83892-07-3

Upstream product

• 94580-89-9 N-benzyloxycarbonyl-L-leucine 2,4,6-trichlorophenyl ester 
• 83892-00-6 N-benzyloxycarbonyl-L-leucine dimethylamide 
• 1161-13-3 N-Cbz-L-Phe 
• 77167-46-5 L-leucine dimethylamide 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 233684-36-1 C₂₂H₃₅N₃O₄ 
• 83892-03-9 N-benzyloxycarbonyl-L-phenylalanyl-L-leucine dimethylamide 

Downstream Products

• 233684-37-2 C₂₇H₄₂N₄O₅ 
• 233684-38-3 C₂₂H₃₄N₄O₃ 
• 233684-39-4 C₂₆H₄₁N₅O₄ 
• 83891-94-5 L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-leucine dimethylamide 
• 83892-11-9 N-benzyloxycarbonyl-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-leucine dimethylamide 

Relevant academic research and scientific papers

A novel chiral pentamine ligand for enantioselective α-alkylation of acyclic lithium amide enolates. Optimization of chiral ligands for asymmetric reactions using solid-phase organic synthesis

(equation presented) A novel pentamine ligand has been developed for enantioselective α-alkylation of simple acyclic lithium amide enolates. It has been demonstrated that solid-phase organic synthesis provides a powerful and rapid method for finding effic

OPIOID-LIKE PEPTIDES. PART I. HYDRAZIDE AND SOME AMIDES OF 2-Leu-ENKEPHALIN

Synthesis and pharmacological properties of hydrazide, methylamide, 2-aminoethylamide, dimethylamide and butylamide of 2-Leu-enkephalin are described.