1569271-72-2

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 54551-72-3 2-(4-chlorophenyl)-2-hydroxy-1-(4-methoxyphenyl)ethan-1-one 
• 122-51-0 orthoformic acid triethyl ester 
• 1569272-02-1 (4-chlorophenyl)(2-(4-methoxyphenyl)-1,3-dithian-2-yl)methanol 
• 24588-72-5 2-(4-methoxyphenyl)-1,3-dithiane 

Relevant academic research and scientific papers

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