1350818-14-2

Upstream product

• 19790-60-4 3-Benzyloxypropanal 
• 1350818-12-0 (2S,3R,4S,6S)-2-(2-(benzyloxy)ethyl)-6-(hydroxymethyl)-3-methyltetrahydro-2H-pyran-4-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 955044-11-8 C₆H₁₂O₂ 

Downstream Products

• 932739-33-8 (2S,3S)-2-[(4R,5R)-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-yl]hex-5-en-3-ol 
• 1350818-16-4 C₁₈H₂₇IO₄ 
• 1350818-17-5 C₁₈H₂₆O₄ 
• 1350818-18-6 C₂₄H₃₂O₆ 
• 1350818-19-7 C₂₂H₂₈O₅ 
• 1350818-20-0 C₂₅H₃₂O₅ 
• 1350818-21-1 C₂₃H₃₀O₄ 
• 1350818-22-2 C₃₉H₅₂N₂O₉ 
• 1350818-23-3 C₃₇H₄₈N₂O₉ 
• 1350818-24-4 C₃₄H₄₄N₂O₉ 
• 162472-62-0 (3S,4S)-4-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-pentane-1,3-diol 
• 162600-54-6 cryptophycin-24 
• 436143-91-8 (3S,4S)-4-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-3-hydroxy-pentanal 
• 1350818-15-3 C₂₅H₃₄O₇S 

Relevant academic research and scientific papers

Synthesis of spiroketal fragment of ossamycin via Prins cyclization

An asymmetric synthesis of spiroketal fragment of an antitumour antibiotic, ossamycin is described. Coupling of aldehyde and alkyne fragments followed by spiroketalization has afforded the spiroketal sub unit of ossamycin. Both the sub targets were constr

Total synthesis of cryptophycin-24 (arenastatin A) via Prins cyclization

A stereoselective synthesis of fragment A of cryptophycin is achieved utilizing the versatile Prins cyclization. Subsequently, the total synthesis of cryptophycin-24 (arenastatin A) has been accomplished by coupling it with the depsipeptide subunit.