250291-84-0

Upstream product

• 124994-66-7 (S)-benzyl-4-oxo-2-<<(1,1-dimethylethoxy)carbonyl>amino>butanoate 
• 35059-50-8 t-butyl diazoacetate 
• 75-65-0 tert-butyl alcohol 
• 844644-72-0 2-tert-butoxycarbonylamino-4-(2,2-dimethyl-4,6-dioxo-[1,3]dioxan-5-ylidene)-4-hydroxy-butyric acid benzyl ester 

Downstream Products

• 682743-10-8 (2'S,1''S)-2-[2'-tert-butoxycarbonylamino-2'-(1''-methoxycarbonyl-2''-phenyl-ethylcarbamoyl)-ethyl]-6-methyl-1-oxido-4-phenyl-pyridine-3,5-dicarboxylic acid di-tert-butyl ester 
• 682742-80-9 (2'S)-2-(2'-benzyloxycarbonyl-2'-tert-butoxycarbonylamino-ethyl)-6-methyl-1-oxido-4-phenyl-pyridine-3,5-dicarboxylic acid di-tert-butyl ester 
• 682742-78-5 (2'S)-2-(2'-benzyloxycarbonyl-2'-tert-butoxycarbonylamino-ethyl)-6-methyl-4-phenyl-pyridine-3,5-dicarboxylic acid di-tert-butyl ester 
• 682742-90-1 (2'S)-2-(2'-tert-butoxycarbonylamino-2'-carboxy-ethyl)-6-methyl-1-oxido-4-phenyl-pyridine-3,5-dicarboxylic acid di-tert-butyl ester 
• 596828-20-5 (2'S)-2-(2'-tert-butoxycarbonylamino-2'-carboxyethyl)-6-methyl-4-phenylpyridine-3,5-dicarboxylic acid di-tert-butyl ester 
• 682742-85-4 (2'S)-2-(2'-amino-2'-benzyloxycarbonyl-ethyl)-6-methyl-1-oxido-4-phenyl-pyridine-3,5-dicarboxylic acid di-tert-butyl ester 
• 682742-84-3 (2'S)-2-(2'-amino-2'-benzyloxycarbonyl-ethyl)-6-methyl-4-phenyl-pyridine-3,5-dicarboxylic acid di-tert-butyl ester 

Relevant academic research and scientific papers

Multicomponent Hantzsch cyclocondensation as a route to highly functionalized 2- and 4-dihydropyridylalanines, 2- and 4-pyridylalanines, and their N-oxides: Preparation via a polymer-assisted solution-phase approach

An improved and efficient entry to highly functionalized β-(2-pyridyl)- and β-(4-pyridyl)alanines and the corresponding 1,4-dihydro and N-oxide derivatives has been developed by one-pot thermal Hantzsch-type cyclocondensation of aldehyde-ketoester-enamine

A new scaffold for the stereoselective synthesis of α-O-linked glycopeptide mimetics

α-O-Linked glycohomoglutamates are obtained as diastereomerically pure compounds by chemo-, regio-, and stereoselective cycloadditions between glycals and aspartic acid derivatives. The latter constitute orthogonally functionalized scaffolds for glycopept