615268-35-4

Upstream product

• 35466-83-2 allyl methyl carbonate 
• 68-12-2 N,N-dimethyl-formamide 
• 615268-33-2 ethyl 2,2-dibenzyl-pent-4-enoate 
• 615268-34-3 2,2-dibenzyl-pent-4-en-1-ol 

Downstream Products

• 615268-38-7 4-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-3,3-dibenzyl-butanal 
• 615268-37-6 5-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-4,4-dibenzyl-pent-1-ene 
• 904325-38-8 N-benzyl-2,2-dibenzyl-5-methyl-5-nitro-4-oxo-hexylamine 
• 615268-39-8 N-benzyl-N-(tert-butyloxycarbonyl)-2,2-dibenzyl-4-hydroxy-5-methyl-5-nitro-hexylamine 
• 615268-42-3 (4R)-N-benzyl-N-(tert-butyloxycarbonyl)-2,2-dibenzyl-4-diphenylphosphatoxy-5-methyl-5-nitrohexylamine 
• 615268-26-3 (4R)-N-benzyl-2,2-dibenzyl-4-diphenylphosphatoxy-5-methyl-5-nitrohexylamine 
• 615268-41-2 (4R)-N-benzyl-N-(tert-butyloxycarbonyl)-2,2-dibenzyl-4-hydroxy-5-methyl-5-nitrohexylamine 
• 615268-36-5 5-benzylamino-4,4-dibenzyl-pent-1-ene 

Relevant academic research and scientific papers

Difunctionalization of ketones: Via gem -bis(boronates) to synthesize quaternary carbon with high selectivity

All-carbon quaternary centres are significant and prevalent structural frameworks but their preparation routes are rare and challenging, especially methods with common substrates. Herein, we report a convenient process to construct all-carbon quaternary c

Enantioselective alkene radical cations reactions

The reaction of enantiomerically enriched 2-methyl-2-nitro-3-(diphenylphosphatoxy)alkyl radicals with tributyltin hydride and AIBN in benzene at reflux results in the formation of alkene radical cation/anion pairs, which are trapped intramolecularly by am

Enantioselective cyclization of alkene radical cations

(Matrix Presented) Enantiomerically enriched β-(diphenylphosphatoxy) nitroalkanes undergo radical ionic fragmentation, induced by tributyltin hydride and AIBN in benzene at reflux, to give alkene radical cations in contact radical ion pairs. These contact