86031-03-0Relevant articles and documents
Synthesis and Biological activity of new HMG-CoA reductase inhibitors. 3.1,2 lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids
Jendralla,Granzer,V Kerekjarto,Krause,Schacht,Baader,Bartmann,Beck,Bergmann,Kessler,Wess,Chen,Granata,Herchen,Kleine,Schussler,Wagner
, p. 2962 - 2983 (2007/10/02)
A group of 43 optically active sodium carboxylates (11a-qq and the corresponding lactones 4 were prepared from respective phenols 8 according to Schemes I-III. Phenols 8 were synthesized from commercially available compounds according to Schemes IV-IX. A
MEVINIC ACIDS AND ANALOGUES: PREPARATION OF A KEY CHIRAL INTERMEDIATE
Yang, Yuh-Lin,Falck, J.R.
, p. 4305 - 4308 (2007/10/02)
The preparation of methyl 3-O-tert-butyldiphenylsilyl-2,4-dideoxy-β-D-erytrohexopyranoside, a key chiral intermediate for mevinic acids, and its elaboration into four mevinate analogues are described.