136006-57-0

Upstream product

• 2719-27-9 cyclohexanylcarbonyl chloride 
• 110772-22-0 2(RS)-methoxy-4(R)-(tert-butyldiphenylsiloxy)-6(S)-<<(p-tolylsulfonyl)oxy>methyl>tetrahydropyran 
• 86031-03-0 2(RS)-methoxy-4(R)-(tert-butyldiphenylsilyloxy)-6(S)-(iodomethyl)tetrahydropyran 
• 136007-81-3 2,4-dimethyl-6-(cyclohexylhydroxymethyl)phenol 
• 115807-77-7 2,4-dimethyl-6-(cyclohexylcarbonyl)phenol 
• 136007-80-2 1-<(cyclohexylcarbonyl)oxy>-2,4-dimethylbenzene 
• 110772-23-1 [(2S,4R)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-methanol 
• 20654-46-0 2,2-dimethylbutyronitrile 
• 136006-73-0 N-{(S)-Cyclohexyl-[2-((2S,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-ylmethoxy)-3,5-dimethyl-phenyl]-methyl}-2,2-dimethyl-butyramide 
• 105-67-9 2,4-Xylenol 
• 136007-84-6 4(R)-(tert-butyldiphenylsiloxy)-6(S)-<<2,4-dimethyl-6-(cyclohexylhydroxymethyl)phenoxy>methyl>tetrahydropyran-2-one 
• 136007-82-4 {2-[(2S,4R)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-ylmethoxy]-3,5-dimethyl-phenyl}-cyclohexyl-methanol 
• 136007-83-5 (4R,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-[2-(cyclohexyl-hydroxy-methyl)-4,6-dimethyl-phenoxymethyl]-tetrahydro-pyran-2-ol 
• 136007-88-0 4(R)-(tert-butyldiphenylsiloxy)-6(S)-<<2,4-dimethyl-6-phenoxy>methyl>tetrahydropyran-2-one 

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