121195-33-3

Upstream product

• 101979-88-8 2-carboxy-2-deoxy-β-D-arabino-pentopyranosylaminolactam 
• 101979-87-7 2-carboxy-2-deoxy-3,4-di-O-(trimethylsilyl)-β-D-arabinopyranosylaminolactam 
• 100-44-7 benzyl chloride 

Downstream Products

• 113437-34-6 N-benzyl-2-carboxy-2-deoxy-α-D-arabinopentopyranosylaminolactam 
• 113474-30-9 N-benzyl-2-carboxy-2-deoxy-2-hydroxymethyl-β-D-threotetrofuranosylaminolactam 
• 113437-39-1 N-benzyl-2-carboxy-2-deoxy-2-hydroxymethyl-α-L-erythrotetrofuranosylaminolactam 
• 113474-29-6 (3R, 4R) N-benzyl-3-hydroxymethyl-4-(hydroxyethoxy)-azetidinone-2 
• 113437-37-9 (3S, 4R) N-benzyl-3-hydroxymethyl-4-(hydroxyethoxy)-azetidinone-2 
• 113437-36-8 (3R,4R)-1-Benzyl-2-oxo-4-(2-oxo-ethoxy)-azetidine-3-carbaldehyde 

Relevant academic research and scientific papers

STEREOCONTROLLED ENTRY TO 1-OXAPENAMS AND 1-OXACEPHEMS FROM CARBOHYDRATES

N-Benzyl-2-carboxy-2-deoxypento and hexopyranosylaminolactams readily available via addition of trichloroacetyl isocyanate to substituted glycals, were transformed into enantiomerically pure N-benzyl-4-alkoxy-3-hydroxymethylazetidinones-2.The transformati

OPTICALLY PURE 3,4-DISUBSTITUED AZETIDINONES FROM SUGARS

Glycolic cleavage of the vic-diol grouping present in N-benzyl-2-carboxy-2-deoxypento and hexopyranosylaminolactams (5, 6, and 7) with sodium metaperiodate under standard conditions leads to formation of reactive dialdehydes 13 and 14 which upon standing