184432-11-9

Upstream product

• 347-54-6 5-fluoro-2-hydroxybenzaldehyde 
• 1521-51-3 rac-3-bromocyclohexene 

Downstream Products

• 187225-99-6 (2aS,5aR,10bS,10cR)-9-Fluoro-1-((R)-1-phenyl-ethyl)-1,2a,3,4,5,5a,10b,10c-octahydro-2,6-dioxa-1-aza-aceanthrylene 
• 187226-00-2 (2aR,5aS,10bR,10cS)-9-Fluoro-1-((R)-1-phenyl-ethyl)-1,2a,3,4,5,5a,10b,10c-octahydro-2,6-dioxa-1-aza-aceanthrylene 
• 187226-02-4 (2aR,5aS,10bS,10cS)-9-Fluoro-1-((R)-1-phenyl-ethyl)-1,2a,3,4,5,5a,10b,10c-octahydro-2,6-dioxa-1-aza-aceanthrylene 
• 187226-01-3 (2aS,5aR,10bR,10cR)-9-Fluoro-1-((R)-1-phenyl-ethyl)-1,2a,3,4,5,5a,10b,10c-octahydro-2,6-dioxa-1-aza-aceanthrylene 

Relevant academic research and scientific papers

A new protocol for the conversion of isoxazolidines to 1,3-amino alcohols

A number of fused-ring isoxazolidines 3 have been successfully transformed into the corresponding 1,3-amino alcohols 5 through oxidation with 3-chloroperbenzoic acid and subsequent catalytic hydrogenation.