54551-71-2

Upstream product

• 38469-73-7 1-(4-hydroxyphenyl)-2-phenylethan-1,2-dione 
• 100-58-3 phenylmagnesium bromide 
• 99967-27-8 (trimethylsiloxy)<(4-trimethylsiloxy)phenyl>acetonitrile 
• 120743-99-9 p-[(tert-butyldimethylsilyl)oxy]benzaldehyde 
• 1569272-10-1 (2-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1,3-dithian-2-yl)(phenyl)methanol 
• 1569271-87-9 1-(4-((tert-butyldimethylsilyl)oxy)phenyl)-2-hydroxy-2-phenylethanone 
• 156262-17-8 (4-(1,3-dithian-2-yl)phenoxy)(tert-butyl)dimethylsilane 
• 100-52-7 benzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 1569271-88-0 4-(2-hydroxy-2-phenylacetyl)phenyl acetate 
• 1569271-70-0 ethyl 2-(4-acetoxyphenyl)-2-phenylacetate 
• 38469-73-7 1-(4-hydroxyphenyl)-2-phenylethan-1,2-dione 

Relevant academic research and scientific papers

Reduction of Unsymmetrical Benzils Using Sodium Dithionite

Contrary to a previous report, reduction of unsymmetrical benzils by sodium dithionite (sodium hydrosulfite) in general yields a mixture of isomeric benzoins.Whereas the reduction of aldehydes and ketones by dithionite apparently takes place by a nucleophilic addition mechanism, the reduction of benzils proceeds by an electron-transfer mechanism.The initial product of the reduction is the (Z)-α,α'-stilbenediol which is produced stereospecifically.The ultimate benzoin products, then, result from the two different modes of ketolization of the stilbenediol intermediate.

Synthesis of hydroxy benzoin/benzil analogs and investigation of their antioxidant, antimicrobial, enzyme inhibition, and cytotoxic activities

In this study, hydroxy benzoin (1-7), benzil (8-14), and benzoin/benzil-O-β-D-glucosides (15-25) were synthesized to investigate their biological activities. An efficient method for synthesizing hydroxy benzoin compounds (1-7) was prepared from four diffe

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

Chromophoric photocrosslinking compound

A photoactive compound that is the reaction product of an alkenyl azlactone compound and a nucleophilic aromatic ketone is described. Mer units derived from this compound can be used, for example, to crosslink via a hydrogen abstracting mechanism acrylic polymers in which they are incorporated.