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- W2080606798 abstract "Abstract The efficient synthesis of an A-ring synthon for the marine hepatatoxin cylindrospermopsin has been achieved. The key step features an intramolecular oxazinone N-oxide/alkene dipolar cycloaddition resulting in the establishment of the three contiguous stereogenic centers in the A-ring from one pre-existing stereogenic center in a single step." @default.
- W2080606798 created "2016-06-24" @default.
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- W2080606798 date "2001-05-08" @default.
- W2080606798 modified "2023-09-27" @default.
- W2080606798 title "ChemInform Abstract: Construction of the A-Ring of Cylindrospermopsin via an Intramolecular Oxazinone-N-oxide Dipolar Cycloaddition." @default.
- W2080606798 cites W2952860440 @default.
- W2080606798 doi "https://doi.org/10.1002/chin.200119198" @default.
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