-
1
-
-
0003445429
-
-
Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer-Verlag, Berlin
-
Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), vol. I-III, Springer-Verlag, Berlin, 1999;
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.I-III
-
-
-
2
-
-
84891580093
-
-
Ed, I. Ojima, Wiley-VCH, New York
-
Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, New York, 2000.
-
(2000)
Catalytic Asymmetric Synthesis
-
-
-
3
-
-
0000701744
-
-
Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer-Verlag, Berlin
-
a) J. M. Brown, in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer-Verlag, Berlin, 1999, vol. I, pp. 121-182;
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.1
, pp. 121-182
-
-
Brown, J.M.1
-
4
-
-
0002634798
-
-
Ed, I. Ojima, Wiley-VCH, New York
-
b) T. Ohkuma, M. Kitamura, R. Noyori, in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, New York, 2000, pp. 1-110.
-
(2000)
Catalytic Asymmetric Synthesis
, pp. 1-110
-
-
Ohkuma, T.1
Kitamura, M.2
Noyori, R.3
-
5
-
-
0005185360
-
-
Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer-Verlag, Berlin
-
T. Ohkuma, R. Noyori, in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer-Verlag, Berlin, 1999, vol. I, pp. 204-210.
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.1
, pp. 204-210
-
-
Ohkuma, T.1
Noyori, R.2
-
6
-
-
4444320477
-
-
a) O. Labeeuw, D. Blanc, P. Phansavath, V. Ratovelomanana-Vidal, J.-P. Genêt, Eur. J. Org. Chem. 2004, 2352-2358;
-
(2004)
Eur. J. Org. Chem
, pp. 2352-2358
-
-
Labeeuw, O.1
Blanc, D.2
Phansavath, P.3
Ratovelomanana-Vidal, V.4
Genêt, J.-P.5
-
7
-
-
0037556292
-
-
b) V. Ratovelomanana-Vidal, C. Girard, R. Touati, J. P. Tranchier, B. Ben Hassine, J.-P. Genêt, Adv. Synth. Catal. 2003, 345, 261-274;
-
(2003)
Adv. Synth. Catal
, vol.345
, pp. 261-274
-
-
Ratovelomanana-Vidal, V.1
Girard, C.2
Touati, R.3
Tranchier, J.P.4
Ben Hassine, B.5
Genêt, J.-P.6
-
8
-
-
0034605807
-
-
c) O. Poupardin, C. Greck, J.-P. Genêt, Tetrahedron Lett. 2000, 41, 8795-8797.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 8795-8797
-
-
Poupardin, O.1
Greck, C.2
Genêt, J.-P.3
-
9
-
-
33845278216
-
-
a) M. Kitamura, T. Ohkuma, S. Inoue, N. Sayo, H. Kumobayashi, S. Akutagawa, T. Ohta, H. Takaya, R. Noyori, J. Am. Chem. Soc. 1988, 110, 629-631;
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 629-631
-
-
Kitamura, M.1
Ohkuma, T.2
Inoue, S.3
Sayo, N.4
Kumobayashi, H.5
Akutagawa, S.6
Ohta, T.7
Takaya, H.8
Noyori, R.9
-
10
-
-
33845282793
-
-
b) R. Noyori, T. Ohkuma, M. Kitamura, H. Takaya, N. Sayo, H. Kumobayashi, S. Akutagawa, J. Am. Chem. Soc. 1987, 109, 5856-5858;
-
(1987)
J. Am. Chem. Soc
, vol.109
, pp. 5856-5858
-
-
Noyori, R.1
Ohkuma, T.2
Kitamura, M.3
Takaya, H.4
Sayo, N.5
Kumobayashi, H.6
Akutagawa, S.7
-
12
-
-
0034703214
-
-
a) Z. Zhang, H. Qian, J. Longmire, X. Zhang, J. Org. Chem. 2000, 65, 6223-6226;
-
(2000)
J. Org. Chem
, vol.65
, pp. 6223-6226
-
-
Zhang, Z.1
Qian, H.2
Longmire, J.3
Zhang, X.4
-
13
-
-
4444257089
-
-
b) A. Hu, H. L. Ngo, W. Lin, Angew. Chem. Int. Ed. 2004, 43, 2501-2504;
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 2501-2504
-
-
Hu, A.1
Ngo, H.L.2
Lin, W.3
-
14
-
-
0037042288
-
-
c) Y.-G. Zhou, W. Tang, W.-B. Wang, W. Li, X. Zhang, J. Am. Chem. Soc. 2002, 124, 4952-4953.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 4952-4953
-
-
Zhou, Y.-G.1
Tang, W.2
Wang, W.-B.3
Li, W.4
Zhang, X.5
-
15
-
-
0000585749
-
-
M. J. Burk, T. G. P. Harper, C. S. Kalberg, J. Am. Chem. Soc. 1995, 117, 4423-4424.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 4423-4424
-
-
Burk, M.J.1
Harper, T.G.P.2
Kalberg, C.S.3
-
16
-
-
0033605937
-
-
T. Yamano, N. Taya, M. Kawada, T. Huang, T. Imamoto, Tetrahedron Lett. 1999, 40, 2577-2580.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 2577-2580
-
-
Yamano, T.1
Taya, N.2
Kawada, M.3
Huang, T.4
Imamoto, T.5
-
17
-
-
4944250331
-
-
K. Junge, B. Hagemann, S. Enthaler, G. Oehme, M. Michalik, A. Monsees, T. Riermeier, U. Dingerdissen, M. Beller, Angew. Chem. Int. Ed. 2004, 43, 5066-5069.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 5066-5069
-
-
Junge, K.1
Hagemann, B.2
Enthaler, S.3
Oehme, G.4
Michalik, M.5
Monsees, A.6
Riermeier, T.7
Dingerdissen, U.8
Beller, M.9
-
18
-
-
0037083915
-
-
T. Ireland, K. Tappe, G. Grossheimann, P. Knochel, Chem. Eur. J. 2002, 8, 843-852.
-
(2002)
Chem. Eur. J
, vol.8
, pp. 843-852
-
-
Ireland, T.1
Tappe, K.2
Grossheimann, G.3
Knochel, P.4
-
19
-
-
0032543449
-
-
P. J. Pye, K. Rossen, R. A. Reamer, R. P. Volante, P. J. Reider, Tetrahedron Lett. 1998, 39, 4441-4444.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4441-4444
-
-
Pye, P.J.1
Rossen, K.2
Reamer, R.A.3
Volante, R.P.4
Reider, P.J.5
-
20
-
-
34147121393
-
-
a) I. Karamé, E. Bellur, S. Rotzoll, P. Langer, C. Fischer, J. Holz, A. Börner, Synth. Commun. 2007, 37, 1067-1076;
-
(2007)
Synth. Commun
, vol.37
, pp. 1067-1076
-
-
Karamé, I.1
Bellur, E.2
Rotzoll, S.3
Langer, P.4
Fischer, C.5
Holz, J.6
Börner, A.7
-
21
-
-
0034703752
-
-
b) C.-C. Pai, C.-W. Lin, C.-C. Lin, C.-C. Chen, A. S. C. Chan, W. T. Tong, J. Am. Chem. Soc. 2000, 122, 11513-11514;
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 11513-11514
-
-
Pai, C.-C.1
Lin, C.-W.2
Lin, C.-C.3
Chen, C.-C.4
Chan, A.S.C.5
Tong, W.T.6
-
22
-
-
0028343857
-
-
c) J. P. Genêt, C. Pinel, V. Ratovelomanana-Vidal, S. Mallart, X. Pfister, L. Bischoff, M. C. Cano de Andrade, S. Darses, C. Galopin, J. A. Laffitte, Tetrahedron: Asymmetry 1994, 5, 675-690.
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 675-690
-
-
Genêt, J.P.1
Pinel, C.2
Ratovelomanana-Vidal, V.3
Mallart, S.4
Pfister, X.5
Bischoff, L.6
Cano de Andrade, M.C.7
Darses, S.8
Galopin, C.9
Laffitte, J.A.10
-
23
-
-
33846016221
-
-
V. I. Tararov, G. König, A. Börner, Adv. Synth. Catal. 2006, 348, 2633-2644.
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 2633-2644
-
-
Tararov, V.I.1
König, G.2
Börner, A.3
-
24
-
-
33845929620
-
-
V. I. Tararov, N. Andrushko, V. Andrushko, G. König, A. Spannenberg, A. Börner, Eur. J. Org. Chem. 2006, 5543-5550.
-
(2006)
Eur. J. Org. Chem
, pp. 5543-5550
-
-
Tararov, V.I.1
Andrushko, N.2
Andrushko, V.3
König, G.4
Spannenberg, A.5
Börner, A.6
-
25
-
-
53649096130
-
Therefore statins are the most powerful lipid-lowering agents used for reducing cholesterol levels in people with or at risk of cardiovascular disease
-
Atorvastatin belongs to the class of statins that are very effective inhibitors of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase HMGR, Eds: A. Gaw, C. J. Packard, J. Shepherd, Taylor & Francis
-
Atorvastatin belongs to the class of statins that are very effective inhibitors of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase (HMGR). Therefore statins are the most powerful lipid-lowering agents used for reducing cholesterol levels in people with or at risk of cardiovascular disease: Statins, The HMG CoA Reductase Inhibitors in Perspective (Eds: A. Gaw, C. J. Packard, J. Shepherd), Taylor & Francis, 2003.
-
(2003)
Statins, The HMG CoA Reductase Inhibitors in Perspective
-
-
-
26
-
-
14644433290
-
-
For the application of statins for treatment of hypercholesterolemia and hyperlipidaemia see: a, Eds, J.-J. Li, D. S. Johnson, D. R. Sliskovic, B. D. Roth, Wiley-Interscience, New York
-
For the application of statins for treatment of hypercholesterolemia and hyperlipidaemia see: a) Contemporary Drug Synthesis (Eds.: J.-J. Li, D. S. Johnson, D. R. Sliskovic, B. D. Roth), Wiley-Interscience, New York, 2004, pp. 113-123;
-
(2004)
Contemporary Drug Synthesis
, pp. 113-123
-
-
-
28
-
-
21844434482
-
-
c) L. Calza, V. Colangeli, R. Manfredi, G. Legnani, L. Tampellini, D. Pocaterra, F. Chiodo, AIDS 2005, 19, 1103-1105.
-
(2005)
AIDS
, vol.19
, pp. 1103-1105
-
-
Calza, L.1
Colangeli, V.2
Manfredi, R.3
Legnani, G.4
Tampellini, L.5
Pocaterra, D.6
Chiodo, F.7
-
29
-
-
33748358833
-
-
and literature cited therein. For a systematic review about application of statins in the treatment of chronic heart failure see
-
For a systematic review about application of statins in the treatment of chronic heart failure see: P. van der Harst, A. A. Voors, W. H. van Gilst, M. Böhm, D. J. van Veldhuisen, PLoS Med. 2006, 3, e333; and literature cited therein.
-
(2006)
PLoS Med
, vol.3
-
-
van der Harst, P.1
Voors, A.A.2
van Gilst, W.H.3
Böhm, M.4
van Veldhuisen, D.J.5
-
31
-
-
21444433649
-
-
Rosuvastatin was approved as the cholesterol-lowering drug Crestor in August, 2003. More about the application of rosuvastatin see: N. S. Culhane, S. L. Lettieri, J. R. Skae, Pharmacotherapy 2005, 25, 990-1000 and literature cited therein.
-
Rosuvastatin was approved as the cholesterol-lowering drug Crestor in August, 2003. More about the application of rosuvastatin see: N. S. Culhane, S. L. Lettieri, J. R. Skae, Pharmacotherapy 2005, 25, 990-1000 and literature cited therein.
-
-
-
-
32
-
-
53649092840
-
-
Rosuvastatin appears to reduce low-density lipoprotein (LDL) cholesterol to a greater degree than rivals in the class without additional adverse effects. Rosuvastatin is approved for the treatment of elevated LDL cholesterol (dyslipidemia, total cholesterol (hypercholesterolemia) and/or triglycerides hypertriglyceridemia, The main competitor to rosuvastatin is atorvastatin, which is the first totally synthetic HMG-CoA-reductase inhibitor that is marketed as a single enantiomer
-
Rosuvastatin appears to reduce low-density lipoprotein (LDL) cholesterol to a greater degree than rivals in the class without additional adverse effects. Rosuvastatin is approved for the treatment of elevated LDL cholesterol (dyslipidemia), total cholesterol (hypercholesterolemia) and/or triglycerides (hypertriglyceridemia). The main competitor to rosuvastatin is atorvastatin, which is the first totally synthetic HMG-CoA-reductase inhibitor that is marketed as a single enantiomer.
-
-
-
-
35
-
-
84969808662
-
-
D. W. Brooks, L. D.-L. Lu, S. Masamune, Angew. Chem. Int. Ed. Engl. 1979, 18, 72-74.
-
(1979)
Angew. Chem. Int. Ed. Engl
, vol.18
, pp. 72-74
-
-
Brooks, D.W.1
Lu, L.D.-L.2
Masamune, S.3
-
36
-
-
53649083352
-
-
2 pressure of 50 bar.
-
2 pressure of 50 bar.
-
-
-
-
39
-
-
0023897616
-
-
M. Kitamura, T. Ohkuma, H. Takaya, R. Noyori, Tetrahedron Lett. 1988, 29, 1555-1556.
-
(1988)
Tetrahedron Lett
, vol.29
, pp. 1555-1556
-
-
Kitamura, M.1
Ohkuma, T.2
Takaya, H.3
Noyori, R.4
-
40
-
-
0000345787
-
-
A. Togni, C. Breutel, A. Schnyder, F. Spindler, H. Landert, A. Tijani, J. Am. Chem. Soc. 1994, 116, 4062-4066.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 4062-4066
-
-
Togni, A.1
Breutel, C.2
Schnyder, A.3
Spindler, F.4
Landert, H.5
Tijani, A.6
-
41
-
-
0032863340
-
-
G. Franciò, C. G. Arena, F. Faraone, C. Graiff, M. Lanfranchi, A. Tiripicchio, Eur. J. Inorg. Chem. 1999, 8, 1219-1227.
-
(1999)
Eur. J. Inorg. Chem
, vol.8
, pp. 1219-1227
-
-
Franciò, G.1
Arena, C.G.2
Faraone, F.3
Graiff, C.4
Lanfranchi, M.5
Tiripicchio, A.6
-
42
-
-
53649092276
-
-
Unfortunately, it was not possible to increase the yield of (R)-6 higher than noted above.
-
Unfortunately, it was not possible to increase the yield of (R)-6 higher than noted above.
-
-
-
-
43
-
-
46049089700
-
-
following article
-
N. Andrushko, V. Andrushko, G. König, A. Spannenberg, A. Börner, Eur. J. Org. Chem. 2008, 847-853, following article.
-
(2008)
Eur. J. Org. Chem
, pp. 847-853
-
-
Andrushko, N.1
Andrushko, V.2
König, G.3
Spannenberg, A.4
Börner, A.5
-
44
-
-
84889582115
-
-
H. E. Gottlieb, V. Kotlyar, A. Nudelman, J. Org. Chem. 1997, 62, 7512-7515.
-
(1997)
J. Org. Chem
, vol.62
, pp. 7512-7515
-
-
Gottlieb, H.E.1
Kotlyar, V.2
Nudelman, A.3
|