71145-33-0

Upstream product

• 32925-57-8 Boc-Leu-Leu-OBzl 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 1738-77-8 L-leucine benzyl ester p-toluenesulfonate 
• 125814-33-7 N-(tert-butoxycarbonyl)-L-leucine N-carboxyanhydride 
• 2462-35-3 L-leucine benzyl ester hydrochloride 

Downstream Products

• 95675-61-9 H-Leu₃-OBzl*HCl 
• 32945-67-8 Boc-Leu₃-OBzl 

Relevant academic research and scientific papers

Peptide Mechanosynthesis by Direct Coupling of N-Protected α-Amino Acids with Amino Esters

In view of developing alternatives to classical peptide synthesis strategies that suffer from low efficacy and negative environmental impact, the reactivity of N-protected α-amino acids, amino esters, and N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide was

Unambiguous characterization of anisotropic foldamer packing in a foldecture with an elongated hexagonal plate shape

Herein we correlate secondary structure perturbation with changes in the solid-state molecular architectures of an elongated hexagonal plate-shaped foldecture derived from the self-assembly of rigid 12-helical β-peptide foldamers to which a flexible C-ter

Environmentally benign peptide synthesis using liquid-assisted ball-milling: Application to the synthesis of Leu-enkephalin

This paper describes an original methodology for peptide bond synthesis avoiding toxic solvents and reactants. Ball-milling stoichiometric amounts of Boc-protected α-amino acid N-carboxyanhydrides (Boc-AA-NCA) or Boc-protected α-amino acid N-hydroxysuccin

Liquid-Phase Peptide Synthesis by Fragment Condensation on a Soluble Polymer Support. III. The Influence of the Content and the Chain Length of a Peptide Anchored to a Soluble Polymer Support on the Reactivity of the Amino-free Terminal of the Peptide

In order to investigate the influence of the content and the chain length of a peptide anchored to a soluble polymer support on the reactivity of the amino-free terminal of the peptide, chloromethylated polystyrene, which is a starting material for peptid