162472-62-0

Upstream product

• 162472-61-9 (E)-(S)-4-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-pent-2-en-1-ol 
• 1350818-14-2 ((2S,4S,5R,6S)-6-(2-(benzyloxy)ethyl)-4-hydroxy-5-methyltetrahydro-2H-pyran-2-yl)methyl-4-methylbenzenesulfonate 
• 1350818-12-0 (2S,3R,4S,6S)-2-(2-(benzyloxy)ethyl)-6-(hydroxymethyl)-3-methyltetrahydro-2H-pyran-4-ol 
• 1350818-21-1 C₂₃H₃₀O₄ 
• 1350818-20-0 C₂₅H₃₂O₅ 
• 1350818-19-7 C₂₂H₂₈O₅ 
• 1350818-18-6 C₂₄H₃₂O₆ 
• 1350818-17-5 C₁₈H₂₆O₄ 
• 1350818-16-4 C₁₈H₂₇IO₄ 
• 1350818-15-3 C₂₅H₃₄O₇S 
• 162472-60-8 (E)-(S)-4-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-pent-2-enoic acid methyl ester 

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 
• 1350818-22-2 C₃₉H₅₂N₂O₉ 
• 1350818-23-3 C₃₇H₄₈N₂O₉ 
• 1350818-24-4 C₃₄H₄₄N₂O₉ 
• 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 
• 162472-63-1 C₂₇H₂₈O₆ 
• 1028275-49-1 C₃₀H₃₂O₆ 

Relevant academic research and scientific papers

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.

The absolute stereostructure of arenastatin A, a potent cytotoxic depsipeptide from the Okinawan marine sponge Dysidea arenaria

The absolute stereostructure of arenastatin A (1), which was isolated from the Okinawan marine sponge Dysidea arenaria, has been determined on the bases of NMR and synthetic studies. Arenastatin A (1) is a cyclic depsipeptide exhibiting extremely potent c