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- W2950582016 abstract "Abstract A new, short and efficient route to louisianins C and D is described in which the pyridine ring is constructed from a disubstituted 1,2,4-triazine by an inverse-electron-demand Diels–Alder/retro-Diels–Alder/aromatisation cascade sequence. This eight-step route produces louisianin C in 16% overall yield from the commercially available 5-chloropent-1-yne." @default.
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- W2950582016 date "2008-08-12" @default.
- W2950582016 modified "2023-09-26" @default.
- W2950582016 title "ChemInform Abstract: An Efficient 1,2,4-Triazine-Based Route to the Louisianin Alkaloids." @default.
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- W2950582016 doi "https://doi.org/10.1002/chin.200833200" @default.
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