1380508-49-5

Upstream product

• 1448608-16-9 (3aS,4R,5R,7aS)-7-iodo-4-methoxy-2,2-dimethyl-3a,4,5,7a-tetrahydrobenzo[d][1,3]dioxol-5-ol 
• 1448608-15-8 (((3aS,4S,5R,7aS)-7-iodo-4-methoxy-2,2-dimethyl-3a,4,5,7a-tetrahydrobenzo[d][1,3]dioxol-5-yl)oxy)triisopropylsilane 
• 1448608-14-7 C₁₈H₃₃IO₄Si 
• 165611-18-7 (3aS,4R,5R,7aS)-7-iodo-2,2-dimethyl-3a,4,5,7a-tetrahydro-1,3-benzodioxole-4,5-diol 
• 154784-39-1 (3aS,7aS)-4-iodo-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 138769-92-3 cis-(1S,2S)-1,2-dihydroxy-3-iodocyclohexa-3,5-diene 
• 1448608-18-1 C₂₉H₄₈O₄Si 
• 1448608-17-0 1,2-O,O′-isopropylidenephomentrioloxin 
• 36602-33-2 2-(4-methyl-3-pentenyl)-1-buten-3-yne 

Downstream Products

• 1448608-19-2 1,2,4-O,O′,O″-triacetylphomentrioloxin 
• 1380317-53-2 1,2,4-tri-O-acetylphomentrioloxin 

Relevant academic research and scientific papers

Chemoenzymatic total synthesis of the phytotoxic geranylcyclohexentriol (-)-phomentrioloxin

The enantiomeric form, 1R, of the structure (1S) assigned to the phytotoxic natural product phomentrioloxin has been synthesized in seven steps from the homochiral cis-1,2-dihydrocatechol 3. These studies reveal that the true structure of phomentrioloxin