405224-76-2

Upstream product

• 136175-13-8 trans-1-(tert-Butoxycarbonyl)-2,5-bis(ethoxycarbonyl)pyrrolidine 
• 116724-78-8 O₁-tert-butyl O₂,O₅-diethyl pyrrolidine-1,2,5-tricarboxylate 
• 405224-69-3 C₁₆H₁₉N₃O₄S₂ 
• 866396-75-0 2,5-cis-dicarbamoylpyrrolidine-1-carboxylic acid tert-butyl ester 
• 116724-80-2 (2S,5R)-Pyrrolidine-1,2,5-tricarboxylic acid 1-tert-butyl ester 
• 405224-72-8 2-((4S,5R)-5-Methyl-2-oxo-oxazolidin-4-yl)-thiazole-4-carbaldehyde 
• 190523-42-3 ethyl 2-((4S,5R)-5-methyl-2-oxooxazolidin-4-yl)thiazole-4-carboxylate 
• 70-23-5 ethyl Bromopyruvate 
• 405224-74-0 4-Methyl-benzenesulfinic acid 1-[2-((4S,5R)-5-methyl-2-oxo-oxazolidin-4-yl)-thiazol-4-yl]-meth-(E)-ylideneamide 
• 405224-70-6 C₁₆H₁₇N₃O₄S₂ 
• 405224-67-1 (2S,5R)-2,5-Bis-thiocarbamoyl-pyrrolidine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthetic studies on the thiostrepton family of peptide antibiotics: Synthesis of the tetrasubstituted dehydropiperidine and piperidine cores

The tetrasubstituted dehydropiperidine and piperidine cores of the thiostrepton family of peptide antibiotics were synthesized which featured the coupling between the azomethine ylide and the enantiopure sulfinimine, and the subsequent stereoselective reduction of the six-membered imine.