136007-22-2

Upstream product

• 352-13-6 4-flourophenylmagnesium bromide 
• 136007-96-0 α-formyl-γ--β-naphthol 
• 136007-95-9 γ--β-naphthol 
• 110772-23-1 [(2S,4R)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-methanol 
• 82378-95-8 γ--β-naphthol 
• 883-99-8 3-hydroxy-2-naphthoic acid methyl ester 
• 86031-03-0 2(RS)-methoxy-4(R)-(tert-butyldiphenylsilyloxy)-6(S)-(iodomethyl)tetrahydropyran 
• 136007-15-3 2-isopropyl-4--4b-naphthol 
• 110772-22-0 2(RS)-methoxy-4(R)-(tert-butyldiphenylsiloxy)-6(S)-<<(p-tolylsulfonyl)oxy>methyl>tetrahydropyran 

Downstream Products

• 136006-64-9 Sodium; (3R,5S)-6-{3-[bis-(4-fluoro-phenyl)-methyl]-1-isopropyl-naphthalen-2-yloxy}-3,5-dihydroxy-hexanoate 
• 136007-64-2 (4R,6S)-6-{3-[Bis-(4-fluoro-phenyl)-methyl]-1-isopropyl-naphthalen-2-yloxymethyl}-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-one 
• 136006-77-4 (4R,6S)-6-{3-[Bis-(4-fluoro-phenyl)-methyl]-1-isopropyl-naphthalen-2-yloxymethyl}-4-hydroxy-tetrahydro-pyran-2-one 
• 136007-51-7 (4R,6S)-6-{3-[Bis-(4-fluoro-phenyl)-methyl]-1-isopropyl-naphthalen-2-yloxymethyl}-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-ol 

Relevant academic research and scientific papers

Synthesis and Biological activity of new HMG-CoA reductase inhibitors. 3.1,2 lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids

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