95477-51-3

Upstream product

• 53937-02-3 4-(benzyloxy)pyridin-2(1H)-one 
• 77149-75-8 (1R,4R)-5-Benzyloxy-2-aza-bicyclo[2.2.0]hex-5-en-3-one 
• 77149-75-8 5-benzyloxy-2-azabicyclo<2.2.0>hex-5-en-3-one 

Downstream Products

• 136737-99-0 (1S,4S,5R)-5-Benzyloxy-3-oxo-2-aza-bicyclo[2.2.0]hexane-2-carboxylic acid (2-chloro-acetyl)-amide 
• 136738-00-6 (1R,2S,4R)-2-Benzyloxy-4-ureido-cyclobutanecarboxylic acid methyl ester 
• 136738-00-6 (1R,2R,4S)-2-Benzyloxy-4-ureido-cyclobutanecarboxylic acid methyl ester 
• 136738-01-7 ((1R,2S,3S)-3-Benzyloxy-2-hydroxymethyl-cyclobutyl)-urea 
• 136738-01-7 ((1R,2R,3S)-3-Benzyloxy-2-hydroxymethyl-cyclobutyl)-urea 

Relevant academic research and scientific papers

Cycloadditions in Syntheses. Part 27. rel-(1R,4R,5S)-5-Hydroxy-2-azabicyclohexan-3-one and its Derivatives: Synthesis and Transformation to Azetidin-2-ones

The title compound, a synthetic equivalent of 4-(2-oxoethyl)azetidin-2-one, has been synthesized as a stable crystalline compound from the 2-pyridone having an appropriately protected 4-hydroxy group via photopyridine formation, catalytic hydrogenation, a

rel-(1R,4R,5S)-5-HYDROXY-3-OXO-2-AZABICYCLOHEXANE, A STABLE SYNTHETIC EQUIVALENT OF 4-(2-OXOETHYL)AZETIDIN-2-ONE

The title compound, a synthetic equivalent of 4-(2-oxoethyl)-azetidin-2-one, has been synthesized as a stable crystalline solid either from 4-(t-butyldimethylsilyloxy)- or 4-benzyloxy-2-pyridone via photopyridone formation, catalytic hydrogenation, and de