94001-91-9

Upstream product

• 85-55-2 2-(4-toluoyl)benzoic acid 
• 21615-75-8 3-(4-tolyl)-isobenzofuranone 
• 104-81-4 4-Methylbenzyl bromide 
• 90-02-8 salicylaldehyde 
• 85825-85-0 2-(4-methyl-benzyloxy)-benzaldehyde 
• 690969-91-6 C₁₅H₁₆O₂ 

Downstream Products

• 118343-43-4 α-(2-bromomethylphenyl)-4-methylphenylmethyl bromide 

Relevant academic research and scientific papers

Neighboring lithium-assisted [1,2]-wittig rearrangement: Practical access to diarylmethanol-based 1,4-diols and optically active binol derivatives with axial and sp3-central chirality

A facile and practical methodology for the synthesis of synthetically useful diarylmethanol-based 1,4-diols and enantiomerically pure BINOL-derived diols with axial and sp3-central chirality has been developed through neighboring lithium-promot

4,5 Dihydroimidazole compounds which have useful pharmaceutical utility

A compound of formula (I): STR1 or a pharmaceutically acceptable salt, ester or amide thereof, or a pharmaceutically acceptable solvate thereof, wherein: Z represents a residue of a substituted or unsubstituted aryl group, A1 represents a subst

Reactions of Trialkylborane. VI. Reduction of Carbonyl Compounds with Trialkylborane

The reduction of anhydrides, lactones, esters, carboxylic acids and acyl chlorides with trialkylborane is described.Cyclic anhydrides were reduced with 4 mol eq of trialkylborane at temperatures above 300 deg C to give diol derivatives via the lactones.Lactones, esters, carboxylic acids and acyl chlorides were reduced under similar conditions to give the corresponding alcohol derivatives.Keywords-reduction; trialkylborane; anhydride; lactone; ester; carboxylic acid; alcohol; carbonyl compound