205647-76-3

Upstream product

• 205647-74-1 (R)-tert-butyl 2,2-dimethyl-4-[(tosyloxy)methyl]-oxazolidine-3-carboxylate 
• 110774-06-6 L-N-(benzyloxycarbonyl)-3-[3-hydroxy-4-(benzyloxy)phenyl]-N-methylalanine methyl ester 
• 205647-75-2 (S)-4-{2-Benzyloxy-5-[(S)-2-(benzyloxycarbonyl-methyl-amino)-2-methoxycarbonyl-ethyl]-phenoxymethyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Downstream Products

• 205647-79-6 (S)-3-{4-Benzyloxy-3-[(S)-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-(tert-butyl-diphenyl-silanyloxy)-propoxy]-phenyl}-2-(benzyloxycarbonyl-methyl-amino)-propionic acid pentafluorophenyl ester 
• 205647-78-5 (S)-3-{4-Benzyloxy-3-[(S)-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-(tert-butyl-diphenyl-silanyloxy)-propoxy]-phenyl}-2-(benzyloxycarbonyl-methyl-amino)-propionic acid 
• 205647-77-4 (S)-3-{4-Benzyloxy-3-[(R)-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-hydroxy-propoxy]-phenyl}-2-(benzyloxycarbonyl-methyl-amino)-propionic acid methyl ester 

Relevant academic research and scientific papers

Synthetic study of ustiloxin analogs: Benzylic oxidation of 13-membered cyclic peptide by lead tetraacetate

The 13-membered cyclic peptides (5,6), analogs of phomopsin-ustiloxin class of antibiotics, have been synthesized. Benzylic hydroxyl group was introduced in desired stereochemistry by lead tetraacetate oxidation followed by methanolysis.