66876-64-0

Upstream product

• 101221-79-8 ^tBOC-(S)-Phe-ΔPhe-Gly-OMe 
• 42267-16-3 (d,l)-phenylserine ethyl ester hydrochloride 
• 110694-57-0 Boc-Phe-(β-OH)Phe-OH 
• 110697-93-3 Boc-Phe-Phe-azlactone 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 50903-54-3 N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine pentafluorophenyl ester 
• 7625-57-2 methyl 2-((2S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)acetate 
• 105224-79-1 H-Phe-Gly-OMe*TFA 
• 7625-59-4 L-phenylalanylglycine methyl ester hydrochloride 
• 4192-12-5 dicyclohexylammonium N-(tert-butoxycarbonyl)-L-phenylalaninate 

Downstream Products

• 82816-76-0 N-tert-butoxycarbonyl-L-phenylalanine-L-phenylalanine-glycine 
• 66876-65-1 H-Phe-Phe-Gly-OMe*HCl 
• 1025882-52-3 Boc-Phe-Phe-Gly-Phe-Phe-Gly-OMe 
• 101301-86-4 cyclo-(-Gln-Phe-Phe-Gly-Leu-Met-) 
• 101301-88-6 H-Gln-Phe-Phe-Gly-OMe*HCl 
• 101301-84-2 Boc-Leu-Met-Gln-Phe-Phe-Gly-OMe 
• 101301-85-3 Boc-Leu-Met-Gln-Phe-Phe-Gly-NH-NH₂ 
• 101301-92-2 H-Leu-Met-Gln-Phe-Phe-Gly-NH-NH₂*HCl 
• 101301-81-9 Boc-Gln-Phe-Phe-Gly-OMe 
• 51165-05-0 H-Phe-Phe-Gly-Leu-Met-NH₂ 
• 61123-13-5 pyroglutamyl-phenylalanyl-phenylalanine-glycyl-leucyl-methionine amide 
• 73148-99-9 N-t-Boc-Phe-Phe-Gly-Leu-Met-NH₂ 
• 82155-83-7 6-Amino-hexanoic acid {(S)-1-[(S)-1-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-phenyl-ethyl}-amide 
• 71890-54-5 (S)-4-Methyl-2-{2-[(S)-3-phenyl-2-((S)-3-phenyl-2-phenylacetylamino-propionylamino)-propionylamino]-acetylamino}-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide 

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

Isolation, structure and synthesis of mahafacyclin B, a cyclic heptapeptide from the latex of Jatropha mahafalensis

The isolation, structure and synthesis of mahafacyclin B, a cyclic heptapeptide from the latex of Jatropha mahafalensis was discussed. The structure was elucidated by chemical degradation, tendem mass spectrometry, homo- and heteronuclear NMR experiments

Peptide Conformations, 41.- A Unique Conformation of the Cyclic Pentapeptide cyclo(-Pro-Pro-Phe-Phe-Gly-) in DMSO

The title compound 1 was obtained on two different ways by cyclization between Gly5 and Pro1 as well as between Phe4 and Gly5.Investigations by 1H-, 13C-, and 15N-NMR spectroscopy show that one single conformati

SYNTHESIS OF CHIRAL OLIGOPEPTIDES BY MEANS OF CATALYTIC ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDES

Asymmetric hydrogenation of Ac-ΔTyr(Ac)-(S)-Ala-Gly-OMe (6), Ac-ΔTyr(Ac)-(R)-Ala-Gly-(S)-Phe-OMe (7), Ac-ΔPhe-NH-CH(R)-CH2-OCH2Ph (10), HCO-ΔPhe-(S)-Leu-OMe (16), X-AA-ΔPhe-AA'-OMe ( 5: X=tBOC, CBZ, CF3CO; AA, AA'= α-amino acid ), and t