130253-46-2

Upstream product

• 2552-93-4 C₂₂H₃₂N₄O 
• 501-53-1 benzyl chloroformate 
• 4360-12-7 (+)-ajmaline 
• 2552-93-4 C₂₂H₃₂N₄O 

Downstream Products

• 141810-23-3 C₃₄H₄₄N₂O₄Si 
• 141810-23-3 C₃₄H₄₄N₂O₄Si 
• 141810-26-6 C₅₀H₆₄N₂O₄Si₂ 
• 141810-21-1 C₄₀H₆₀N₂O₄Si₂ 
• 141810-22-2 C₃₄H₄₅BrN₂O₄Si 
• 141810-27-7 C₃₄H₄₈N₂O₅Si 
• 141810-25-5 C₃₄H₄₆N₂O₄Si 
• 141810-29-9 C₂₈H₃₂N₂O₅ 
• 141810-28-8 C₂₈H₃₄N₂O₅ 
• 130253-45-1 C₃₄H₄₆N₂O₄Si 
• 130253-28-0 C₂₈H₃₂N₂O₄ 
• 130253-28-0 C₂₈H₃₂N₂O₄ 

Relevant academic research and scientific papers

Structure and Synthesis of a New Indole Alkaloid, 19(S)-Hydroxy-Nb-methylraumacline, Obtained by the Biotransformation of Ajmaline in Plant Cell Cultures of Rauwolfia Serpentina Benth.

From the plant cell suspension cultures of Rauwolfia serpentina Benth., which were cultivated in the alkaloid-production medium after feeding of ajmaline (1), a new indole alkaloid 19-(S)-hydroxy-Nb-methylraumacline (4) was isolated.The structu

Synthetic studies on gelsedine alkaloids-I: Stereoselective preparation of hypothetical biogenetic intermediates, D-Norsarpagine type compounds from ajmaline

D-Norsarpagine type compound (4) and its C/D ring-opening derivative (22), which were corresponding to the hypothetical biogenetic intermediate for gelsedine (6), were prepared from ajmaline (3) via the deformylation (C21) and the construction