838864-66-7

Upstream product

• 1453202-89-5 (3S,4S,5R)-4-(benzyloxy)-5-((R)-1-iodotetradecyl) tetrahydrofuran-3-ylcarbamate 
• 1453202-88-4 tert-butyl (2S,3R)-3-(benzyloxy)-1-hydroxyoctadec-4-en-2-ylcarbamate 
• 1453202-86-2 (S)-tert-butyl 4-((R)-1-(benzyloxy)hexadec-2-enyl)-2, 2-dimethyloxazolidine-3-carboxylate 
• 838864-62-3 (4S,6R)-4-(1-benzyloxyallyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 114301-34-7 tert-butyl (S)-4-((R)-1-hydroxyallyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 102308-32-7 (4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Stereoselective total synthesis of Jaspine B (Pachastrissamine) utilizing iodocyclization and an investigation of its cytotoxic activity

The stereoselective synthesis of Jaspine B has been achieved from easily available (S)-Garner's aldehyde. The trisubstituted tetrahydrofuran core of Jaspine B was constructed by utilizing a diastereoselective iodocyclization as the key step. Deiodination

The first synthesis of the anhydrophytosphingosine pachastrissamine (jaspine B) from Garner's aldehyde

The synthesis of the natural anhydrophytosphingosine pachastrissamine (jaspine B) 1a from Garner's aldehyde is described.