110705-72-1

Upstream product

• 2719-27-9 cyclohexanylcarbonyl chloride 
• 105-67-9 2,4-Xylenol 
• 110772-23-1 [(2S,4R)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-methanol 
• 110724-61-3 (4R,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-(2-cyclohexylmethyl-4,6-dimethyl-phenoxymethyl)-tetrahydro-pyran-2-one 
• 110723-90-5 tert-Butyl-[(2S,4R)-2-(2-cyclohexylmethyl-4,6-dimethyl-phenoxymethyl)-6-methoxy-tetrahydro-pyran-4-yloxy]-diphenyl-silane 
• 136007-43-7 (4R,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-(2-cyclohexylmethyl-4,6-dimethyl-phenoxymethyl)-tetrahydro-pyran-2-ol 
• 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 
• 115807-77-7 2,4-dimethyl-6-(cyclohexylcarbonyl)phenol 
• 136007-80-2 1-<(cyclohexylcarbonyl)oxy>-2,4-dimethylbenzene 
• 2162-61-0 2-Cyclohexylmethyl-4,6-dimethyl-phenol 

Downstream Products

• 136006-54-7 Sodium; (3R,5S)-6-(2-cyclohexylmethyl-4,6-dimethyl-phenoxy)-3,5-dihydroxy-hexanoate 

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