423157-99-7

Upstream product

• 253599-39-2 (+)-(3R,4S)-3-benzyloxy-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1-(2-propenyl)-2-azetidinone 
• 253599-40-5 (+)-cis-1-allyl-3-(R)-benzyloxy-4-(S)-[1-(S),2-dihydroxyethyl]-azetidin-2-one 
• 19810-31-2 Benzyloxyacetyl chloride 
• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 253599-41-6 (+)-(3R,4R)-3-benzyloxy-1-(2-propenyl)-4-oxoazetidine-2-carbaldehyde 

Downstream Products

• 423158-06-9 1-[(1S,2S,5R)-2-((R)-1-Benzyloxy-2-hydroxy-ethyl)-7-methyl-6-oxa-3,7-diaza-bicyclo[3.2.1]oct-3-yl]-propenone 
• 1053697-44-1 (R)-((1S,2S,5R)-3-Acryloyl-7-methyl-6-oxa-3,7-diaza-bicyclo[3.2.1]oct-2-yl)-benzyloxy-acetaldehyde 
• 423158-02-5 (R)-2-Benzyloxy-2-((1S,2S,5R)-7-methyl-6-oxa-3,7-diaza-bicyclo[3.2.1]oct-2-yl)-ethanol 

Relevant academic research and scientific papers

Diastereoselective route to novel fused or bridged tricyclic β-lactams through intramolecular nitrone-alkene cycloaddition of 2-azetidinone-tethered alkenylaldehydes - Synthetic applications to carbacephams and cyclic β-amino acid derivatives

A convenient, regio- and stereoselective direct route to optically pure unusually fused or bridged tricyclic β-lactams has been developed by use of intramolecular nitrone-alkene cycloaddition (INAC) reactions of easily available monocyclic 2-azetidinone-t