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- W2950357277 abstract "Abstract Treatment of the dihydropyridine 5 with fluoride anion resulted in in situ formation of the allenyldiene 4 which cyclized to the azabicyclo[2.2.2]octene 9. Subsequent elaboration to the alcohol 24 and rearrangement gave norsecurinine 2. The intermediate diol 16 was converted into prenirurine 34 which upon conversion into an N-oxide rapidly rearranged to give traces of nirurine 1 and norphyllanthine 38." @default.
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- W2950357277 date "2010-08-19" @default.
- W2950357277 modified "2023-10-18" @default.
- W2950357277 title "ChemInform Abstract: Synthesis of the Securinega Alkaloids (.+-.)-Norsecurinine and (.+-.)- Nirurine from 3-Hydroxypyridine." @default.
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- W2950357277 doi "https://doi.org/10.1002/chin.199401285" @default.
- W2950357277 hasPublicationYear "2010" @default.
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