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Intramolecular interception of the Newman-Kwart rearrangement by carboxylic acids

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posted on 2024-11-15, 21:06 authored by Timothy Ablott, Mitchell Fishburn, David Turner, Christopher RichardsonChristopher Richardson
© 2020 Elsevier Ltd Instead of undergoing the Newman-Kwart rearrangement, thermally-promoted reactions of O-aryl dimethylthiocarbamates featuring ortho-carboxylic acid substituents result in the loss of carbonylsulfide and formation of N,N-dimethylsalicylamides in high yields.

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Citation

Ablott, T., Fishburn, M., Turner, D. & Richardson, C. (2020). Intramolecular interception of the Newman-Kwart rearrangement by carboxylic acids. Tetrahedron Letters,

Language

English

RIS ID

144107

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