81254-79-7

Upstream product

• 632-20-2 D-Threonine 
• 81254-81-1 3-(2-benzyloxybenzoyl)-1,3-thiazolidine-2-thione 
• 81254-80-0 (2R,3S)-methyl 2-(2-(benzyloxy)benzamido)-3-hydroxybutanoate 
• 100-39-0 benzyl bromide 
• 55142-16-0 methyl 2-(benzyloxy)benzoate 
• 14389-86-7 2-benzyloxybenzoic acid 
• 119-36-8 methyl salicylate 

Downstream Products

• 89965-53-7 (4R,5R)-2-(2-hydroxyphenyl)-4-methoxycarbonyl-5-methyl-4,5-dihydro-oxazole 
• 89965-55-9 (4S,5R)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 74149-70-5 parabactin 
• 89965-57-1 (4S,5R)-N-<3-(benzyloxycarbonylamino)propyl>-N-<4-(benzyloxycarbonylamino)butyl>-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-oxazole-4-carboxamide 
• 89965-52-6 N-(2-hydroxybenzoyl)-D-threonine methyl ester 
• 89965-54-8 (4S,5R)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-oxazole-4-carboxylic acid 
• 81254-80-0 (2R,3S)-methyl 2-(2-(benzyloxy)benzamido)-3-hydroxybutanoate 

Relevant academic research and scientific papers

LANTHANIDE CLUSTERS AND METHODS OF USE THEREOF

The present invention is directed to multinuclear lanthanides chiral clusters, based on phenyl-oxazoline-amide (POxA) ligands, and to methods of use thereof. The chiral clusters of this invention are highly fluorescent with high stability.

Total Synthesis of Parabactin, a Spermidine Siderophore

The stereoselective total synthesis of parabactin (1) has been efficiently carried out using substituted 1,3-thiazolidine-2-thione as a leaving group.