444068-96-6

Upstream product

• 5061-21-2 α-bromo-γ-butyrolactone 
• 103-16-2 4-Benzyloxyphenol 

Downstream Products

• 864541-95-7 2-(4-benzyloxyphenoxy)-4-hydroxy-N-methoxy-N-methylbutyramide 
• 857903-73-2 methyl 2-(4-benzyloxyphenoxy)-4-hydroxybutyrate 
• 857903-48-1 3-(4-hydroxyphenoxy)butyrolactone 
• 864541-99-1 2-(4-benzyloxyphenoxy)-4-hydroxy-1-(pyrrolidin-1-yl)butan-1-one 
• 857903-42-5 methyl 2-(4-benzyloxyphenoxy)-4-p-toluenesulfonylbutyrate 
• 857903-50-5 3-{4-[(7-chloro-2-quinoxalinyl)oxy]phenoxy}butyrolactone 
• 444068-99-9 2-(4-benzyloxyphenoxy)-4-(tert-butyldiphenylsilyloxy)-N-methoxy-N-methylbutyramide 
• 444068-97-7 4-(4-benzyloxyphenoxy)-6-(tert-butyldiphenylsilyloxy)-2-methylhexan-3-one 
• 864542-04-1 2-(4-benzyloxyphenoxy)-2-[2-(tert-butyldiphenylsilyloxy)ethyl]-1-(3,4-dihydro-1H-isoquinolin-2-yl)pent-4-en-1-one 
• 864542-01-8 2-(4-benzyloxyphenoxy)-4-(tert-butyldiphenylsilyloxy)-1-(pyrrolidin-1-yl)butan-1-one 
• 864541-96-8 4-(4-benzyloxyphenoxy)-6-(tert-butyldiphenylsilyloxy)hexan-3-one 
• 864542-03-0 2-(4-benzyloxyphenoxy)-1-(3,4-dihydro-1H-isoquinolin-2-yl)-2-(2-hydroxyethyl)pent-4-en-1-one 
• 864542-02-9 3-allyl-3-(4-benzyloxyphenoxy)dihydrofuran-2-one 

Relevant academic research and scientific papers

Reduction of α-aryloxy carbonyl compounds with samarium(II) iodide. A new traceless linker for the solid phase synthesis of carbonyl compounds

A new linker for the solid phase synthesis of functionalised carbonyl compounds which is cleaved under mild, neutral conditions using samarium(II) iodide has been developed; the manipulation of an immobilised γ-butyrolactone has been carried out to illust

Synthetic modification of the 2-oxypropionic acid moiety in 2-{4-[(7-chloro-2-quinoxalinyl)oxy]phenoxy}propionic acid (XK469), and consequent antitumor effects. Part 4

The criteria for the activity of 2-{4-[(7-chloro-2-quinoxalinyl)oxy] phenoxy}propionic acid (XK469) and 2-{4-[(7-bromo-2-quinolinyl)oxy]phenoxy} propionic acid (SH80) against transplanted tumors in mice established in previous studies, require a (7-halo-2

Evaluation of a new linker system cleaved using samarium(II) iodide. Application in the solid phase synthesis of carbonyl compounds

A new linker design for solid phase synthesis has been developed that is cleaved under mild, neutral conditions using samarium(II) iodide. The feasibility of the linker approach has been illustrated in the solid phase synthesis of ketones and amides using