111392-98-4

Upstream product

• 89956-14-9 [3-(2-Benzyloxyethyl)oxiran-2-yl]methanol 
• 89923-31-9 (E)-5-(benzyloxy)pent-2-en-1-ol 
• 111392-97-3 (S)-5-(tert-Butyl-dimethyl-silanyloxy)-pentane-1,3-diol 
• 3393-45-1 5,6-dihydro-pyran-2-one 
• 111466-32-1 (2S,3R)-4-t-butyldimethylsilyloxy-2,3-epoxy-pentan-1-ol 
• 81096-97-1 (2R,4R)-6-Benzyloxy-hexane-1,2,4-triol 
• 100-39-0 benzyl bromide 
• 203316-24-9 5-phenylmethoxy-1-(tetrahydropyran-2'-yloxy)pent-2-yne 
• 22273-79-6 5-benzyloxy-2-pentyn-1-ol 
• 22273-77-4 ((but-3-yn-1-yloxy)methyl)benzene 
• 38996-32-6 5-(tetrahydropyran-2-yloxy)-3-pentyn-1-ol 
• 81132-13-0 (S)-5-phenylmethoxypentane-1,3-diol 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 111392-99-5 ((S)-5-Benzyloxy-3-methoxymethoxy-pentyloxy)-tert-butyl-dimethyl-silane 
• 86117-01-3 (4R,6R)-(+)-4-hydroxy-6-(2-phenylethyl)-tetrahydro-2H-pyran-2-one 
• 111393-00-1 (S)-5-Benzyloxy-3-methoxymethoxy-pentanal 
• 111393-02-3 (R)-5-Acetoxy-3-methoxymethoxy-7-phenyl-heptanoic acid 
• 111393-01-2 Acetic acid (S)-5-benzyloxy-3-methoxymethoxy-1-phenethyl-pentyl ester 
• 111466-34-3 3β-hydroxy-5β-<(2-phenyl)ethyl>-δ-lactone 
• 203316-44-3 Acetic acid (R)-5-benzyloxy-3-methoxymethoxy-pentyl ester 
• 203316-39-6 (R)-5-Benzyloxy-3-methoxymethoxy-pentanoic acid methyl ester 
• 203316-38-5 (R)-5-Benzyloxy-3-methoxymethoxy-pentanoic acid 
• 203316-34-1 (S)-3-methoxymethoxy-5-phenylmethoxypentan-1-ol 
• 203316-23-8 Acetic acid (R)-1-(2-benzyloxy-ethyl)-3-(tert-butyl-dimethyl-silanyloxy)-propyl ester 

Relevant academic research and scientific papers

Pigments of fungi. XLIV* synthesis of differentially protected chiral pentane-1,3,5-triol derivatives; confirmation of the absolute configuration of naturally occurring 3-acetoxy-2,3-dihydropiptoporic acid

(R)-1-t-Butyldimethylsilyloxy-5-phenylmethoxypentan-3-ol (25), prepared in 68% yield and >99.9% enantiomeric excess over six steps from commercially available but-3-yn-1-ol by Katsuki-Sharpless epoxidation, was converted by way of its 3-methoxymethyl ethe

STUDIES ON ASYMMETRIC SYNTHESIS OF β-HYDROXY-δ-LACTONE INHIBITORS OF HMGCoA REDUCTASE 1. A NEW PREPARATION OF THE LACTONE MOIETY OF COMPACTIN

A new strategy for the preparation of chiral β-hydroxy-δ-lactone inhibitors of HMGCoA reductase is outlined: in particular the compactin lactone moiety has been elaborated by asymmetric epoxidation of the appropriate allylic alcohol and subsequent introdu

Synthesis of Saccharides and Related Polyhydroxylated Natural Products. 2. Simple Deoxyalditols

Asymmetric epoxidation of allylic alcohols followed by selective hydride reduction provides a new route to chiral 1,3-diols and 1,3,5-triols; one of the 1,3,5-triols (21) is also synthesized from D-glucose.