117751-78-7

Upstream product

• 4434-61-1 N-(benzyloxycarbonyl)methionine 
• 501-53-1 benzyl chloroformate 
• 1152-62-1 Cbz-Met-OH 
• 75266-39-6 methyl (S)-2-<<(benzyloxy)carbonyl>amino>-4-(methylsulfinyl)butanoate 
• 75266-40-9 N-benzyloxycarbonyl-L-α-vinylglycine methyl ester 
• 83972-33-2 N-<(benzyloxy)carbonyl>-DL-methionine methyl ester 
• 80656-34-4 N-<(benzoyloxy)carbonyl>-D,L-vinylglycine methyl ester 
• 56762-93-7 methyl (S)-2-(benzyloxycarbonylamino)-4-methylmercaptobutanoate 

Downstream Products

• 98777-31-2 (S)-2-Benzyloxycarbonylamino-3-hydroxy-4-phenylsulfanyl-butyric acid methyl ester 
• 1219595-82-0 C₁₉H₂₈N₂O₇ 
• 1219595-84-2 C₂₃H₂₈N₂O₇ 
• 1219595-98-8 C₂₃H₂₈N₂O₇ 
• 1219595-87-5 C₂₃H₃₄N₂O₉ 
• 1219595-99-9 C₂₃H₂₈N₂O₈ 
• 98777-62-9 methyl DL-2-<(benzyloxy)carbonylamino>-4-chloro-3-hydroxybutanoate 
• 117751-72-1 methyl (2S,3R)-3-acetoxy-2-(benzyloxycarbonyl)aminobutanoate 
• 117751-88-9 O-acetyl-N-benzyloxycarbonyl-L-allothreonine methyl ester 
• 129956-64-5 (S)-2-Benzyloxycarbonylamino-4-(4-chloro-phenylamino)-3-hydroxy-butyric acid methyl ester 
• 117751-71-0 2(S),3(R)-methyl 2-N-benzyloxycarbonylamino-4-bromo-3-hydroxybutanoate 
• 117751-87-8 (2S,3R)-2-Benzyloxycarbonylamino-4-bromo-3-hydroxy-butyric acid methyl ester 
• 98777-35-6 2-Oxo-3,6-dihydro-2H-[1,3]oxazine-4-carboxylic acid methyl ester 
• 129956-63-4 (Z)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-but-2-enoic acid methyl ester 

Relevant academic research and scientific papers

Structure and Stereochemistry of Three Phytotoxins, Syringomycin, Syringotoxin and Syringostatin, Produced by Pseudomonas syringae pv. syringae

The structures of two phytotoxins, syringomycin and syringotoxin, produced by Pseudomonas syringae pv. syringae, were determined.Several amino acid residues of syringomycin were different from those in the syringostatins.Syringotoxin B proved to be syringostatin A.The three kinds of phytotoxins showed close structural similarity, and the stereochemistry of their components was deduced and compared.

UNUSUAL α-AMINOACIDS FROM VINYLGLYCINE

The easily available L-vinylglycine derivative 1 is used in the synthesis of unusual multifunctional α-aminoacids such as 2 and 3.