1332569-85-3

Upstream product

• 89426-28-8 (2R,3R)-2,3-epoxypent-4-yn-1-ol 
• 35042-52-5 (E)-2-penten-4-yn-1-ol 

Downstream Products

• 1332569-96-6 (S)-tert-butyl 4-((R)-1-(benzoyloxy)-3-(4-heptylphenyl)prop-2-ynyl)-2-oxooxazolidine-3-carboxylate 
• 1332570-05-4 C₁₈H₂₉NO₂ 
• 1332570-04-3 N-((2S,3R,E)-5-(4-heptylphenyl)-1,3-dihydroxypent-4-en-2-yl)octanamide 
• 1332570-00-9 tert-butyl (2S,3R,E)-5-(4-heptyphenyl)-1,3-dihydroxypent-4-en-2-ylcarbamate 
• 1332569-98-8 tert-butyl (2S,3R)-5-(4-heptylphenyl)-1,3-dihydroxypent-4-yn-2-ylcarbamate 

Relevant academic research and scientific papers

Enantioselective synthesis of sphingadienines and aromatic ceramide analogs

A new approach to the synthesis of sphingoid bases has been developed. The strategy is based on Sonogashira coupling of a chiral acetylenic carbamate that can be prepared in enantiomerically enriched form from 2,3-epoxy-4-pentyn-1-ol, which is readily acc