334832-30-3

Upstream product

• 334832-27-8 C₆₄H₈₈N₈O₁₅Si₂ 
• 334832-28-9 C₆₄H₈₆N₈O₁₄Si₂ 
• 334832-29-0 C₅₈H₇₂N₈O₁₄Si 
• 334832-17-6 (4S,5R)-4-((Z)-1-{4-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((S)-1-methoxycarbonyl-2-methyl-propylcarbamoyl)-ethylcarbamoyl]-5-methyl-oxazol-2-yl}-propenylcarbamoyl)-2,2,5-trimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 334832-25-6 (S)-2-{[2-((S)-1-Benzyloxycarbonylamino-2-triethylsilanyloxy-ethyl)-5-methyl-oxazole-4-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-propionic acid methyl ester 
• 334832-19-8 2-{N-Cbz-N,O-isopropylidene-L-Thr-[(Z)-1-amino-1-propenyl]}-5-methyloxazole-4-carbonyl-L-Ser-L-Val-OH 
• 334832-18-7 2-{N-Cbz-N,O-isopropylidene-L-Thr-[(Z)-1-amino-1-propenyl]}-5-methyloxazole-4-carbonyl-L-Ser-L-Val-OMe 
• 334832-23-4 (S)-4-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methoxycarbonyl-ethylcarbamoyl]-5,2',2'-trimethyl-4',5'-dihydro-[2,4']bioxazolyl-3'-carboxylic acid benzyl ester 
• 334832-26-7 (S)-2-{[2-((S)-1-Amino-2-triethylsilanyloxy-ethyl)-5-methyl-oxazole-4-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-propionic acid methyl ester 
• 334832-24-5 (S)-2-{[2-((S)-1-Benzyloxycarbonylamino-2-hydroxy-ethyl)-5-methyl-oxazole-4-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-propionic acid methyl ester 
• 334832-15-4 Cbz-Ser(TBS)-L-Val-OMe 
• 334832-20-1 (S)-4-((1S,2R)-2-Hydroxy-1-methoxycarbonyl-propylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 334832-22-3 (S)-5,2',2'-Trimethyl-4',5'-dihydro-[2,4']bioxazolyl-4,3'-dicarboxylic acid 3'-benzyl ester 
• 334832-21-2 (S)-5,2',2'-Trimethyl-4',5'-dihydro-[2,4']bioxazolyl-4,3'-dicarboxylic acid 3'-benzyl ester 4-methyl ester 

Downstream Products

• 334832-31-4 4-(1-{4-[1-(1-{1-[4-(2-hydroxy-1-methoxycarbonyl-ethylcarbamoyl)-5-methyl-oxazol-2-yl]-vinylcarbamoyl}-2-methyl-propylcarbamoyl)-vinylcarbamoyl]-5-methyl-oxazol-2-yl}-propenylcarbamoyl)-2,2,5-trimethyl-oxazolidine-3-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Useful synthesis of the main dehydrohexapeptide segment of a macrocyclic antibiotic, berninamycin B

The useful synthesis of tetradehydrohexapeptide segment 2, which is the main skeleton of a macrocyclic antibiotic, berninamycin B, was first achieved. The skeleton 2 is constructed, in turn, of 2-[(Z)-1-amino-1-propenyl]-5-methyl-oxazole-4-carboxylic acid, α-dehydroalanine (ΔAla), L-Val, 2-[1-amino-1-ethenyl]-5-methyloxazole-4-carboxylic acid residues, besides L-Thr and ΔAla at the N- and C-termini, respectively.