24182-13-6

Upstream product

• 400019-81-0 C₃₁H₄₄N₂O₇Si 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 52813-63-5 (5R)-2,3,4,5-tetrahydro-5-hydroxymethyl-2-furanone 
• 108-24-7 acetic anhydride 
• 128075-94-5 (R)-5-{[(tert-butyldiphenylsilyl)oxy]methyl}dihydrofuran-2(3H)-one 
• 400019-88-7 C₁₆H₂₈N₂O₉S 
• 400019-83-2 (3S,5R)-5-Hydroxy-tetrahydro-pyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester 
• 400019-87-6 C₁₅H₂₆N₂O₇ 
• 262363-89-3 (3S,5R)-5-Hydroxy-tetrahydro-pyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester 3-methyl ester 
• 400019-84-3 (3S,5S)-5-Acetoxy-1-(2,4-dinitro-phenyl)-hexahydro-pyridazine-3-carboxylic acid methyl ester 
• 214354-12-8 (3S,5S)-5-Acetoxy-tetrahydro-pyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester 3-methyl ester 

Relevant academic research and scientific papers

Convenient synthesis of (3S,5S)-5-hydroxy- and (3R,5S)-5-chloropiperazic acids of a peptide antibiotic, monamycin G3

Convenient synthesis of (3S,5S)-5-hydroxy- and (3R,5S)-5-chloropiperazic acids, which are the important constituting moieties of an antibiotic monamycin G3, and their possible stereoisomers constructing of similar antibiotics was achieved from