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- W2152317610 abstract "The thermolysis of an N-methylacetamido cyclopropane, spiro-substituted by a benzofuran-3-one moiety, was found to result in the elimination of methylamine and the formation of the correspondingly spiro-substituted cyclopentenone. The structures of starting material and product were determined by single-crystal X-ray diffraction methods and a mechanism for the elimination/ring enlargement reaction is proposed on the basis of the X-ray results." @default.
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- W2152317610 date "1984-01-01" @default.
- W2152317610 modified "2023-09-27" @default.
- W2152317610 title "Thermolytic conversion of an acetamido-substituted cyclopropane into a cyclopentenone. Crystal and molecular structures of 2-Spiro-substituted Benzofuran-3-ones" @default.
- W2152317610 cites W625827176 @default.
- W2152317610 doi "https://doi.org/10.1071/ch9842225" @default.
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