852310-63-5

Upstream product

• 2746-25-0 p-Methoxybenzyl bromide 
• 852310-61-3 Formic acid (1S,2R)-2-(4-methoxy-benzyloxy)-1-methyl-3-oxo-propyl ester 
• 852310-62-4 3-(4-methoxybenzyloxy)-5-(4-methoxyphenyl)-(2S,3S,4E)-4-penten-2-ol 
• 852310-57-7 2-(4-methoxybenzyloxy)-4-(4-methoxyphenyl)-1-methyl-(1S,2S,3E)-3-butenyl formate 
• 852310-58-8 6-(4-methoxybenzyloxy)-2,2,5-trimethyl-(3aS,5S,6R,6aS)-perhydrofurol[2,3-d][1,3]dioxole 
• 852310-60-2 4-(4-methoxybenzyloxy)-5-methyl-(3S,4R,5S)-tetrahydro-2,3-furandiol 
• 906478-67-9 Methanesulfonic acid (E)-(1S,2S)-2-(4-methoxy-benzyloxy)-4-(4-methoxy-phenyl)-1-methyl-but-3-enyl ester 

Downstream Products

• 852310-64-6 4-azido-1-(4-methoxyphenyl)-(E,3S,4R)-1-penten-3-ol 
• 852310-56-6 2-[tert-butoxycarbonylamino]-(2R,3S,4E)-5-(4-methoxyphenyl)-pent-4-en-3-ol 
• 906478-68-0 (E)-(3S,4R)-4-Amino-1-(4-methoxy-phenyl)-pent-1-en-3-ol 

Relevant academic research and scientific papers

Practical and highly stereoselective approaches to the total synthesis of (-)-codonopsinine

The enantiopure total synthesis of (-)-codonopsinine is described using two effective chiron approaches starting either from commercially available l-xylose or from readily available Garner aldehyde. The key steps included Julia trans-olefination, highly

Total synthesis of the alkaloid (-)-codonopsinine from L-xylose

The enantiopure total synthesis of (-)-codonopsinine is described from commercially available L-xylose in 20% overall yield. The key steps included Julia trans olefination and cascade epoxidation-cyclisation strategies.