114646-30-9

Usage

InChI:InChI=1/C24H34N4O6/c1-14(2)11-16(27-23(33)34-24(3,4)5)21(31)26-17-13-19(29)28(22(17)32)18(20(25)30)12-15-9-7-6-8-10-15/h6-10,14,16-18H,11-13H2,1-5H3,(H2,25,30)(H,26,31)(H,27,33)/t16-,17-,18?/m0/s1

Upstream product

• 3392-09-4 Boc-Leu-ONSu 
• 73537-90-3 H-Asu-Phe-NH₂*HBr 
• 139033-28-6 Z-D-Asp-Phe-NH₂ 
• 139033-45-7 Z-D-Asp(OBzl)-OPfp 
• 5241-70-3 Z-D-Asp(OBzl)-Phe-NH₂ 
• 73537-63-0 Z-D-Asu-Phe-NH₂ 
• 50903-50-9 N-[(1,1-dimethylethoxy)carbonyl]-L-leucine pentafluorophenyl ester 
• 3479-47-8 Z-Asp(OBzl)-OH 
• 17543-13-4 pentafluorophenyl ester of benzyloxycarbonyl-β-benzylaspartic acid 
• 139033-32-2 Boc-Leu-Asp(Phe-NH₂)-OBzl 
• 97530-02-4 (tert-butyloxycarbonyl)-L-leucyl-β-benzyl-L-aspartyl-L-phenylalanine amide 
• 73537-63-0 Z-Asu-Phe-NH₂ 
• 129095-55-2 Z-D-Asp(OBu^t)-Phe-NH₂ 
• 5241-62-3 (benzyloxycarbonyl)-β-benzyl-D-aspartic acid 

Downstream Products

• 129095-59-6 Boc-Leu-D-Asn-Phe-NH₂ 
• 129095-58-5 Boc-Leu-Asn-Phe-NH₂ 
• 129095-60-9 Boc-Leu-D-iAsn-Phe-NH₂ 
• 129095-60-9 Boc-Leu-iAsn-Phe-NH₂ 

Relevant academic research and scientific papers

Aspartate Racemization in Synthetic Peptides. Part 2. Tendency to Racemization of Aminosuccinyl Residue

Aminosuccinyl (Asu) peptides, containing a strained ring system, are very vulnerable to epimerization and, during their formation, even as transients, in the presence of nucleophilic and nonnucleophilic bases, partial epimerization occurs.In the presence

AMMONOLYSIS MEDIATED SIDE REACTIONS OF β-TERT-BUTYL ASPARTYL PEPTIDES

Ammonolysis of Z-Asp(OBut)-Phe-NH2 and Boc-Leu-Asp(OBut)-Phe-NH2, as well as their diastereisomers, resulted not only in transpeptidated, but also in epimerized peptides through a complex mechanism.Key compounds of these transformati