-
1
-
-
45249098601
-
Chiral Drugs. An Overview
-
Lien Ai Nguyen, Hua He, Chuong Pham-Huy, Chiral Drugs. An Overview, International Journal of Biomedical Science 2(2), (2006) 85-100
-
(2006)
International Journal of Biomedical Science
, vol.2
, Issue.2
, pp. 85-100
-
-
Nguyen, L.A.1
He, H.2
Pham-Huy, C.3
-
3
-
-
0026457938
-
Improved chiral recognition of some compounds via the simultaneous use of beta-cyclodextrin and its permethylated derivative in a reversedphase high-performance liquid chromatographic system
-
D. Sybilska, A. Bielejewska, R. Nowakowski, K. Duszczyk and J. Jurczak, Improved chiral recognition of some compounds via the simultaneous use of beta-cyclodextrin and its permethylated derivative in a reversedphase high-performance liquid chromatographic system, J. Chromatogr., 625,349-352 (1992).
-
(1992)
J. Chromatogr.
, vol.625
, pp. 349-352
-
-
Sybilska, D.1
Bielejewska, A.2
Nowakowski, R.3
Duszczyk, K.4
Jurczak, J.5
-
4
-
-
0027165511
-
Chiral stationary phases in concert with homologous chiral mobile phase additives: Pusldpull model
-
K.J. Duff, H.L. Gray, R.J. Gray and C.C. Bahler, Chiral stationary phases in concert with homologous chiral mobile phase additives: Pusldpull model, Chirality, 5,201-206 (1993).
-
(1993)
Chirality
, vol.5
, pp. 201-206
-
-
Duff, K.J.1
Gray, H.L.2
Gray, R.J.3
Bahler, C.C.4
-
5
-
-
0000610839
-
Enantioselectivity of complex formation in ligandexchange chromatographic systems with chiral stationary and or chiral mobile phases
-
V.A. Davankov, A.A. Kurganov and T.M. Ponomareva, Enantioselectivity of complex formation in ligandexchange chromatographic systems with chiral stationary and or chiral mobile phases, J. Chromatogr., 452,
-
J. Chromatogr.
, vol.452
-
-
Davankov, V.A.1
Kurganov, A.A.2
Ponomareva, T.M.3
-
6
-
-
0025685319
-
A vivid model illustrating chiral recognition induced by achiral structures
-
V.A. Davankov, V.R. Meyer and M. Rais, A vivid model illustrating chiral recognition induced by achiral structures, Chirality, 2,208-210 (1990).
-
(1990)
Chirality
, vol.2
, pp. 208-210
-
-
Davankov, V.A.1
Meyer, V.R.2
Rais, M.3
-
7
-
-
77953405020
-
-
A.M. Krstulovic, Editor, Ellis Horwood
-
A.M. Krstulovic, Editor, Chiral Separations by HPLC, Applications to Pharmaceutical Compounds, Ellis Horwood, 1989,548 pp.
-
(1989)
Chiral Separations by HPLC, Applications to Pharmaceutical Compounds
, pp. 548
-
-
-
8
-
-
0020895171
-
Resolution of racemates by high-performance liquid chromatography, a h
-
V.A. Davankov, A.A. Kurganov and AS. Bochkov, Resolution of racemates by high-performance liquid chromatography, A h . Chromatogr., 22,71-116 (1983).
-
(1983)
Chromatogr.
, vol.22
, pp. 71-116
-
-
Davankov, V.A.1
Kurganov, A.A.2
Bochkov, A.S.3
-
11
-
-
11744286228
-
Consideration of chiral recognition relevant to the liquid chromatographic separation of enantiomers
-
W.H. Pirkle and T.C. Pochapsky, Consideration of chiral recognition relevant to the liquid chromatographic separation of enantiomers, Chem. Rev., 89,347-362 (1989).
-
(1989)
Chem. Rev.
, vol.89
, pp. 347-362
-
-
Pirkle, W.H.1
Pochapsky, T.C.2
-
12
-
-
77953369456
-
-
(ACS Symposium Series, No. 471), ed. by S. Ahuja, American Chemical Society, Washington, DC
-
Chiral Separations by Liquid Chromatography (ACS Symposium Series, No. 471), ed. by S. Ahuja, American Chemical Society, Washington, DC, 1991,239 pp.
-
(1991)
Chiral Separations by Liquid Chromatography
, pp. 239
-
-
-
17
-
-
77953365018
-
Basic Terminology of Stereochemistry (IUPAC Recommendations 1996)
-
2193-2222
-
G.P.Moss, Basic Terminology of Stereochemistry (IUPAC Recommendations 1996), Pure Appl. Chem., 68, J. Chromatogr. A, 666,565-601 (1994). 2193-2222 (1996).
-
(1994)
Pure Appl. Chem., 68, J. Chromatogr. a
, vol.666
, pp. 565-601
-
-
Moss, G.P.1
-
18
-
-
0035847205
-
Enantioselective chromatography as a powerful alternative for the preparation of drug enantiomers
-
DOI 10.1016/S0021-9673(00)00951-1, PII S0021967300009511
-
Francotte, E.R., "Enantioselective chromatography as a powerful alternative for the preparation of drug enantiomers", J. Chromatogr., 2001, 906, 379-397. (Pubitemid 32056212)
-
(2001)
Journal of Chromatography a
, vol.906
, Issue.1-2
, pp. 379-397
-
-
Francotte, E.R.1
-
19
-
-
0037207268
-
Preparative chiral chromatographic resolution of enantiomers in drug discovery
-
DOI 10.1016/S0165-022X(02)00126-4, PII S0165022X02001264
-
Andersson, S. and Allenmark, S.G., "Preparative chiral chromatographic resolution of enantiomers in drug discovery", J. Biochem. Biophys. Methods, 2002, 54, 11-23. (Pubitemid 36126133)
-
(2002)
Journal of Biochemical and Biophysical Methods
, vol.54
, Issue.1-3
, pp. 11-23
-
-
Andersson, S.1
Allenmark, S.G.2
-
20
-
-
0035458159
-
Industrial chiral chromatography: The keys to rapid process development and successful implementation. Part 1
-
Blehaut, J., Ludemann-Hombourger, O. and Perrin, S.R., "Industrial chiral chromatography: the keys to rapid process development and successful implementation", Chim. Oggi, 2001, (Sept.), 24-28. (Pubitemid 33402384)
-
(2001)
Chimica Oggi
, vol.19
, Issue.9
, pp. 24-28
-
-
Blehaut, J.1
Ludemann-Hombourger, O.2
Perrin, S.R.3
-
21
-
-
0035847187
-
Preparative enantioseparation by simulated moving bed chromatography
-
DOI 10.1016/S0021-9673(00)00956-0, PII S0021967300009560
-
Schulte, M. and Strube, J., "Preparative enantioseparation by simulated moving bed chromatography", J.Chromatogr. A, 2001, 906, 399-416. (Pubitemid 32056213)
-
(2001)
Journal of Chromatography a
, vol.906
, Issue.1-2
, pp. 399-416
-
-
Schulte, M.1
Strube, J.2
-
22
-
-
0036260488
-
Impact of a modification in the production process of an amylose derived stationary phase on the SMB separation of a pharmaceutical intermediate
-
DOI 10.1081/SS-120002737
-
Huthmann, E. and Juza, M., "Impact of a modification in the production process of an amylose derived stationary phase on the SMB separation of a pharmaceutical intermediate", Sep. Sci. Technol., 2002, 37, 1567-1590. (Pubitemid 34587289)
-
(2002)
Separation Science and Technology
, vol.37
, Issue.7
, pp. 1567-1590
-
-
Huthmann, E.1
Juza, M.2
-
23
-
-
1842506638
-
Chromatography as an enabling technology in pharmaceutical process development: Expedited multikilogram preparation of a candidate HIV protease inhibitor
-
DOI 10.1021/op0300443
-
Welch, C.J., Fleitz, F., Antia, F., Yehl, P.,Waters, R., Ikemoto, N., Armstrong, J.D. and Mathre, D.J., "Chromatography as an enabling technology in pharmaceutical process development: expedited multikilogram preparation of a candidate HIV protease inhibitor", Org. Proc. Res. Dev., 2004, 8(2), 186-191. (Pubitemid 38453164)
-
(2004)
Organic Process Research and Development
, vol.8
, Issue.2
, pp. 186-191
-
-
Welch, C.J.1
Fleitz, F.2
Antia, F.3
Yehl, P.4
Waters, R.5
Ikemoto, N.6
Armstrong III, J.D.7
Mathre, D.J.8
-
24
-
-
1642443189
-
Reactive resin facilitated preparation of an enantiopure fluorobicycloketone
-
Wong, A., Welch, C.J., Kuethe, J.T., Vazquez, E., Shaimi, M., Henderson , D., Davies, I.W. and Hughes, D.L., "Reactive resin facilitated preparation of an enantiopure fluorobicycloketone", Org. Biomol. Chem., 2004, 2(2), 168-174.
-
(2004)
Org. Biomol. Chem.
, vol.2
, Issue.2
, pp. 168-174
-
-
Wong, A.1
Welch, C.J.2
Kuethe, J.T.3
Vazquez, E.4
Shaimi, M.5
Henderson, D.6
Davies, I.W.7
Hughes, D.L.8
-
25
-
-
7044271785
-
Chiral chromatography: Given the new techniques currently in development, the use of chiral chromatography in the large-scale separation of racemic compounds will eventually become commonplace
-
Cox, G.B., "Chiral chromatography: given the new techniques currently in development, the use of chiral chromatography in the large-scale separation of racemic compounds will eventually become commonplace", Innovat. Pharm. Technol., 2001, 1, 131-137.
-
(2001)
Innovat. Pharm. Technol.
, vol.1
, pp. 131-137
-
-
Cox, G.B.1
-
26
-
-
0003942864
-
-
John Wiley & Sons, New York
-
Eliel, E.L., Wilen, S.H. and Maunder, L.N., Stereochemistry of Organic Compounds, John Wiley & Sons, New York , 1994.
-
(1994)
Stereochemistry of Organic Compounds
-
-
Eliel, E.L.1
Wilen, S.H.2
Maunder, L.N.3
-
27
-
-
11844251094
-
Chiral Chemistry Special Issue
-
May 5
-
Chiral Chemistry Special Issue, Chem. Eng. News, May 5, 2003 , 81 (18).
-
(2003)
Chem. Eng. News
, vol.81
, Issue.18
-
-
-
28
-
-
0034529375
-
Asymmetric processes in the large-scale preparation of chiral drug candidates
-
O'Brien, M.K. and Vanasse, B., "Asymmetric processes in the large-scale preparation of chiral drug candidates", Curr. Opin. Drug Dis. Dev., 2000, 3(6), 793-806. (Pubitemid 32007065)
-
(2000)
Current Opinion in Drug Discovery and Development
, vol.3
, Issue.6
, pp. 793-806
-
-
O'Brien, M.K.1
Vanasse, B.2
-
29
-
-
0030249955
-
Chirotechnology: Designing economic chiral synthesis
-
Sheldon, R.A., "Chirotechnology: designing economic chiral synthesis", J. Chem. Technol. Biotechnol., 1996, 67(1), 1-14.
-
(1996)
J. Chem. Technol. Biotechnol.
, vol.67
, Issue.1
, pp. 1-14
-
-
Sheldon, R.A.1
-
31
-
-
0000305326
-
Beyond nature's chiral pool: Enantioselective catalysis in industry
-
Nugent, W.A., RajanBabu, T.V. and Burk, M.J., "Beyond nature's chiral pool: enantioselective catalysis in industry", Science, 1993, 259 (5094), 479-483.
-
(1993)
Science
, vol.259
, Issue.5094
, pp. 479-483
-
-
Nugent, W.A.1
Rajanbabu, T.V.2
Burk, M.J.3
-
32
-
-
0002165370
-
Studies in asymmetric synthesis. the development of practical chiral enolate synthons
-
Evans, D.A., "Studies in asymmetric synthesis. The development of practical chiral enolate synthons", Aldrichim. Acta, 1982, 15(2), 23-32.
-
(1982)
Aldrichim. Acta
, vol.15
, Issue.2
, pp. 23-32
-
-
Evans, D.A.1
-
33
-
-
0038122853
-
Recent advances in asymmetric synthesis with chiral imide auxiliaries
-
Evans, D.A. and Shaw, J.T., "Recent advances in asymmetric synthesis with chiral imide auxiliaries", Actual. Chim., 2003, (4-5), 35-38. (Pubitemid 36765136)
-
(2003)
Actualite Chimique
, Issue.4-5
, pp. 35-38
-
-
Evans, D.A.1
Shaw, J.T.2
-
34
-
-
0001428655
-
Chiral oxazolines - Their legacy as key players in the renaissance of asymmetric synthesis
-
Meyers, A.I., "Chiral oxazolines - their legacy as key players in the renaissance of asymmetric synthesis", J. Heterocycl. Chem., 1998, 35 (5), 991-1002.
-
(1998)
J. Heterocycl. Chem.
, vol.35
, Issue.5
, pp. 991-1002
-
-
Meyers, A.I.1
-
35
-
-
0031047517
-
Chiral bicyclic lactams: Useful precursors and templates for asymmetric syntheses
-
Meyers, A.I. and Brengel, G.P., "Chiral bicyclic lactams: useful precursors and templates for asymmetric syntheses", Chem. Commun., 1997, (1), 1-8. (Pubitemid 27062878)
-
(1997)
Chemical Communications
, Issue.1
, pp. 1-8
-
-
Meyers, A.I.1
Brengel, G.P.2
-
36
-
-
37649026114
-
TADDOLS, their derivatives, and TADDOL analogues: Versatile chiral auxiliaries
-
Seebach, D., Beck, A.K. and Heckel, A., "TADDOLs, their derivatives, and TADDOL analogs: versatile chiral auxiliaries", Angew. Chem., Int. Ed., 2001, 40(1), 92-138. (Pubitemid 33593274)
-
(2001)
Angewandte Chemie (International Edition in English)
, vol.40
, Issue.1
-
-
Seebach, D.1
Beck, A.K.2
Heckel, A.3
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