875018-27-2

Upstream product

• 96013-95-5 3-(tert-butyl-dimethyl-sylanyloxy)benzaldehyde 
• 214360-76-6 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 121667-78-5 3-(3',4',5'-trimethoxyphenyl)propanal 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 178445-84-6 1-(3-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)-1-propanone 
• 178445-81-3 (E)-1-(3-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 
• 121-71-1 3-Hydroxyacetophenone 
• 53560-26-2 3-(3,4,5-trimethoxyphenyl)propan-1-ol 
• 25173-72-2 3-(3,4,5-trimethoxyphenyl)propanoic acid 
• 902120-02-9 (R)-(+)-3-[1-hydroxy-3-(3,4,5-trimethoxyphenyl)propyl]phenol 
• 902119-94-2 (R)-(+)-1-[3-(tert-butyldimethylsilyloxy)phenyl]-3-(3,4,5-trimethoxyphenyl)propan-1-ol 
• 902119-93-1 1-[3-(tert-butyldimethylsilyloxy)phenyl]-3-(3,4,5-trimethoxyphenyl)propan-1-one 
• 902119-99-7 di(isopropyl)carbamic acid 3-(3,4,5-trimethoxyphenyl)propyl ester 

Downstream Products

• 38838-26-5 N-acetylcolchinol 

Relevant academic research and scientific papers

Synthesis of (S)-(-)-N-acetylcolchinol using intramolecular biaryl oxidative coupling

An asymmetric synthesis of the tubulin polymerisation inhibitor (S)-(-)-N-acetylcolchinol is reported based on an intramolecular biaryl oxidative coupling of a 1,3-diarylpropyl acetamide intermediate using phenyliodonium bis(trifluoroacetate) as the final

Asymmetric synthesis of propargylamides via 3,3′-disubstituted binaphthol-modified alkynylboronates

(Chemical Equation Presented) Alkynylboronates derived from 3,3′-disubstituted-2,2′-binaphthols react with various N-acylimines to give the expected chiral propargylamides with up to 99% ee. This new methodology was applied to the first enantioselective s