97512-77-1

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 74805-42-8 N-carboxy-α-dehydrophenylalanine anhydride 

Downstream Products

• 43189-54-4 Boc-L-Phe-L-Leu-L-Ala-OMe 
• 123975-78-0 Boc-D-Phe-L-Leu-L-Ala-OMe 
• 123975-79-1 Boc-D-Phe-L-Ala-L-Leu-OMe 
• 70396-33-7 Boc-L-Phe-L-Ala-L-Leu-OMe 
• 150993-06-9 N-Boc-ΔPhe-L-Ser-OMe 
• 150993-10-5 (S)-2-((Z)-1-tert-Butoxycarbonylamino-2-phenyl-vinyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 119767-98-5 Boc-(Z)-ΔPhe-L-Leu-L-Ala-OMe 
• 119767-97-4 Boc-(Z)-ΔPhe-L-Ala-L-Leu-OMe 

Relevant academic research and scientific papers

Correlation between the Configurational Structure and the Asymmetric Hydrogenation of Δ1-, Δ2-, and Δ3-Dehydrotripeptides

The heterogeneous catalytic hydrogenation of Δ1-dehydrotripeptides (Δ1-DHP), which have a β-turn structure, was carried out to give the corresponding tripeptides indicative of the very large diastereomeric excess, comparing with thos

Dehydrooligopeptides. XIV. Syntheses of 2-[(Z)-1-amino-1-alken-1-yl]oxazole-4-carboxylic acid and the main common skeleton of thiostrepton peptide antibiotics, A10255G and J

The practical synthesis of a unique dehydropentapeptide (2), the common main skeleton of thiostrepton macrocyclic peptide antibiotics, A10255G and J, is described. Peptide 2 is constructed from a novel 2-[(Z)-1-amino-1-propen-1-yl]oxazole-4-carboxylic aci