## Abstract A new synthetic method for the preparation of pitavastatin is described. The approach circumvents various synthetic problems associated with the buildup of the 3,5βdihydroxyβC~7~ acid side chain of HMGβCoA reductase inhibitors (statins). The use of the C~6~βamide derivative **5** instea
A New and Efficient Synthesis of the HMG-CoA Reductase Inhibitor Pitavastatin
β Scribed by Murat Acemoglu; Andre Brodbeck; Angel Garcia; Dominique Grimler; Marc Hassel; Bernhard Riss; Robert Schreiber
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- German
- Weight
- 23 KB
- Volume
- 90
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
On p. 1074, in Scheme 3, the correct formula of NK-104 should be as follows:
- On p. 1077, line 16 should read as follows:
(390 ml) was cooled to Γ 788, and 1.6m BuLi in hexane (374.4 g, 881 mmol) was added under 3) On p. 1078, line 15 should read as follows:
As HPLC revealed the presence of more than 10% of 8 in the mixture, 5 (21.17 g, 44.9 mmol) and K 2 CO 3
π SIMILAR VOLUMES
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The absorption and disposition of fluvastatin have been studied in the female rabbit. In naive rabbits receiving a single oral dose (1 mg kg-I) of [3H]fluvastatin, absorption was rapid and amounted to c. 90 per cent compared with an intravenous reference dose. The drug was subject to considerable fi