82081-93-4

Upstream product

• 15761-38-3 L-N-Boc-Ala 
• 1738-78-9 L-phenylalanine benzyl ester p-toluene-sulfonic acid salt 
• 962-39-0 L-Phenylalanine benzyl ester 
• 2462-32-0 L-phenylalanine benzyl ester hydrochloride 

Downstream Products

• 161431-25-0 Boc-Pro-Gly-Arg(Tos)-Ala-Phe-OBzl 
• 2448-58-0 (S)-2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)-3-phenylpropanoic acid 
• 1382351-61-2 Boc-L-Ala-L-Phe-D-Val-OMe 
• 947189-48-2 Boc-D-Hpg-D-Orn(SES)-D-aThr-L-Hpg-D-Hpg-L-Ala-L-Phe-OBn 
• 947189-47-1 Boc-L-Hpg-D-Hpg-L-Ala-L-Phe-OBn 

Relevant academic research and scientific papers

Backbone-Enabled Directional Peptide Macrocyclization through Late-Stage Palladium-Catalyzed δ-C(sp2)?H Olefination

C?H activation methods for peptide macrocyclization have the potential to provide peptidomimetics and cyclic peptides with expanded structural diversity. Now, a highly versatile peptide macrocyclization strategy via late-stage palladium-catalyzed δ-C(sps

METHOD FOR PRODUCING CARBOXYLIC ACID AMIDE COMPOUND, AND CATALYST AND FLOW PRODUCTION SYSTEM

PROBLEM TO BE SOLVED: To provide a new production method that allows a dehydration condensation reaction between carboxylic acid and amine, and a catalyst. SOLUTION: A method for producing a carboxylic acid amide compound includes the step for causing a r

The greening of peptide synthesis

The synthesis of peptides by amide bond formation between suitably protected amino acids is a fundamental part of the drug discovery process. However, the required coupling and deprotection reactions are routinely carried out in dichloromethane and DMF, b

Alanine scan of [L-Dap2]ramoplanin A2 aglycon: Assessment of the importance of each residue

In efforts that define the importance of each residue and that identify key regions of the molecule, an alanine scan of the ramoplanin A2 aglycon, a potent antibiotic that inhibits bacterial cell wall biosynthesis, is detailed. As a consequence of both it

Synthesis of immunoaduvant conjugates with HIV-derived peptide inducing peptide-specific antibody

MDP and lipopeptide analog conjugates inducing HIV-derived peptide-specific antibody without adding further macromolecular carriers or adjuvants were synthesized.