736933-75-8

Upstream product

• 25245-34-5 1-bromo-2,5-dimethoxybenzene 
• 736933-40-7 (2S)-2-benzhydryloxy-1-(2,5-dimethoxy-phenyl)-hept-4-en-1-one 
• 736933-15-6 2-(benzhydryloxy)-1-(2,5-dimethoxyphenyl)-ethanone 
• 7348-71-2 (E)-1-bromo-2-pentene 

Downstream Products

• 736933-73-6 (1S)-benzoic acid 1-(2,5-dimethoxy-benzoyl)-hex-3-enyl ester 

Relevant academic research and scientific papers

Asymmetric phase-transfer catalyzed glycolate alkylation, investigation of the scope, and application to the synthesis of (-)-ragaglitazar

Asymmetric glycolate alkylation using a protected acetophenone surrogate under solid-liquid phase-transfer conditions is a new approach to the synthesis of 2-hydroxy esters and acids. Diphenylmethyloxy-2,5-dimethoxyacetophenone 1 with a trifluorobenzyl ci

Phase-transfer-catalyzed asymmetric glycolate alkylation

Asymmetric surrogate glycolate alkylation has been performed under phase-transfer conditions. Diphenylmethyloxy-2,5-dimethoxyacetophenone with trifluorobenzyl cinchonidinium catalyst and cesium hydroxide provided alkylation products at -35°C in high yield