123492-49-9

Upstream product

• 113240-61-2 1,1-Dimethylethyl (S)-5-hydroxy-3-oxo-6-(triphenylmethoxy)hexanoate 
• 123477-28-1 1,1-Dimethylethyl (3R,5S)-3,5-dihydroxy-6-(triphenylmethoxy)hexanoate 
• 150942-98-6 t-butyl lithioacetate 
• 123477-29-2 1,1-Dimethylethyl (3R,5S)-3,5-di-[(1',1'-dimethylethyl)-diphenylsilyloxy]-6-(triphenylmethoxy)hexanoate 
• 113240-61-2 (R)-5-Hydroxy-3-oxo-6-trityloxy-hexanoic acid tert-butyl ester 
• 123477-28-1 (3R,5R)-3,5-Dihydroxy-6-trityloxy-hexanoic acid tert-butyl ester 
• 123477-29-2 (3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-6-trityloxy-hexanoic acid tert-butyl ester 
• 123477-28-1 (3S,5R)-3,5-Dihydroxy-6-trityloxy-hexanoic acid tert-butyl ester 
• 123477-29-2 (3S,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-6-trityloxy-hexanoic acid tert-butyl ester 

Downstream Products

• 116168-28-6 (3S,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-6-oxo-hexanoic acid tert-butyl ester 
• 130852-64-1 (3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-6-oxo-hexanoic acid tert-butyl ester 
• 123477-30-5 1,1-Dimethylethyl (3R,5S)-3,5-di-[(1',1'-dimethylethyl)-diphenylsilyloxy]-6-oxohexanoate 

Relevant academic research and scientific papers

A Highly Stereoselective Route to the Four Stereoisomers of a Six-Carbon Synthon

The syntheses of chiral synthones 13-16 are described utilizing the chiral pool approach starting from either S- or R-malic acid.

Pyrimidinyl-substituted hydroxyacids, lactones and esters and pharmaceutical compositions containing them

Compounds of formula I wherein R1, R2, Q, X and Y have various significances,in free acid form, or in the form of an ester or δ-lactone thereof, or in salt form as appropriate, are described. They are indicated for use as hypolipoproteinemic and anti-athe