410527-41-2

Upstream product

• 160309-18-2 (1R,4R,5S,6R)-4,5-(isopropylidenedioxy)-7-(4'-methylphenylsulfonyl)-7-azabicyclo<4.1.0>hept-2-ene 
• 163082-04-0 (1R,4S,5S,6R)-3-bromo-4,5-(isopropylidenedioxy)-7-(4'-methylphenylsulfonyl)-7-azabicyclo<4.1.0>hept-2-ene 
• 410527-38-7 (1S,2R,3S,4R,4aS,11bR)-4-benzylamino-1-(tert-butyloxycarbonyloxy)-2,3-(isopropylidenedioxy)-2,3,4,4a,6,11b-hexahydro-1H-5,8,10-trioxa-cyclopenta[b]phenanthrene-6-one 
• 410527-10-5 N-benzyl-N-[(1R,2R,3S,4S,5S,6S)-2-(benzo[1,3]dioxolo-5-ylmethoxy)-4,5-(isopropylidenedioxy)-7-oxabicyclo[4.1.0]hept-3-yl]-4-'-methylbenzenesulfonamide 
• 410527-31-0 (1S,2R,3S,4R,4aS,11bR)-1-hydroxy-2,3-(isopropylidenedioxy)-6-(2'-methoxyethoxy)-4-[N-benzyl-(4'-methylphenylsulfonyl)amino]-2,3,4,4a,6,11b-hexahydro-1H-5,8,10-trioxa-cyclopenta[b]phenanthrene 
• 410527-34-3 (1S,2R,3S,4R,4aS,11bR)-4-benzylamino-1-(tert-butyloxycarbonyloxy)-2,3-(isopropylidenedioxy)-6-(2'-methoxyethoxy)-2,3,4,4a,6,11b-hexahydro-1H-5,8,10-trioxa-cyclopenta[b]phenanthrene 
• 410527-27-4 (1S,2R,3S,4R,4aS,11bR)-1-hydroxy-2,3-(isopropylidenedioxy)-4-[N-benzyl-(4'-methylphenylsulfonyl)amino]-2,3,4,4a,6,11b-hexahydro-1H-5,8,10-trioxa-cyclopenta[b]phenanthrene 
• 393165-22-5 (2S,4R,5S,6S)-5,6-(isopropylidenedioxy)-3-(4'-methylphenylsulfonyl)-8-oxa-3-azatricyclo[5.1.0.0]octane 
• 130669-75-9 (3aS,7aS)-4-bromo-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 67451-62-1 cis-(1S,2S)-1,2-dihydroxy-3-bromocyclohexa-3,5-diene 

Downstream Products

• 410527-45-6 (1S,2R,3S,4R,4aS,11bR)-2-benzylamino-1,3,4-trihydroxy-1,2,3,4,4a,11b-hexahydro-1H-5,8,10-trioxa-cyclopenta[b]phenanthrene-6-one 
• 410527-48-9 (1S,2R,3S,4R,4aS,11bR)-2-benzylamino-1,3,4-tri(acetoxy)-1,2,3,4,4a,11b-hexahydro-1H-5,8,10-trioxa-cyclopenta[b]phenanthrene-6-one 

Relevant academic research and scientific papers

Structure assignment of aminoconduritols by 15N NMR correlation spectroscopy; synthesis of a positional isomer of 7-deoxypancratistatin

A positional isomer of 7-deoxypancratistatin was synthesized in 12 steps from epoxyaziridines 4 and 5. An intermolecular opening of the aziridine rather than the epoxide in the early stages of the synthesis led to 13, which did not match the properties of