92125-62-7

Upstream product

• 92216-27-8 1,4-dimethyl-3-(2'-thiopyridyl)-6-(2-γ-butyrolactonyl)-2,5-piperazinedione (anti, major diastereomer) 
• 92098-11-8 1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-(2-γ-butyrolactonyl)-2,5-piperazinedione (syn, major diastereomer) 
• 92216-26-7 1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-(2-γ-butyrolactonyl)-2,5-piperazinedione (syn, minor diastereomer) 
• 92098-03-8 syn-1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-<1''-(hydroxymethyl)-3''-(hydroxypropyl)>-2,5-piperazinedione (major diastereomer) 
• 92216-29-0 anti-1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-<1''-(hydroxymethyl)-3''-(hydroxypropyl)>-2,5-piperazinedione (major diastereomer) 
• 95782-44-8 syn-1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-<1''-(hydroxymethyl)-3''-(hydroxypropyl)>-2,5-piperazinedione (minor diastereomer) 
• 95782-38-0 8,10-bis(p-methoxybenzyl)-8,10-diaza-5-<(methylsulfonyl)methyl>-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 95782-41-5 8,10-bis(p-methoxybenzyl)-8,10-diaza-5-<(methylsulfonyl)methyl>-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 95782-43-7 8,10-bis(p-methoxybenzyl)-8,10-diaza-5-<(phenylselenyl)methyl>-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 92098-14-1 8,10-bis(p-methoxybenzyl)-8,10-diaza-5-<(phenylselenyl)methyl>-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 92098-12-9 8,10-bis(p-methoxybenzyl)-8,10-diaza-5-(hydroxymethyl)-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 95782-35-7 1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-<1''-<((methylsulfonyl)oxy)methyl>-3''-<((tert-butyldimethylsilyl)oxy)propyl>>-2,5-piperazinedione 
• 95694-62-5 1,4-bis(p-methoxybenzyl)-3-(2'-thiopyridyl)-6-<1''-(hydroxymethyl)-3''-<((tert-butyldimethylsilyl)oxy)propyl>>-2,5-piperazinedione 
• 92098-16-3 8,10-bis(p-methoxybenzyl)-8,10-diaza-5-methylene-6-hydroxy-2-oxabicyclo<4.2.2>decane-7,9-dione 

Downstream Products

• 38129-37-2 (+/-)-bicyclomycin 

Relevant academic research and scientific papers

Stereocontrolled Total Synthesis of (+/-)- and (+)-Bicyclomycin

The completely regio- and stereocontrolled total synthesis of bicyclomycin (1) is described in 12 chemical steps.A new carbon-carbon bond-forming reaction on 1,4-dibenzyl- and 1,4-bis(p-methoxybenzyl)-3,6-bis(2'-thiopyridyl)-2,5-piperazinediones (10 and 4