603959-05-3

Upstream product

• 70-11-1 α-bromoacetophenone 
• 603959-03-1 (4R,5S)-[5-(benzylaminomethyl)-2,2-dimethyl[1,3]dioxolan-4-yl]methanol 
• 100-46-9 benzylamine 
• 189996-60-9 2,3-O-isopropylidene-D-erythrose 

Downstream Products

• 603959-24-6 (1S,5S,7R)-3-(9-fluorenylmethoxycarbonyl)-5-phenyl-7-endo-hydroxymethyl-6,8-dioxa-3-azabicyclo[3.2.1]octane 
• 603959-08-6 (1S,5S,7R)-3-tert-butoxycarbonyl-5-phenyl-7-endo-hydroxymethyl-6,8-dioxa-3-azabicyclo[3.2.1]octane 
• 603959-07-5 (1S,5S,7R)-5-phenyl-7-endo-hydroxymethyl-6,8-dioxa-3-azabicyclo[3.2.1]octane 
• 603959-06-4 (1S,5S,7R)-3-benzyl-5-phenyl-7-endo-hydroxymethyl-6,8-dioxa-3-azabicyclo[3.2.1]octane 

Relevant academic research and scientific papers

Enantiospecific synthesis of 3-aza-6,8-dioxa-bicyclo[3.2.1]octane carboxylic acids from erythrose

New methodology for the synthesis of enantiopure 3-aza-6,8-dioxa-bicyclo[3.2.1]octane-carboxylic acids belonging to 7-endo-BTAa sub-class of γ/δ amino acids is described. The novelty is the use of 2,3-O-isopropylidene-erythrose instead of meso-tartaric ac