709658-73-1

Upstream product

• 107-11-9 1-amino-2-propene 

Downstream Products

• 709658-76-4 1,1-dimethylethyl (2R,3R,4S)-2-[(1S)-5-[(4-methoxyphenyl)methoxy]-1-(phenylmethoxy)pentyl]-3,4-bis(phenylmethoxy)-1-pyrrolidinecarboxylate 
• 709658-78-6 (1'S,2R,3R,4S)-1',3,4-tris(phenylmethoxy)-2-pyrrolidinepentanol 
• 709658-79-7 (1R,2S,9S,9aR)-octahydro-1,2,9-tris(phenylmethoxy)-1H-pyrrolo[1,2-a]azepine 
• 709658-75-3 1,1-dimethylethyl (2R,3R,4S)-2-[(1S)-1-hydroxy-5-[(4-methoxyphenyl)methoxy]pentyl]-3,4-dihydroxy-1-pyrrolidinecarboxylate 
• 709658-74-2 1,1-dimethylethyl (2S)-2,5-dihydro-2-[(1S)-1-hydroxy-5-[(4-methoxyphenyl)methoxy]pentyl]-1H-pyrrole-1-carboxylate 
• 709658-71-9 1,1-dimethylethyl N-[(1S,2S)-1-ethenyl-2-hydroxy-6-[(4-methoxyphenyl)methoxy]hexyl]-N-(2-propenyl)carbamate 

Relevant academic research and scientific papers

Synthesis of (+)-(1R,2S,9S,9aR)-octahydro-1H-pyrrolo[1,2-a]azepine-1,2,9- triol: A potential glycosidase inhibitor

The title compound was prepared as a potential glycosidase inhibitor. Key steps in the synthesis are vinyl epoxide aminolysis, ring-closing metathesis, cis-dihydroxylation and then ring closure.