150884-60-9

Upstream product

• 15082-42-5 lithium benzyloxide 

Downstream Products

• 150884-61-0 (R,S)-3-benzyloxy-4-hydroxy-Δ²-isoxazoline butyrate 
• 150884-64-3 (R)-3-benzyloxy-4-amino-Δ²-isoxazoline 
• 150884-65-4 (S)-3-benzyloxy-4-amino-Δ²-isoxazoline 
• 151004-13-6 (R)-3-Benzyloxy-4,5-dihydro-isoxazol-4-ol 
• 151004-14-7 (S)-3-Benzyloxy-4,5-dihydro-isoxazol-4-ol 
• 150884-67-6 (S)-3-benzyloxy-4-acetylamino-Δ²-isoxazoline 
• 150884-66-5 (R)-3-benzyloxy-4-acetylamino-Δ²-isoxazoline 
• 150884-62-1 (R)-3-benzyloxy-4-azido-Δ²-isoxazoline 
• 150884-63-2 (S)-3-benzyloxy-4-azido-Δ²-isoxazoline 
• 151004-15-8 (S)-3-benzyloxy-4-hydroxy-Δ²-isoxazoline butyrate 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of acetyl (R)-(+)- and (S)-(-)-cycloserine

The two enantiomers of acetyl cycloserine 8, the immediate precursors of the chiral forms of cycloserine 1, were prepared in enantiomeric excess higher than 98% by means of lipase-catalyzed hydrolysis of 3-benzyloxy-4-hydroxy-Δ2-isoxazoline but