349642-77-9

Upstream product

• 108-05-4 vinyl acetate 
• 144924-01-6 β-azido-α-(4-methoxyphenyl)ethanol 
• 108-22-5 Isopropenyl acetate 
• 6595-28-4 2-azido-1-(4-methoxyphenyl)ethan-1-one 
• 108-24-7 acetic anhydride 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 

Downstream Products

• 50802-66-9 (S)-N-[2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide 
• 46084-19-9 (S)-(+)-2-amino-1-(4-methoxyphenyl)-1-ethanol 
• 297765-47-0 (S)-(+)-2-azido-1-(4-methoxyphenyl)-1-ethanol 

Relevant academic research and scientific papers

Chemoenzymatic resolution of β-azidophenylethanols by candida antarctica and their application for the synthesis of chiral benzotriazoles

As resoluc?o?es cine?ticas de (±)-β- azidofeniletano?is foram realizadas usando a lipase de Candida antarctica fornecendo os compostos enantiomericamente enriquecidos, (R)-β- azidofeniletano?is e acetato de (S)-β-azidofeniletila em bons excessos enantiome

Non-enzymatic kinetic resolution of 1,2-azidoalcohols using a planar-chiral DMAP derivative catalyst

Optically pure 1,2-azidoalcohols are widely used as precursors for other high value organic products. A non-enzymatic kinetic resolution procedure for the stereoselective synthesis of chiral 1,2-azidoalcohols from the readily available racemic counterpart

Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol

An efficient synthesis of optically active β-azido alcohols from their ketoazides by a one-pot reduction and an in situ lipase resolution protocol is described. The synthetic utility of this procedure has been illustrated by its application in the practic

Stereoselective acylations of 1,2-azidoalcohols with vinyl acetate, catalyzed by lipase Amano PS

Lipase PS-catalyzed kinetic resolution of vicinal azidoalcohols was accomplished. The enzymatic reaction rates and the enantioselectivities were significantly enhanced under the ultrasonic irradiation.