The synthesis of a new 3-hydroxy-3-methylglutaryl coenzyme A reduc-----tase inhibitor starting from 4,4' -difluorobenzophenone is described. Mevinolin 1 and its congeners are potent inhibitors of 3-hydroxy-3-methyl-
A diastereospecific, non-racemic synthesis of a novel β-hydroxy-δ-lactone HMG-CoA reductase inhibitor
✍ Scribed by M. Sletzinger; T.R. Verhoeven; R.P. Volante; J.M. McNamara; E.G. Corley; T.M.H. Liu
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 232 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The coupling of acyl anion equivalent 12b with chiral synthon 14, derived from isoascorbic acid, and a highly stereospecific reduction of the resulting e-Tydroxy ketone 3 highlight an efficient synthesis of 8-hydroxy-&lactone 2.
📜 SIMILAR VOLUMES
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A series of S-lactone (1 and Z), oxetane (3) and azetidinone (4 and 5) analogs were prepared from the HMG CoA synthase inhibitor L-659.699 ((E,E)-ll-[3'R-~ydymethyl)-4'-oxo-2'R-oxetanyl]-3,5,7Rtrimethyl-2,4-undecadienoic acid1v2), which maintained the truns relationship of the ring side chains. The