-
1
-
-
77149164434
-
-
Andrews, I.; Cui, J.; DaSilva, J.; Dudin, L.; Dunn, P.; Hayler, J.; Hinkley, B.; Hughes, D.; Kaptein, B.; Lorenz, K.; Mathew, S.; Rammeloo, T.; Wang, L.; Wells, A.; White, T.; Zhang, F. Org. Process Res. Dev. 2010, 14, 19-29
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 19-29
-
-
Andrews, I.1
Cui, J.2
Dasilva, J.3
Dudin, L.4
Dunn, P.5
Hayler, J.6
Hinkley, B.7
Hughes, D.8
Kaptein, B.9
Lorenz, K.10
Mathew, S.11
Rammeloo, T.12
Wang, L.13
Wells, A.14
White, T.15
Zhang, F.16
-
3
-
-
79957469767
-
Modern biocatalysis
-
For some book reviews, see: Fessner, W.-D.; Anthonsen, T., Eds.; Wiley-VCH: Weinheim
-
For some book reviews, see: Modern Biocatalysis. Stereoselective and Environmentally Friendly Reactions; Fessner, W.-D.; Anthonsen, T., Eds.; Wiley-VCH: Weinheim, 2009.
-
(2009)
Stereoselective and Environmentally Friendly Reactions
-
-
-
6
-
-
77955686028
-
-
For some recent reviews, see
-
For some recent reviews, see
-
-
-
-
7
-
-
76449120234
-
-
Lee, J. H.; Han, K.; Kim, M.-J.; Park, J. Eur. J. Org. Chem. 2010, 999-1015
-
(2010)
Eur. J. Org. Chem.
, pp. 999-1015
-
-
Lee, J.H.1
Han, K.2
Kim, M.-J.3
Park, J.4
-
9
-
-
39649107133
-
-
Ahn, Y.; Ko, S.-B.; Kim, M.-J.; Park, J. Coord. Chem. Rev. 2008, 252, 647-658
-
(2008)
Coord. Chem. Rev.
, vol.252
, pp. 647-658
-
-
Ahn, Y.1
Ko, S.-B.2
Kim, M.-J.3
Park, J.4
-
11
-
-
33846184753
-
-
For some specific examples, see:
-
For some specific examples, see: Stirling, M.; Blacker, J.; Page, M. I. Tetrahedron Lett. 2007, 48, 1247-1250
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 1247-1250
-
-
Stirling, M.1
Blacker, J.2
Page, M.I.3
-
13
-
-
63749090004
-
-
Thalén, L. K.; Zhao, D.; Sortais, J.-B.; Paetzold, J.; Hoben, C.; Bäckvall, J.-E. Chem.-Eur. J. 2009, 15, 3403-3410
-
(2009)
Chem.-Eur. J.
, vol.15
, pp. 3403-3410
-
-
Thalén, L.K.1
Zhao, D.2
Sortais, J.-B.3
Paetzold, J.4
Hoben, C.5
Bäckvall, J.-E.6
-
14
-
-
77955673693
-
-
For a recent example using Pd-nanoparticles, see
-
For a recent example using Pd-nanoparticles, see
-
-
-
-
15
-
-
73149087689
-
-
Choi, Y.-K.; Kim, Y.; Han, K.; Park, J.; Kim, M.-J. J. Org. Chem. 2009, 74, 9543-9545
-
(2009)
J. Org. Chem.
, vol.74
, pp. 9543-9545
-
-
Choi, Y.-K.1
Kim, Y.2
Han, K.3
Park, J.4
Kim, M.-J.5
-
16
-
-
77955688043
-
-
DKR of secondary heterocyclic amines as proline and pipecolic acid methyl esters
-
DKR of secondary heterocyclic amines as proline and pipecolic acid methyl esters
-
-
-
-
17
-
-
0347595438
-
-
Liljeblad, A.; Kiviniemi, A.; Kanerva, L. T. Tetrahedron 2004, 60, 671-677
-
(2004)
Tetrahedron
, vol.60
, pp. 671-677
-
-
Liljeblad, A.1
Kiviniemi, A.2
Kanerva, L.T.3
-
18
-
-
77955695842
-
-
In this case, a protease was used as catalyst for the acylation
-
In this case, a protease was used as catalyst for the acylation
-
-
-
-
19
-
-
64249095580
-
-
El Blidi, L.; Nechab, M.; Vanthuyne, N.; Gastaldi, S.; Bertrand, M. P.; Gil, G. J. Org. Chem. 2009, 74, 2901-2903
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2901-2903
-
-
El Blidi, L.1
Nechab, M.2
Vanthuyne, N.3
Gastaldi, S.4
Bertrand, M.P.5
Gil, G.6
-
20
-
-
77955702227
-
-
DKR of 8-amino-5,6,7,8-tetrahydroquinoline
-
DKR of 8-amino-5,6,7,8-tetrahydroquinoline
-
-
-
-
21
-
-
33846191192
-
-
Crawford, J. B.; Skerlj, R. T.; Bridger, G. J. J. Org. Chem. 2007, 72, 669-671
-
(2007)
J. Org. Chem.
, vol.72
, pp. 669-671
-
-
Crawford, J.B.1
Skerlj, R.T.2
Bridger, G.J.3
-
22
-
-
77955696035
-
-
For some reviews, see
-
For some reviews, see
-
-
-
-
23
-
-
68949116176
-
-
González-Sabín, J.; Rebolledo, F.; Gotor, V. Chem. Soc. Rev. 2009, 38, 1916-1925
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 1916-1925
-
-
González-Sabín, J.1
Rebolledo, F.2
Gotor, V.3
-
26
-
-
33745110538
-
-
Kotti, S. R. S. S.; Timmons, C.; Li, G. Chem. Biol. Drug Res. 2006, 67, 101-114
-
(2006)
Chem. Biol. Drug Res.
, vol.67
, pp. 101-114
-
-
Kotti, S.R.S.S.1
Timmons, C.2
Li, G.3
-
27
-
-
0032538362
-
-
Lucet, D.; Le Gall, T.; Mioskowski, C. Angew. Chem., Int. Ed. 1998, 37, 2580-2627
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 2580-2627
-
-
Lucet, D.1
Le Gall, T.2
Mioskowski, C.3
-
29
-
-
4043128740
-
-
Govindaraju, T.; Kumar, V. A.; Ganesh, K. N. J. Org. Chem. 2004, 69, 5725-5734
-
(2004)
J. Org. Chem.
, vol.69
, pp. 5725-5734
-
-
Govindaraju, T.1
Kumar, V.A.2
Ganesh, K.N.3
-
30
-
-
77955688851
-
-
N2 displacement of the mesylate group by the carbonyl oxygen of the Boc group
-
N2 displacement of the mesylate group by the carbonyl oxygen of the Boc group
-
-
-
-
32
-
-
77955671563
-
-
Thus far, CAL-B (Novozyme SP-435) has proven to be the most effective catalyst for the aminolysis reaction in organic solvent. For a review, see
-
Thus far, CAL-B (Novozyme SP-435) has proven to be the most effective catalyst for the aminolysis reaction in organic solvent. For a review, see
-
-
-
-
33
-
-
33744784809
-
-
Gotor-Fernández, V.; Busto, E.; Gotor, V. Adv. Synth. Catal. 2006, 348, 797-812
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 797-812
-
-
Gotor-Fernández, V.1
Busto, E.2
Gotor, V.3
-
34
-
-
20644469267
-
-
Chen, C. S.; Fujimoto, Y.; Girdaukas, G.; Sih, C. J. J. Am. Chem. Soc. 1982, 104, 7294-7299
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 7294-7299
-
-
Chen, C.S.1
Fujimoto, Y.2
Girdaukas, G.3
Sih, C.J.4
-
35
-
-
77955676965
-
-
Program "Selectivity" by
-
Program "Selectivity" by Faber, K.; Hoenig, H. http://www.cis.TUGraz.at/orgc/.
-
-
-
Faber, K.1
Hoenig, H.2
-
36
-
-
0742289584
-
-
González-Sabín, J.; Gotor, V.; Rebolledo, F. Tetrahedron: Asymmetry 2004, 15, 481-488
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 481-488
-
-
González-Sabín, J.1
Gotor, V.2
Rebolledo, F.3
-
37
-
-
77955683826
-
-
CAL-B showed very high enantioselectivity toward the R enantiomer of the ester (ee >97% for the produced (R)-1-phenylethanol). Thus, although a racemic ester was used, CAL-B only catalyzed the reaction with the R enantiomer
-
CAL-B showed very high enantioselectivity toward the R enantiomer of the ester (ee >97% for the produced (R)-1-phenylethanol). Thus, although a racemic ester was used, CAL-B only catalyzed the reaction with the R enantiomer.
-
-
-
-
38
-
-
77955681452
-
-
For some examples in which an acyl migration in 1,2-and 1,3-diol monoacetates has been taken advantage of in dynamic asymmetric transformations, see
-
For some examples in which an acyl migration in 1,2-and 1,3-diol monoacetates has been taken advantage of in dynamic asymmetric transformations, see
-
-
-
-
39
-
-
33645856499
-
-
Edin, M.; Martín-Matute, B.; Bäckvall, J.-E. Tetrahedron: Asymmetry 2006, 17, 708-715
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 708-715
-
-
Edin, M.1
Martín-Matute, B.2
Bäckvall, J.-E.3
-
40
-
-
1942469515
-
-
Edin, M.; Steinreiber, J.; Bäckvall, J.-E. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 5761-5766
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 5761-5766
-
-
Edin, M.1
Steinreiber, J.2
Bäckvall, J.-E.3
-
41
-
-
77955698458
-
-
For an example of acid-promoted migration of an ethoxycarbonyl group to an aziridine nitrogen, see
-
For an example of acid-promoted migration of an ethoxycarbonyl group to an aziridine nitrogen, see
-
-
-
-
43
-
-
77955693332
-
-
The addition of only acetic acid (1 equiv) caused the precipitation of the acetate of 5b, and its ee remained unaltered
-
The addition of only acetic acid (1 equiv) caused the precipitation of the acetate of 5b, and its ee remained unaltered.
-
-
-
-
44
-
-
33751499686
-
-
Kazlauskas, R. J.; Weissfloch, A. N. E.; Rappaport, A. T.; Cuccia, L. A. J. Org. Chem. 1991, 56, 2656-2665
-
(1991)
J. Org. Chem.
, vol.56
, pp. 2656-2665
-
-
Kazlauskas, R.J.1
Weissfloch, A.N.E.2
Rappaport, A.T.3
Cuccia, L.A.4
|