138089-52-8

Upstream product

• 109-00-2 3-HYDROXYPYRIDINE 
• 138060-49-8 C₁₇H₂₃NO₅ 
• 138060-44-3 (1R,7S,9S)-3-Oxo-9-[3-(toluene-4-sulfonyloxy)-propyl]-2-oxa-8-aza-tricyclo[5.2.2.0^1,5]undeca-4,10-diene-8-carboxylic acid methyl ester 
• 138060-41-0 2-Allyl-3-(4-trimethylsilanyl-but-2-ynoyloxy)-2H-pyridine-1-carboxylic acid methyl ester 
• 138060-43-2 (1S,7R,9R)-9-(3-Hydroxy-propyl)-3-oxo-2-oxa-8-aza-tricyclo[5.2.2.0^1,5]undeca-4,10-diene-8-carboxylic acid methyl ester 
• 138060-42-1 (1S,7R,9R)-9-Allyl-3-oxo-2-oxa-8-aza-tricyclo[5.2.2.0^1,5]undeca-4,10-diene-8-carboxylic acid methyl ester 
• 138060-46-5 dihydroxynirurine 
• 138060-45-4 desoxadehydronirurine 
• 138060-40-9 4-Trimethylsilanyl-but-2-ynoic acid pyridin-3-yl ester 
• 135192-53-9 pentafluorophenoxythiocarbonyl chloride 
• 138060-49-8 C₁₇H₂₃NO₅ 

Downstream Products

• 2650-35-3 (+/-)-norsecurinine 

Relevant academic research and scientific papers

Synthesis of the Securinega Alkaloids (+/-)-Norsecurinine and (+/-)-Nirurine from 3-Hydroxypyridine

Treatment of the dihydropyridine 5 with fluoride anion resulted in in situ formation of the allenylidene 4 which cyclized to the azabicyclooctene 9.Subsequent elaboration to the alcohol 24 and rearrangement gave norsecurinine 2.The intermediate dio