95675-61-9

Upstream product

• 32945-67-8 Boc-Leu₃-OBzl 
• 71145-33-0 H-Leu₂-OBzl 
• 32925-57-8 Boc-Leu-Leu-OBzl 
• 125814-33-7 N-(tert-butoxycarbonyl)-L-leucine N-carboxyanhydride 
• 1738-77-8 L-leucine benzyl ester p-toluenesulfonate 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 

Downstream Products

• 75666-41-0 Boc-Ala₂-Leu₃-OBzl 
• 75666-42-1 Boc-Pro₂-Leu₃-OBzl 
• 75666-40-9 H-Leu₃-OBzl 
• 75666-45-4 Boc-Ala₂-Leu₃-Pro₂-Leu₃-OBzl 
• 75666-43-2 H-Pro₂-Leu₃-OBzl*HCl 
• 92782-19-9 Boc-Leu₆-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

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

Design of the Synthetic Route for Helical Peptides. Synthesis and Solubility of Model Peptides Having a Helical Structure

Fragment condensations between amino- and carboxyl-components of hydrophobic decapeptides, which have a β-sheet structure in the solid state and are insoluble in DMF, NMP, and DMSO, were examined in a mixture of CH2Cl2 and TFE (4/1, v/v) using various cou

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