150309-57-2

Upstream product

• 150309-71-0 (2R,4S)-4-acetylthio-2-[3-(N-methyl-N-p-nitrobenzyloxycarbonylamino)propyl]-N-p-nitrobenzyloxycarbonylpyrrolidine 
• 189188-38-3 4-nitrobenzyl (4R,5S,6S)-3-[(diphenylphosphono)oxy]-6-[(R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate 
• 93711-81-0 (4-nitrophenyl)methyl (4R,5R,6S)-3-[(diphenoxyphosphinyl)oxy]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate 
• 1026985-13-6 (2R,4S)-4-Mercapto-2-{3-[methyl-(4-nitro-benzyloxycarbonyl)-amino]-propyl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester 

Relevant academic research and scientific papers

1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 2. Synthesis and antibacterial activity of 5-aminopropyl and 5-aminopropenyl pyrrolidine derivatives

The synthesis and biological activity of (1R,5S,6S)-2-[(3S,5S)-5-substituted pyrrolidin-3-ylthio]-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3 -carboxylic acid, in which aminopropyl, aminopropenyl, and aminopropynyl groups were introduced as substitu

Alkylaminoalkylpyrrolidinylthiocarbapenem derivatives

A compound of the formula: STR1 wherein R1 is a hydrogen atom or a methyl group, R2 is a hydrogen atom or a negative charge, X is a group of --N(R3)R4 (wherein R3 is a lower alkyl group, and R4/