607358-20-3

Upstream product

• 27914-73-4 4-acetoxybenzoyl chloride 
• 137686-07-8 2-{[(tert-butoxy)carbonyl]amino}-3-ethoxy-3-oxopropanoic acid 
• 102831-44-7 diethyl tert-butoxycarbonylaminomalonate 

Downstream Products

• 607358-42-9 2-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester 
• 607358-40-7 2-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester 
• 607358-36-1 (2S,3S)-2-tert-Butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-propionic acid 
• 607358-38-3 (2R,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-propionic acid ethyl ester 
• 607358-50-9 (2-{4-hydroxy-phenyl}-2-oxo-ethyl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis of proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway

(Matrix presented) A chemoenzymatic synthesis was described to prepare proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway. The successful synthesis of these fragile molecules relies heavily on mild enz