436143-91-8

Upstream product

• 162472-62-0 (3S,4S)-4-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-pentane-1,3-diol 
• 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 
• 436143-83-8 2-methyl-7-phenyl-6,8-dioxabicyclo[3.2.1]octan-3-ol 
• 207558-04-1 methyl 2-(1'-ethoxyethoxy)-2-phenyl acetate 
• 133187-19-6 (R)-2-(1-ethoxyethoxy)-2-phenylacetaldehyde 
• 20698-91-3 (R)-methyl mandelate 

Downstream Products

• 436143-85-0 (E)-(5S,6S)-6-((4R,5R)-2,2-Dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-5-hydroxy-hept-2-enoic acid allyl ester 
• 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 
• 436143-88-3 2-(3-tert-butoxycarbonylamino-2-methyl-propionyloxy)-4-methyl-pentanoic acid 4-[2-(3-chloro-4-methoxy-phenyl)-1-(2,2,2-trichloro-ethoxycarbonyl)-ethylcarbamoyl]-1-[1-(2,2-dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-ethyl]-but-3-enyl ester 
• 436143-87-2 (R)-3-(3-Chloro-4-methoxy-phenyl)-2-[(E)-(5S,6S)-6-((4R,5R)-2,2-dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-5-hydroxy-hept-2-enoylamino]-propionic acid 2,2,2-trichloro-ethyl ester 
• 436143-89-4 (5S,6S,E)-6-[(4R,5R)-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-yl]-5-hydroxyhept-2-enoic acid 
• 196794-26-0 (E)-(3S,6R,10R,16S)-10-(3-Chloro-4-methoxy-benzyl)-16-((1R,2R,3R)-2,3-dihydroxy-1-methyl-3-phenyl-propyl)-3-isobutyl-6-methyl-1,4-dioxa-8,11-diaza-cyclohexadec-13-ene-2,5,9,12-tetraone 
• 124689-65-2 cryptophycin-1 

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.

Stereospecific synthesis of cryptophycin 1

Matrix presented A brief stereospecific synthesis of cryptophycin 1 is described in which (R)-mandelic acid serves as the sole source of asymmetry for unit A. The key step is a hetero-Diels-Alder cycloaddition.