73252-35-4

Upstream product

• 62574-13-4 L-cystine tert-butyl ester 
• 98-88-4 benzoyl chloride 
• 62574-13-4 (2S,2'S)-di-tert-butyl 3,3'-disulfanediylbis(2-aminopropanoate) 
• 73284-29-4 N-benzoyl-D-cystine di-tert-butyl ester 
• 73284-29-4 (R)-2-Benzoylamino-3-((R)-2-benzoylamino-2-tert-butoxycarbonyl-ethyldisulfanyl)-propionic acid tert-butyl ester 

Downstream Products

• 73252-38-7 C₁₄H₁₈ClNO₃S 
• 73252-38-7 C₁₄H₁₈ClNO₃S 
• 73252-40-1 (2R,3S,5S)-3-((S)-2-Benzoylamino-2-tert-butoxycarbonyl-ethylsulfanyl)-2-chloro-5-methoxymethoxy-hexanoic acid methyl ester 
• 85880-01-9 (2R,3S,5S)-2-((S)-2-Benzoylamino-2-tert-butoxycarbonyl-ethylsulfanyl)-3-chloro-5-methoxymethoxy-hexanoic acid methyl ester 
• 73252-41-2 (E)-(S)-2-((S)-2-Benzoylamino-2-tert-butoxycarbonyl-ethylsulfanyl)-5-methoxymethoxy-hex-2-enoic acid methyl ester 
• 73252-42-3 (Z)-(S)-2-((S)-2-Benzoylamino-2-tert-butoxycarbonyl-ethylsulfanyl)-5-methoxymethoxy-hex-2-enoic acid methyl ester 
• 73252-44-5 (Z)-(S)-2-((S)-2-Benzoylamino-2-carboxy-ethylsulfanyl)-5-hydroxy-hex-2-enoic acid methyl ester 
• 73285-67-3 (Z)-(3S,9R)-3-Benzoylamino-9-methyl-2-oxo-3,4,8,9-tetrahydro-2H-[1,5]oxathionine-6-carboxylic acid methyl ester 
• 73252-45-6 (R)-5-((R)-2-Benzoylamino-propionyloxy)-hexanoic acid methyl ester 
• 288318-39-8 tert-butyl (2S)-2-(benzoylamino)-3-{[(4S)-1-(ethoxycarbonyl)-2-hydroxy-4-(methoxymethoxy)pentyl]thio}propanoate 
• 288318-40-1 (2S)-2-(benzoylamino)-3-{[(Z,4S)-1-(ethoxycarbonyl)-4-hydroxypent-1-enyl]thio}propanoic acid 
• 288318-38-7 tert-butyl (2S)-2-benzoylamino-3-{[(1-ethoxycarbonyl)methyl]thio}propanoate 
• 73252-40-1 (2R,3S)-3-((R)-2-Benzoylamino-2-tert-butoxycarbonyl-ethylsulfanyl)-2-chloro-5-methoxymethoxy-hexanoic acid methyl ester 
• 73252-39-8 (2R,3S)-2-((R)-2-Benzoylamino-2-tert-butoxycarbonyl-ethylsulfanyl)-3-chloro-5-methoxymethoxy-hexanoic acid methyl ester 

Relevant academic research and scientific papers

A novel route to the vinyl sulfide nine-membered macrocycle moiety of griseoviridin

The synthetic potentialities of cerium(III) chloride are demonstrated by the synthesis of a nine-membered ring heterocycle component of Griseoviridin (3) in optically active form. The key step involves the stereospecific formation of the α-carbalkoxy alke