133995-30-9

Upstream product

• 625388-36-5 (2S,4S)-4-tritylthio-1-(allyloxycarbonyl)pyrrolidine-2-carboxylic acid methyl ester 
• 76-83-5 trityl chloride 
• 136140-32-4 (3S,5S)-3-acetylthio-1-allyloxycarbonyl-5-(hydroxymethyl)pyrrolidine 
• 126408-14-8 methyl (2S,4R)-N-(allyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylate 
• 3695-77-0 triphenylmethanethiol 
• 126438-17-3 (2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxy-2-methoxycarbonylpyrrolidine 

Downstream Products

• 147505-95-1 (2S,4S)-2-Formyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-14-8 (2S,4S)-2-aminomethyl-4-tritylthio-1-(allyloxycarbonyl)pyrrolidine 
• 909395-13-7 (2S,4S)-2-azidomethyl-4-tritylthio-1-(allyloxycarbonyl)pyrrolidine 
• 909395-15-9 (2S,4S)-2-isothiocyanatomethyl-4-tritylthio-1-(allyloxycarbonyl)pyrrolidine 
• 909395-41-1 (2S,4S)-2-{[(Pyrrolidine-1-carbonyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-36-4 (2S,4S)-2-{[(Pyrrolidine-1-carbothioyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-16-0 (2S,4S)-2-{[(Thiomorpholine-4-carbothioyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-30-8 (2S,4S)-2-{[(Morpholine-4-carbothioyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-39-7 (2S,4S)-2-{[(Morpholine-4-carbonyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-17-1 (2S,4S)-2-{[(Thiomorpholine-4-carbonyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-34-2 (2S,4S)-2-{[(Piperazine-1-carbothioyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-38-6 (2S,4S)-2-{[(2-Hydroxymethyl-pyrrolidine-1-carbothioyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-32-0 (2S,4S)-2-{[(4-Hydroxy-piperidine-1-carbothioyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 909395-40-0 (2S,4S)-2-{[(4-Hydroxy-piperidine-1-carbonyl)-amino]-methyl}-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 

Relevant academic research and scientific papers

Novel lβ-methylcarbapenems having cyclic sulfonamide moieties: Synthesis and evaluation of in vitro antibacterial activity

The synthesis of a new series of 1β-methylcarbapenems having cyclic sulfonamide moieties is described. Their in vitro antibacterial activities against both Gram-positive and Gram-negative bacteria were tested and the effect of substituent on the pyrrolidi

Synthesis and?biological evaluation of?1β-methylcarbapenems having cyclic thiourea moieties and?their?related compounds

The synthesis of a new series of 1β-methylcarbapenems having cyclic thiourea moieties is described. Their in vitro antibacterial activities against both Gram-positive and Gram-negative bacteria were tested and the effect of substituent on the pyrrolidine

Synthesis and Antibacterial Activity of 1β-Methyl-2-(5-substituted oxadiazolo pyrrolidin-3-yl-thio)carbapenem Derivatives

Synthesis of a new series of 1β-methylcarbapenems with a substituted oxadiazolopyrrolidine moiety is described. Their in vitro antibacterial activities against both Gram-positive and Gram-negative bacteria were tested and the effect of the substituent on

Synthesis and antibacterial activity of 1β-methyl-2-[5-(N-substituted-2-hydroxy iminoethyl)pyrrolidin-3-ylthio]carbapenem derivatives

The synthesis of a new series of 1-methylcarbapenems having the substituted thiazolopyrrolidine moiety is described. Their in vitro antibacterial activities against both gram-positive and gram-negative bacteria were tested and the effect of substituent on

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

2-(2-vinylpyrrolidinylthio)carbapenem derivatives

A compound of the formula: STR1 wherein R1 is a hydrogen atom or a methyl group, R2 is a hydrogen atom or a lower alkyl group, each of R3, R4 and R5 is a hydrogen atom or a lower alkyl group, or Rsup