-
1
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-
34250658477
-
-
The new FDA guidelines on chiral drugs: Chirality 1992, 4, 338-340.
-
The new FDA guidelines on chiral drugs: Chirality 1992, 4, 338-340.
-
-
-
-
2
-
-
0004127585
-
-
Reviews on combinatorial chemistry: a) K. C. Nicolaou, R. Hanko, W. Hartwig Eds, Wiley-VCH, Weinheim
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Reviews on combinatorial chemistry: a) K. C. Nicolaou, R. Hanko, W. Hartwig (Eds.), Handbook of Combinatorial Chemistry: Drugs, Catalysts, Materials, Wiley-VCH, Weinheim, 2002;
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(2002)
Handbook of Combinatorial Chemistry: Drugs, Catalysts, Materials
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3
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0001625156
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Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin, ch. 39;
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b) K. D. Shimizu, M. L. Snapper, A. H. Hoveyda in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999, vol. 3, ch. 39;
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(1999)
Comprehensive Asymmetric Catalysis
, vol.3
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Shimizu, K.D.1
Snapper, M.L.2
Hoveyda, A.H.3
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5
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0003501419
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S. Miertus, G. Fassina Eds, Marcel Dekker, New York
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d) S. Miertus, G. Fassina (Eds.), Combinatorial Chemistry and Technology, Marcel Dekker, New York, 1997;
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(1997)
Combinatorial Chemistry and Technology
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7
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0000486957
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f) M. T. Reetz, Angew. Chem. 2001, 113, 292-320;
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(2001)
Angew. Chem
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, pp. 292-320
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Reetz, M.T.1
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8
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0035910597
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Angew. Chem. Int. Ed. 2001, 40, 284-310;
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(2001)
Chem. Int. Ed
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, pp. 284-310
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Angew1
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0001064205
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g) T. Bein, Angew. Chem. 1999, 111, 335-338;
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(1999)
Angew. Chem
, vol.111
, pp. 335-338
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Bein, T.1
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10
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0033082641
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Angew. Chem. Int. Ed. 1999, 38, 323-326.
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(1999)
Chem. Int. Ed
, vol.38
, pp. 323-326
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-
Angew1
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11
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18844444146
-
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Reviews on high-throughput screening: a) A. Hagemeyer, P. Strasser, A. F. Volpe Jr Eds, Wiley-VCH, Weinheim
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Reviews on high-throughput screening: a) A. Hagemeyer, P. Strasser, A. F. Volpe Jr (Eds.), High-Throughput Screening in Chemical Catalysis, Wiley-VCH, Weinheim, 2004;
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(2004)
High-Throughput Screening in Chemical Catalysis
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12
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0003485353
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J. P. Devlin Ed, Marcel Dekker, New York
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b) J. P. Devlin (Ed.), High-Throughput Screening, Marcel Dekker, New York, 1997;
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(1997)
High-Throughput Screening
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13
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0000425928
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c) M. T. Reetz, Angew. Chem. 2002, 114, 1391-1394;
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(2002)
Angew. Chem
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, pp. 1391-1394
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Reetz, M.T.1
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14
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0037090667
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Angew. Chem. Int. Ed 2002, 41, 1335-1338;
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(2002)
Chem. Int. Ed
, vol.41
, pp. 1335-1338
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Angew1
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0000462177
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d) B. Jandeleit, D. J. Schaefer, T. S. Powers, H. W. Turner, W. H. Weinberg, Angew. Chem. 1999, 111, 2648-2689;
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Angew. Chem
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, pp. 2648-2689
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Jandeleit, B.1
Schaefer, D.J.2
Powers, T.S.3
Turner, H.W.4
Weinberg, W.H.5
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16
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0033520302
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Angew. Chem. Int. Ed. 1999, 38, 2494-2532;
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(1999)
Chem. Int. Ed
, vol.38
, pp. 2494-2532
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0031732777
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g) K. D. Shimizu, M. L. Snapper, A. H. Hoveyda, Chem. Eur. J. 1998, 4, 1885-1889.
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Chem. Eur. J
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, pp. 1885-1889
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Shimizu, K.D.1
Snapper, M.L.2
Hoveyda, A.H.3
-
20
-
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34250688737
-
-
Excellent examples of combinatorial library and high-throughput screening thereof: a B. M. Cole, K. D. Shimizu, C. A. Krueger, J. P. A. Harrity, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1996, 108, 1776-1779;
-
Excellent examples of combinatorial library and high-throughput screening thereof: a) B. M. Cole, K. D. Shimizu, C. A. Krueger, J. P. A. Harrity, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1996, 108, 1776-1779;
-
-
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21
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0029764025
-
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Angew. Chem. Int. Ed. 1996, 35, 1668-1671;
-
(1996)
Chem. Int. Ed
, vol.35
, pp. 1668-1671
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-
Angew1
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24
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0033118620
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Angew. Chem. Int. Ed. 1999, 38, 937-941;
-
(1999)
Chem. Int. Ed
, vol.38
, pp. 937-941
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Angew1
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25
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0000545849
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d) M. T. Reetz, Angew. Chem. 2000, 112, 4049-4052;
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(2000)
Angew. Chem
, vol.112
, pp. 4049-4052
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Reetz, M.T.1
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26
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0034602059
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Angew. Chem. Int. Ed. 2000, 39, 3891-3893;
-
(2000)
Chem. Int. Ed
, vol.39
, pp. 3891-3893
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Angew1
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28
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4644233894
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Angew. Chem. Int. Ed. 2004, 43, 2498-2500;
-
(2004)
Chem. Int. Ed
, vol.43
, pp. 2498-2500
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Angew1
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29
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3142683773
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[9a-9e]
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[9a-9e]
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31
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0042848836
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-
In collaboration with Takeuchi, we reported the asymmetric reduction of fluorous ketones but not fluorous cleavable tagged, as the antecedent of prochiral substrates. Y. Nakamura, S. Takeuchi, K. Okumura, Y. Ohgo, H. Matsuzawa, K. Mikami, Tetrahedron Lett. 2003, 44, 6221-6225;
-
b) In collaboration with Takeuchi, we reported the asymmetric reduction of fluorous ketones but not fluorous cleavable tagged, as the antecedent of prochiral substrates. Y. Nakamura, S. Takeuchi, K. Okumura, Y. Ohgo, H. Matsuzawa, K. Mikami, Tetrahedron Lett. 2003, 44, 6221-6225;
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-
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33
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3943071029
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d) D. P. Curran, S. Dandapani, S. Werner, M. Matsugi, Synlett 2004, 1545-1548;
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(2004)
Synlett
, pp. 1545-1548
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Curran, D.P.1
Dandapani, S.2
Werner, S.3
Matsugi, M.4
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34
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10844233858
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e) K. Mikami, H. Matsuzawa, S. Takeuchi, U. Nakamura, D. P. Curran, Synlett 2004, 2713-2716.
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(2004)
Synlett
, pp. 2713-2716
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-
Mikami, K.1
Matsuzawa, H.2
Takeuchi, S.3
Nakamura, U.4
Curran, D.P.5
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35
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34250656589
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Reviews: a D. P. Curran in The Handbook of Fluorous Chemistry (Eds.: J. A. Gladysz, D. P. Curran, I. T. Horvath). Wiley-VCH, Weinheim, 2004, ch. 8, He has classified FMS into three categories: 1) coding of enantiomers (quasiracemic synthesis), 2) coding of diastereomers, and 3) coding of analogues;
-
Reviews: a) D. P. Curran in The Handbook of Fluorous Chemistry (Eds.: J. A. Gladysz, D. P. Curran, I. T. Horvath). Wiley-VCH, Weinheim, 2004, ch. 8, He has classified FMS into three categories: 1) coding of enantiomers (quasiracemic synthesis), 2) coding of diastereomers, and 3) coding of analogues;
-
-
-
-
38
-
-
0035793878
-
-
Excellent examples of quasiracemic synthesis: d Z. Luo, Q. Zhang, Y. Oderaotoshi, D. P. Curran, Sci.. 2001, 291, 1766-1769;
-
Excellent examples of quasiracemic synthesis: d) Z. Luo, Q. Zhang, Y. Oderaotoshi, D. P. Curran, Sci.. 2001, 291, 1766-1769;
-
-
-
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39
-
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0037157184
-
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e) Q. Zhang, A. Rivikin, D. P. Curran, J. Am. Chem. Soc. 2002, 124, 5774-5781;
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(2002)
J. Am. Chem. Soc
, vol.124
, pp. 5774-5781
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Zhang, Q.1
Rivikin, A.2
Curran, D.P.3
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41
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34250322190
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g) D. P. Curran, G. Moura-Letts, M. Pohlman, Angew. Chem. 2006, 118, 2483-2486;
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(2006)
Angew. Chem
, vol.118
, pp. 2483-2486
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Curran, D.P.1
Moura-Letts, G.2
Pohlman, M.3
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42
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33746298355
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Angew. Chem. Int. Ed 2006, 45, 2423-2426;
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(2006)
Chem. Int. Ed
, vol.45
, pp. 2423-2426
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Angew1
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43
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33746291216
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h) C. S. Wilcox, V. Gundipati, H. Lu, S. Turkyilmaz, D. P. Curran, Angew. Chem. 2005, 117, 7098-7100;
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(2005)
Angew. Chem
, vol.117
, pp. 7098-7100
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Wilcox, C.S.1
Gundipati, V.2
Lu, H.3
Turkyilmaz, S.4
Curran, D.P.5
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44
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27544434009
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Angew. Chem. Int. Ed. 2005, 44, 6938-6940.
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(2005)
Chem. Int. Ed
, vol.44
, pp. 6938-6940
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Angew1
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45
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11744286228
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Reviews on a chiral stationary phase for HPLC: a W. H. Pirkle, T. C. Pochapsky, Chem. Rev. 1989, 89, 347-362;
-
Reviews on a chiral stationary phase for HPLC: a) W. H. Pirkle, T. C. Pochapsky, Chem. Rev. 1989, 89, 347-362;
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47
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0032482102
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Angew. Chem. Int. Ed. 1998, 37, 1020-1043.
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(1998)
Chem. Int. Ed
, vol.37
, pp. 1020-1043
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Angew1
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48
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0029949417
-
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See also the recent examples of a chiral stationary phase for HPLC; c E. Yashima, C. Yamamoto, Y. Okamoto, J. Am. Chem. Soc. 1996, 118, 4036-4048;
-
See also the recent examples of a chiral stationary phase for HPLC; c) E. Yashima, C. Yamamoto, Y. Okamoto, J. Am. Chem. Soc. 1996, 118, 4036-4048;
-
-
-
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50
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4544275995
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e) T. Kubota, C. Yamamoto, Y. Okamoto, J. Polym. Sci. Part A: Polym. Chem. 2004, 42, 4704-4710.
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J. Polym. Sci. Part A: Polym. Chem
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, pp. 4704-4710
-
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Kubota, T.1
Yamamoto, C.2
Okamoto, Y.3
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51
-
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34250639900
-
-
SUMICHIRAL OA-7000 series are sold by Sumika Chemical Analysis Service. Catalogue of SUMICHIRAL OA-7000 series: http://www.scas.co.jp/.SUMICHIRAL OA-7000 is the column with unmodified β-CD bonded to the silica gel by a saccharide (glucuroylgluconoyl group) spacer; SUMICHIRAL OA-7100 is the column with unmodified P-CD bonded to the silica gel by an alkyl group spacer; SUMICHIRAL OA-7500 is the column with P-CD, in which the hydroxy group is protected by a methyl group and bonded to the silica gel by an alkyl group spacer.
-
SUMICHIRAL OA-7000 series are sold by Sumika Chemical Analysis Service. Catalogue of SUMICHIRAL OA-7000 series: http://www.scas.co.jp/.SUMICHIRAL OA-7000 is the column with unmodified β-CD bonded to the silica gel by a saccharide (glucuroylgluconoyl group) spacer; SUMICHIRAL OA-7100 is the column with unmodified P-CD bonded to the silica gel by an alkyl group spacer; SUMICHIRAL OA-7500 is the column with P-CD, in which the hydroxy group is protected by a methyl group and bonded to the silica gel by an alkyl group spacer.
-
-
-
-
52
-
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0035793270
-
-
Circular dichroism/ultraviolet (CD/UV) or optical rotation/refractive index unit (OR/RIU) HPLC spectroscopy to determine the enantiomeric excesses of products: a) K. Mikami, R. Angelaud, K. Ding, A. Ishii, A. Tanaka, N. Sawada, K. Kudo, M. Senda, Chem. Eur. J. 2001, 7, 730-737. OR/RIU HPLC:
-
Circular dichroism/ultraviolet (CD/UV) or optical rotation/refractive index unit (OR/RIU) HPLC spectroscopy to determine the enantiomeric excesses of products: a) K. Mikami, R. Angelaud, K. Ding, A. Ishii, A. Tanaka, N. Sawada, K. Kudo, M. Senda, Chem. Eur. J. 2001, 7, 730-737. OR/RIU HPLC:
-
-
-
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53
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0034034632
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b) R. Angelaud, Y. Matsumoto, T. Korenaga, K. Kudo, M. Senda, K. Mikami, Chirality. 2000, 544-547.
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Chirality
, pp. 544-547
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Angelaud, R.1
Matsumoto, Y.2
Korenaga, T.3
Kudo, K.4
Senda, M.5
Mikami, K.6
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54
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34250641542
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CD/UV HPLC: c K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523;
-
CD/UV HPLC: c) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523;
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55
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0033557464
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Angew. Chem. Int. Ed. 1999, 38, 497-501;
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Chem. Int. Ed
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Chirality
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Reetz, M.T.1
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e) L. Xu, X. Shen, C. Zhang, K. Mikami, Chirality. 2005, 17, 476-480;
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Chirality
, vol.17
, pp. 476-480
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Xu, L.1
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Eds, K. Nakanishi, N. Berova, R. W. Woody, VCH, Weinheim
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f) P. Salvadori, C. Bertucci, C. Rosini in Circular Dichroism: Principles and Application (Eds.: K. Nakanishi, N. Berova, R. W. Woody), VCH, Weinheim, 1994, p. 541;
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Circular Dichroism: Principles and Application
, pp. 541
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Salvadori, P.1
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g) C. Bertucci, P. Salvadori, L. F. L. Guimaraes, J. Chromatogr. 1994, 666, 535-539;
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h) P. Salvadori, C. Bertucci, C. Rosini, Chirality 1991, 3, 376-385;
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, vol.3
, pp. 376-385
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Salvadori, P.1
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a) E. L. Eliel, S. R. Wilen, L. N. Mander, Stereochemistry of Organic Compounds, Academic Press, New York, 1988, ch. 13;
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Eliel, E.L.1
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b) W. Klyne, J. Buckingham, Atlas of Stereochemistry, Absolute Configurations of Organic Molecules, Fletcher and Son, London, 1978, vol. 2, ch. A′;
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Atlas of Stereochemistry, Absolute Configurations of Organic Molecules, Fletcher and Son
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Thieme, Stuttgart
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c) H. B. Kagan, Stereochemistry, Fundamentals and Methods, Thieme, Stuttgart, 1977, vol. 1-4;
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d) W. Klyne, J. Buckingham, Atlas of Stereochemistry, Absolute Configurations of Organic Molecules, Fletcher and Son, London, 1974, ch. D;
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Atlas of Stereochemistry, Absolute Configurations of Organic Molecules, Fletcher and Son
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Klyne, W.1
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b) I. Linhart, I. Gut, J. Smejkal, J. Novak, Chem. Res. Toxicol. 2000, 13, 36-44.
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, pp. 36-44
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a) A. Ishii, J. Kojima, K. Mikami, Org. Lett. 1999, 1, 2013-2016;
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J. Org. Chem
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Ishii, A.1
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d) N. Gathergood, W. Zhuang, K. A. Jorgensen, J. Am. Chem. Soc. 2000, 122, 12517-12522;
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J. Am. Chem. Soc
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Gathergood, N.1
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e) W. Zhuang, N. Gathergood, R. G. Hazell, K. A. Jorgensen, J. Org. Chem. 2001, 66, 1009-1013;
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J. Org. Chem
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Zhuang, W.1
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f) Y. Yuan, X. Wang, X. Li, K. Ding, J. Org. Chem. 2004, 69, 146-149.
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