2471-53-6

Upstream product

• 19542-54-2 N-benzyloxycarbonyl-L-valyl-L-valine 
• 6306-52-1 L-valine methylester hydrochloride 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 1999-88-8 methyl (S)-2-((S)-2-benzyloxycarbonyl-amino-3-methylbutyrylamino)-3-methylbutyrate 
• 4070-48-8 L-Valine methyl ester 
• 21761-30-8 L-valyl-L-valine methyl ester 

Relevant academic research and scientific papers

Copper-catalyzed enantioselective conjugate addition of dialkylzinc reagents to enones with new peptidyl phosphane ligands

Copper catalysts based on new peptidyl phosphane ligands have been developed for enantioselective conjugate additions of dialkylzinc reagents to cyclic enones. Enantioselectivities greater than 97% ee have been observed.

Reaction of [(Cp2TiCH3)(THF)+] [BPh4-] with tripeptide derivatives: Formation of cationic (peptide)titanocene complexes

A series of Z- and Boc-protected tripeptide methyl esters [Z-/Boc-5 to -12(pept)] was prepared using the amino acids glycine, alanine and valine. In both the alanine and the valine series a single glycine unit was introduced and its position inside the tr