540508-52-9

Upstream product

• 540508-28-9 (2R,3R)-3-{4-[2-((2S,3S)-2-Benzyloxycarbonylamino-3-methyl-pentanoylamino)-1-triisopropylsilanyloxy-ethyl]-phenoxy}-2-(tert-butyl-dimethyl-silanyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 128836-20-4 tert-butyl (2R,3R)-2-[(tert-butyldimethylsiloxy)methyl]-3-hydroxypyrrolidine-1-carboxylate 
• 123278-55-7 (4R,5S)-5-<(1,1-dimethylethyl)dimethylsilyl>oxymethyl-4-hydroxy-1-<(1,1-dimethylethoxy)carbonyl>-pyrrolidin-2-one 
• 540508-45-0 2-(tert-butyl-dimethyl-silanyloxymethyl)-3-(4-formyl-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 540508-30-3 2-(tert-butyl-dimethyl-silanyloxymethyl)-3-(4-cyano-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 540508-47-2 2-(tert-butyl-dimethyl-silanyloxymethyl)-3-[4-(1-hydroxy-2-nitro-ethyl)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 540508-65-4 2-(tert-butyl-dimethyl-silanyloxymethyl)-3-[4-(2-nitro-1-triisopropylsilanyloxy-ethyl)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 540508-49-4 3-[4-(2-amino-1-triisopropylsilanyloxy-ethyl)-phenoxy]-2-(tert-butyl-dimethyl-silanyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 

Downstream Products

• 540508-57-4 (2S,3R)-3-{4-[2-((2S,3S)-2-Amino-3-methyl-pentanoylamino)-1-triisopropylsilanyloxy-ethyl]-phenoxy}-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 
• 543689-94-7 (3R,7S,10S)-10-((S)-sec-Butyl)-8,11-dioxo-14-phenylselanyl-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-triene-6-carboxylic acid tert-butyl ester 
• 540508-53-0 (2S,3R)-3-{4-[2-((2S,3S)-2-Benzyloxycarbonylamino-3-methyl-pentanoylamino)-1-triisopropylsilanyloxy-ethyl]-phenoxy}-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 

Relevant academic research and scientific papers

Studies toward a synthesis of C3-epimauritine D: Construction of the macrocycle

We successfully synthesized a 14-membered cyclic enamide of C3-epimauritine D from the cis-2,3-pyrrolidinediol derivative. Treatment of the pyrrolidinediol with nitrobenzonitrile in an SNAr reaction efficiently installed the desired aryl-alkyl ether linkage on the N-heterocyclic system. Macrocyclization was successfully achieved by the use of TFFH as the peptide coupling reagent in the presence of HOAt.