136006-76-3

Upstream product

• 136007-21-1 tert-Butyl-[(2S,4R)-2-(3-cyclohexylmethyl-5-isopropyl-biphenyl-4-yloxymethyl)-6-methoxy-tetrahydro-pyran-4-yloxy]-diphenyl-silane 
• 136007-48-2 (4R,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-(3-cyclohexylmethyl-5-isopropyl-biphenyl-4-yloxymethyl)-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 
• 136007-92-6 3-(cyclohexylmethyl)-5-isopropyl-4-nitrobiphenyl 
• 136007-93-7 3-(cyclohexylmethyl)-5-isopropyl-4-aminobiphenyl 
• 136007-13-1 2-(cyclohexylmethyl)-4-phenyl-6-isopropylphenol 
• 127502-68-5 3-isopropyl-4-nitrobiphenyl 
• 110772-23-1 [(2S,4R)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-methanol 
• 92-93-3 1-phenyl-4-nitrobenzene 
• 136007-63-1 (4R,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-(3-cyclohexylmethyl-5-isopropyl-biphenyl-4-yloxymethyl)-tetrahydro-pyran-2-one 

Downstream Products

• 136006-61-6 Sodium; (3R,5S)-6-(3-cyclohexylmethyl-5-isopropyl-biphenyl-4-yloxy)-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