117471-55-3

Upstream product

• 117471-53-1 (Z)-1,4-bis(p-methoxybenzyl)-3-(4'-hydroxy-2'-butenoxy)-2,5-piperazinedione 
• 117471-51-9 N-(p-methoxybenzyl)-2-acetamide 
• 117471-50-8 N,N'-bis(p-methoxybenzyl)-α-aminoacetamide 
• 117471-54-2 (Z)-1,4-bis(p-methoxybenzyl)-3-(4'-chloro-2'-butenoxy)-2,5-piperazinedione 

Downstream Products

• 135365-97-8 6,8-bis(p-methoxybenzyl)-6,8-diaza-1-hydroxy-2-ethenylbicyclo<2.2.2>octane-5,7-dione 
• 135365-95-6 (Z)-9,11-bis(p-methoxybenzyl)-9,11-diaza-7-hydroxy-2-oxabicyclo<5.2.2>undec-4-ene-8,10-dione 
• 135365-94-5 (Z)-9,11-bis(p-methoxybenzyl)-9,11-diaza-7-methyl-2-oxabicyclo<5.2.2>undec-4-ene-8,10-dione 
• 135365-99-0 6,8-bis(p-methoxybenzyl)-6,8-diaza-1-hydroxy-4-methyl-2-ethenylbicyclo<32.1>octane-5,7-dione 
• 135365-98-9 6,8-bis(p-methoxybenzyl)-6,8-diaza-1-hydroxy-4-methyl-2-ethenyl-bicyclo<2.2.2>octane-5,7-dione 
• 135393-45-2 6,8-bis(p-methoxybenzyl)-6,8-diaza-1-dihydroxy-2-ethenylbicyclo<2.2.2>octane-5,7-dione 
• 135366-02-8 6,8-bis(p-methoxybenzyl)-6,8-diaza-4-<(tert-butyldimethylsilyl)oxy>-3-(hydroxymethyl)bicyclo<2.2.2>octane-5,7-dione 
• 135366-01-7 6,8-bis(p-methoxybenzyl)-6,8-diaza-4-<(tert-butyldimethylsilyl)oxy>-2-ethenyl-1-hydroxybicyclo<3.2.1>octane-5,7-dione 
• 135366-00-6 6,8-bis(p-methoxybenzyl)-6,8-diaza-4-<(tert-butyldimethylsilyl)oxy>-2-ethenyl-1-hydroxybicyclo<2.2.2>octane-5,7-dione 
• 135365-96-7 (Z)-9,11-bis(p-methoxybenzyl)-9,11-diaza-7-<(tert-butyldimethylsilyl)oxy>-2-oxabicyclo<5.2.2>undec-4-ene-8,10-dione 
• 135366-03-9 6,8-bis(p-methoxybenzyl)-6,8-diaza-<(tert-butyldimethylsilyl)oxy>-3-<(phenylselenyl)methyl>bicyclo<2.2.2>octane-5,7-dione 

Relevant academic research and scientific papers

Novel ring contractions via [2,3] wittig type rearrangements: Synthesis of 2-desoxy-2-methylenebicyclomycin

Bridgehead carbanion generation of bicyclo[5.2.2] and bicyclo[7.2.2] allyl ether bridged piperazinediones result in novel ring contractions via unusual [2,3] Wittig type and [3,3] Claisen rearrangements. The application of the [2,3] Wittig rearrangements

Versatile New Approach to the Synthesis of Monosubstituted and Bicyclic Piperazine-2,5-diones: Unusual in Situ Generation and Enolate Addition to a Cumulene

Dichloroacetyl chloride condenses with glycinamide 9 to furnish the versatile precursor 10, which cyclizes to the mono (ether) substituted piperazinediones 11 upon treatment with alkoxides.A new intramolecular enolate C-C bond-forming cyclization from the