1365993-63-0

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 18261-30-8 (E,E)-methyl heptan-2,5-dieneoate 
• 1365993-55-0 methyl (S,E)-3-(N-allylamino)hept-5-enoate 
• 1365993-61-8 (2R,4S,5R,Z)-1-tert-butoxycarbonyl-2-(6-benzyloxyhex-2-enyl)-4,5-epoxypiperidine 
• 1365993-60-7 (2S,4S,5R)-1-tert-butoxycarbonyl-2-(2-oxoethyl)-4,5-epoxypiperidine 
• 1365993-59-4 (S,S,S)-2-[1-tert-butoxycarbonyl-4-hydroxy-5-iodopiperidin-2-yl]ethanal 
• 1365993-58-3 (S,S,S)-N⁽⁶⁾-tert-butoxycarbonyl-8-iodo-2-oxa-6-azabicyclo[3.3.1]nonan-3-one 
• 1365993-54-9 methyl (S,S,E)-3-[n-allyl-N-(α-methyl-p-methoxybenzyl)amino]hept-5-enoate 
• 1365993-57-2 (S)-2-[1-tert-butoxycarbonyl-1,2,3,6-tetrahydropyridin-2-yl]ethanoic acid 
• 1365993-56-1 methyl (S,E)-3-[N-allyl-N-(tert-butoxycarbonyl)amino]hept-5-enoate 

Downstream Products

• 1365993-64-1 (2R,4S,5R)-1-tert-butoxycarbonyl-2-(6-[1-phenyl-1H-tetrazol-5-ylsulfonyl]hexyl)-4,5-epoxypiperidine 

Relevant academic research and scientific papers

Polysubstituted piperidines via iodolactonization: Application to the asymmetric synthesis of (+)-pseudodistomin D

Conjugate addition of lithium (S)-N-allyl-N-(α-methyl-p- methoxybenzyl)amide to methyl (E,E)-hepta-2,5-dienoate furnished the corresponding β-amino ester. N-Protecting group manipulation, ring-closing metathesis, and ester hydrolysis gave enantiopure [N(1