360776-32-5

Upstream product

• 360776-31-4 (1S,2S)-2-((S)-2-Hydroxy-1-phenyl-ethylamino)-cyclohept-4-enol 
• 360776-11-0 (2S,4S)-2-Pent-4-enoyl-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 360776-14-3 (2S,4S)-2-((S)-1-Hydroxy-pent-4-enyl)-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 360776-17-6 (3S,6S,6aS)-6-But-3-enyl-3-phenyl-tetrahydro-1,5-dioxa-3a-aza-pentalen-4-one 

Relevant academic research and scientific papers

Ring-closing metathesis of diolefinic oxazolidinones: A new access to tropanes and aminocyclitols

Ring-closing metathesis of diolefinic oxazolidinones prepared through N-Boc-2-acyl or α,β-epoxy oxazolidine methodology give stereodefined bicyclic oxazolidinones. The 5,6-membered bicyclic oxazolidinones are then converted into new aminocyclitols by diastereoselective dihydroxylation whereas their 5,7-membered bicyclic homologues are transformed into tropanic alkaloids through an aminocyclization step.