L. Graham, J. P. Vacca, S. A. Kane, C. A. Salvatore, Bioorg. Med. Chem. Lett. 2012, 22, 3941.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 3941
-
-
Bell, I.M.1
Stump, C.A.2
Gallicchio, S.N.3
Staas, D.D.4
Zartman, C.B.5
Moore, E.L.6
Sain, N.7
Urban, M.8
Bruno, J.G.9
Calamari, A.10
Kemmerer, A.L.11
Mosser, S.D.12
Fandozzi, C.13
White, R.B.14
Zrada, M.M.15
Selnick, H.G.16
Graham, S.L.17
Vacca, J.P.18
Kane, S.A.19
Salvatore, C.A.20
more..
-
22
-
-
0033554053
-
-
T. Ooi, M. Kameda, K. Maruoka, J. Am. Chem. Soc. 1999, 121, 6519
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 6519
-
-
Ooi, T.1
Kameda, M.2
Maruoka, K.3
-
23
-
-
0013369828
-
-
H.-g. Park, B.-S. Jeong, M.-S. Yoo, J.-H. Lee, M.-k. Park, Y.-J. Lee, M.-J. Kim, S.-s. Jew, Angew. Chem. 2002, 114, 3162
-
(2002)
Angew. Chem.
, vol.114
, pp. 3162
-
-
Park, H.-G.1
Jeong, B.-S.2
Yoo, M.-S.3
Lee, J.-H.4
Park, M.-K.5
Lee, Y.-J.6
Kim, M.-J.7
Jew, S.-S.8
-
25
-
-
84875965574
-
-
Recently, new calculated transition state modeling of the PTC including the leaving group effect was reported.
-
Recently, new calculated transition state modeling of the PTC including the leaving group effect was reported:, E. deFreitas, J. R. Pliego, Jr., ACS Catal. 2013, 3, 613.
-
(2013)
ACS Catal.
, vol.3
, pp. 613
-
-
Defreitas, E.1
Pliego Jr., J.R.2
-
26
-
-
0001028942
-
-
Owing to the pseudoenantiomeric nature of cinchonidine with respect to cinchonine, the absolute configuration of product 11 was opposite to that of the product obtained with 9g
-
Owing to the pseudoenantiomeric nature of cinchonidine with respect to cinchonine, the absolute configuration of product 11 was opposite to that of the product obtained with 9g;, A. Bhattacharya, U.-H. Dolling, E. J. J. Grabowski, S. Karady, K. M. Ryan, L. M. Weinstock, Angew. Chem. 1986, 98, 442
-
(1986)
Angew. Chem.
, vol.98
, pp. 442
-
-
Bhattacharya, A.1
Dolling, U.-H.2
Grabowski, E.J.J.3
Karady, S.4
Ryan, K.M.5
Weinstock, L.M.6
|