-
13
-
-
33846289229
-
-
D. Pei, Z. Wang, S. Wei, Y. Zhang, and J. Sun Org. Lett. 8 2006 5913
-
(2006)
Org. Lett.
, vol.8
, pp. 5913
-
-
Pei, D.1
Wang, Z.2
Wei, S.3
Zhang, Y.4
Sun, J.5
-
15
-
-
53849138558
-
-
D. Pei, Y. Zhang, S. Wei, M. Wang, and J. Sun Adv. Synth. Catal. 350 2008 619
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 619
-
-
Pei, D.1
Zhang, Y.2
Wei, S.3
Wang, M.4
Sun, J.5
-
16
-
-
34247120129
-
-
For a review on asymmetric Michael additions of thiols, see: Enders, D.; Luettgen, K.; Narine, A. A. Synthesis 2007, 7, 959. For organocatalytic enantioselective Michael additions of sulfur nucleophiles to α,β-unsaturated carbonyl compounds, see
-
(2007)
Synthesis
, vol.7
, pp. 959
-
-
Enders, D.1
Luettgen, K.2
Narine, A.A.3
-
17
-
-
62849091903
-
-
Y. Liu, B. Sun, B. Wang, M. Wakem, and L. Deng J. Am. Chem. Soc. 131 2009 418
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 418
-
-
Liu, Y.1
Sun, B.2
Wang, B.3
Wakem, M.4
Deng, L.5
-
20
-
-
38549126717
-
-
For metal-catalyzed enantioselective Michael additions of sulfur nucleophiles to α,β-unsaturated carbonyl compounds, see
-
P. Ricci, A. Carlone, G. Bartoli, M. Bosco, L. Sambri, and P. Melchiorre Adv. Synth. Catal. 350 2008 49 For metal-catalyzed enantioselective Michael additions of sulfur nucleophiles to α,β-unsaturated carbonyl compounds, see
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 49
-
-
Ricci, P.1
Carlone, A.2
Bartoli, G.3
Bosco, M.4
Sambri, L.5
Melchiorre, P.6
-
28
-
-
77953489540
-
-
Y.-H. Hui, J. Jiang, W.-T. Wang, W.-L. Chen, Y.-F. Cai, L.-L. Lin, X.-H. Liu, and X.-M. Feng Angew. Chem., Int. Ed. 49 2010 4290
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 4290
-
-
Hui, Y.-H.1
Jiang, J.2
Wang, W.-T.3
Chen, W.-L.4
Cai, Y.-F.5
Lin, L.-L.6
Liu, X.-H.7
Feng, X.-M.8
-
29
-
-
80455178516
-
-
X. Tian, C. Cassani, Y. Lium, A. Moran, A. Urakawa, P. Galzerano, E. Arceo, and P. Melchiorre J. Am. Chem. Soc. 133 2011 17934
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 17934
-
-
Tian, X.1
Cassani, C.2
Lium, Y.3
Moran, A.4
Urakawa, A.5
Galzerano, P.6
Arceo, E.7
Melchiorre, P.8
-
31
-
-
0000437812
-
-
To obtain a reasonable ee (58%), stoichiometric cinchona alkaloid catalyst was required
-
N. Kobayashi, and K. Iwai J. Org. Chem. 46 1981 1823 To obtain a reasonable ee (58%), stoichiometric cinchona alkaloid catalyst was required
-
(1981)
J. Org. Chem.
, vol.46
, pp. 1823
-
-
Kobayashi, N.1
Iwai, K.2
-
35
-
-
0023760272
-
-
Azole antifungals, such as sulconazole are known to act by inhibition of the fungal cell CYP51 lanosterol demethylase. Though inhibitory activity data for the enantiomers of sulconazole is not available, in vitro studies of very similar azole antifungals have demonstrated that the R-enantiomer can be up to 60-fold more active than the S-enantiomer. For biological data on azole enantiomers, see
-
R.A. Fromtling Clin. Microbiol. Rev. 1 1988 187 Azole antifungals, such as sulconazole are known to act by inhibition of the fungal cell CYP51 lanosterol demethylase. Though inhibitory activity data for the enantiomers of sulconazole is not available, in vitro studies of very similar azole antifungals have demonstrated that the R-enantiomer can be up to 60-fold more active than the S-enantiomer. For biological data on azole enantiomers, see
-
(1988)
Clin. Microbiol. Rev.
, vol.1
, pp. 187
-
-
Fromtling, R.A.1
-
36
-
-
0036245022
-
-
M.G. Quaglia, E. Donati, N. Desideri, S. Fanali, F.D. D'Auria, and M. Tecca Chirality 14 2002 449
-
(2002)
Chirality
, vol.14
, pp. 449
-
-
Quaglia, M.G.1
Donati, E.2
Desideri, N.3
Fanali, S.4
D'Auria, F.D.5
Tecca, M.6
-
37
-
-
0030894125
-
-
D.C. Lamb, D.E. Kelly, B.C. Baldwin, F. Gozzo, P. Boscott, W.G. Richards, and S.L. Kelly FEMS Microbiol. Lett. 149 1997 25
-
(1997)
FEMS Microbiol. Lett.
, vol.149
, pp. 25
-
-
Lamb, D.C.1
Kelly, D.E.2
Baldwin, B.C.3
Gozzo, F.4
Boscott, P.5
Richards, W.G.6
Kelly, S.L.7
-
38
-
-
84862794399
-
-
(Ferrer Internacional S.A., Spain) PCT Appl. WO 03/068770, February 4
-
Foguet, R.; Ramentol, J.; Guglietta, A.; Palacin, C.; Anglada, L. (Ferrer Internacional S.A., Spain) PCT Appl. WO 03/068770, February 4, 2003.
-
(2003)
-
-
Foguet, R.1
Ramentol, J.2
Guglietta, A.3
Palacin, C.4
Anglada, L.5
-
39
-
-
13444270903
-
-
A. Berkessel, F. Cleemann, S. Mukherjee, T.N. Mueller, and J. Lex Angew. Chem., Int. Ed. 44 2005 807
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 807
-
-
Berkessel, A.1
Cleemann, F.2
Mukherjee, S.3
Mueller, T.N.4
Lex, J.5
-
40
-
-
79960517189
-
-
V. Antonucci, J. Coleman, J.B. Ferry, N. Johnson, M. Mathe, J.P. Scott, and J. Xu Org. Process Res. Dev. 15 2011 939
-
(2011)
Org. Process Res. Dev.
, vol.15
, pp. 939
-
-
Antonucci, V.1
Coleman, J.2
Ferry, J.B.3
Johnson, N.4
Mathe, M.5
Scott, J.P.6
Xu, J.7
-
42
-
-
0037189898
-
-
For relevant mechanistic studies of H-bonding organocatalysis, see
-
For relevant mechanistic studies of H-bonding organocatalysis, see: P. Vachal, and E.N. Jacobsen J. Am. Chem. Soc. 124 2002 10012
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 10012
-
-
Vachal, P.1
Jacobsen, E.N.2
-
47
-
-
0037055013
-
-
Z. Han, D. Krishnamurthy, P. Grover, Q.K. Fang, and C.H. Senanayake J. Am. Chem. Soc. 124 2002 7880
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 7880
-
-
Han, Z.1
Krishnamurthy, D.2
Grover, P.3
Fang, Q.K.4
Senanayake, C.H.5
-
48
-
-
28044452665
-
-
C.H. Senanayake, D. Krishnamurthy, Z.-H. Lu, Z. Han, and I. Gallou Aldrichimica Acta 38 2005 93
-
(2005)
Aldrichimica Acta
, vol.38
, pp. 93
-
-
Senanayake, C.H.1
Krishnamurthy, D.2
Lu, Z.-H.3
Han, Z.4
Gallou, I.5
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