The synthesis and acid-catalysed rearrangement of a spiro[4,5]dec-6-en-2-one
Abstract
The spiro[4,5]dec-6-en-2-one (3) has been synthesized and found to undergo rearrangement into the octalone (4) upon acid treatment.
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Article information
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J. Chem. Soc. D, 1970, 1232-1233
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The synthesis and acid-catalysed rearrangement of a spiro[4,5]dec-6-en-2-one
D. Caine and J. B. Dawson, J. Chem. Soc. D, 1970, 1232 DOI: 10.1039/C29700001232
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