117834-24-9

Upstream product

• 16373-02-7 2,4-di-tert-butyl-6-hydroxymethylphenol 
• 122-04-3 4-nitro-benzoyl chloride 
• 96-76-4 2,4-di-tert-Butylphenol 

Downstream Products

• 117834-26-1 2,4-Di-tert-butyl-6-{[((1S,2R)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amino]-methyl}-phenol 
• 117834-25-0 2,4-tert-dibutyl-6-(((S)-2-(hydroxymethyl)pyrrolidin-1-yl)methyl)phenol 
• 117834-23-8 2,4-Di-tert-butyl-6-{[((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amino]-methyl}-phenol 

Relevant academic research and scientific papers

ZINC COMPLEXES OF CHIRAL PHENOLS AS CATALYSTS FOR ENANTIOSELECTIVE ADDITION OF ORGANOZINC REAGENTS TO ALDEHYDES

A class of zinc(II) chelates with chiral tertiary amino phenolic alcohols serve as effective catalysts for the enantioselective addition of diethylzinc to aromatic aldehydes with predictable absolute stereochemistry.

Asymmetric synthesis XXII: Asymmetric catalytic trimethylsilylcyanation of benzaldehyde by novel Ti(IV)-chiral Schiff base complexes

Benzaldehyde has been trimethylsilylcyanated with a catalyst prepared in situ from titanium tetraisopropoxide and a novel chiral Schiff base. Both (R) and (S) cyanohydrins are obtained in moderate e.e. values.