110351-27-4

Upstream product

• 67-56-1 methanol 
• 10323-40-7 2-bromoisovaleric acid 
• 20194-18-7 sodium phenyl-methanolate 
• 4026-18-0 2-hydroxy-3-methylbutanoic acid 
• 17417-00-4 methyl 2-hydroxy-3-methylbutanoate 
• 100-39-0 benzyl bromide 

Downstream Products

• 56972-71-5 2-benzyloxy-3-methylbutanoic acid 
• 149287-51-4 (4R*)-Methyl 2-(N-benzoylamino)-4-(benzyloxy)-5-methyl-(2Z)-hexenoate 
• 149287-52-5 (4R*)-Methyl 2-(N-benzoylamino)-4-(benzyloxy)-5-methyl-(2E)-hexenoate 
• 149287-49-0 (4R*)-Methyl 4-(benzyloxy)-2--5-methyl-(2Z)-hexenoate 
• 149287-50-3 (4R*)-Methyl 4-(benzyloxy)-2--5-methyl-(2E)-hexenoate 
• 96925-01-8 2-(Benzyloxy)-3-methylbutanal 
• 84994-63-8 2-Benzyloxy-3-methyl-butan-1-ol 
• 110298-78-7 methyl (S)-2-(benzyloxy)-3-methylbutanoate 
• 90211-83-9 methyl (R)-2-benzyloxy-3-methylbutanoate 

Relevant academic research and scientific papers

Stereoselective Bromination of Dehydroamino Acids with Controllable Retention or Inversion of Olefin Configuration

Dehydroamino acids react with brominating reagents to produce syn-α-bromo imines as the major products, which undergo tautomerization to mixtures of the diastereomeric (E)- and (Z)-β-bromo-α,β-dehydroamino acids upon treatment with base.Herein, we examine

ENZYME-MEDIATED ASYMMETRIC HYDROLYSIS OF α-BENZYLOXYCARBOXYLIC ESTERS

Incubation of dl-α-benzyloxycarboxylic esters with grown cells of a bacterium, Corynebacterium equi IFO 3730, afforded the chiral esters of high optical purities via asymmetric hydrolysis.This reaction has been revealed to have a wide applicability to alkene- and arylalkene-carboxylic esters.