89965-54-8

Upstream product

• 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 
• 89965-52-6 N-(2-hydroxybenzoyl)-D-threonine methyl ester 
• 434953-01-2 C₂₅H₂₃NO₄ 
• 119-36-8 methyl salicylate 
• 81254-80-0 (2R,3S)-methyl 2-(2-(benzyloxy)benzamido)-3-hydroxybutanoate 
• 81254-79-7 (2R,3S)-2-(2-(benzyloxy)benzamido)-3-hydroxybutanoic acid 
• 81254-81-1 3-(2-benzyloxybenzoyl)-1,3-thiazolidine-2-thione 
• 55142-16-0 methyl 2-(benzyloxy)benzoate 
• 14389-86-7 2-benzyloxybenzoic acid 
• 69-72-7 salicylic acid 

Downstream Products

• 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 
• 89965-55-9 (4S,5R)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Total Synthesis of the Proposed Structure of Mycobactin J

The total synthesis of the proposed structure of mycobactin J (MJ), a metabolite of Mycobacterium tuberculosis, is presented. The highlights of the synthesis include a careful control of the Z-stereochemistry of the unsaturated long chain fatty acid, a biomimetic construction of the oxazoline building block and the carriage of an unprotected phenol throughout the synthesis.

A latent oxazoline electrophile for N-O-C bond formation in pseudomonine biosynthesis

Nitrogen-heteroatom bonds figure prominently in the structural, chemical, and functional diversity of natural products. In the case of Pseudomonas siderophore pseudomonine, an N-O hydroxamate linkage is found uncommonly configured in an isoxazolidinone ri

Dehydrative cyclization catalyzed by the combination of molybdenum(VI) oxides and benzoic acids: First synthesis of the antitumour substance BE-70016

The dehydrative cyclization of N-(o-hydroxybenzoyl)threonine derivative la is efficiently promoted by the combined use of molybdenum(VI) oxides and benzoic acids bearing electron-with-drawing substituents. In the presence of ammonium molybdate [(NH4

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.