메뉴 건너뛰기




Volumn , Issue 5, 2008, Pages 840-846

Highly enantioselective hydrogenation of ethyl 5,5-dimethoxy-3- oxopentanoate and its application for the synthesis of a statin precursor

Author keywords

keto esters; Asymmetric catalysis; Hydrogenation; Rhodium; Rosuvastatin; Ruthenium; Statins; Stereoselectivity

Indexed keywords


EID: 46049114957     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200701059     Document Type: Article
Times cited : (19)

References (44)
  • 1
    • 0003445429 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • Ed, I. Ojima, Wiley-VCH, New York
    • Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, New York, 2000.
    • (2000) Catalytic Asymmetric Synthesis
  • 3
    • 0000701744 scopus 로고    scopus 로고
    • 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
  • 5
    • 0005185360 scopus 로고    scopus 로고
    • 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
  • 25
    • 53649096130 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 29
    • 33748358833 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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.
  • 36
    • 53649083352 scopus 로고    scopus 로고
    • 2 pressure of 50 bar.
    • 2 pressure of 50 bar.
  • 42
    • 53649092276 scopus 로고    scopus 로고
    • 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.