Intramolecular Thermal Oxidoreduction of N-(2-Hydroxypropyl)-β-enaminoesters: Synthesis of N-(Acetonyl)-β-enaminoaldehydes and 2-Acetylpyrroles

DOI: 10.1039/c39840001135

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1135 - 1136 (1984)

Update date:2022-07-29

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Authors:

Maujean, Alain

Grosdemange-Pale, Catherine

Marcy, Guy

Chuche, Josselin

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Article abstract of DOI:10.1039/c39840001135

Flow pyrolysis of the β-enaminoesters (1) provides the enaminoaldehydes (2), resulting from intramolecular oxidoreduction, and the acetylpyrroles (3); their relative yields depend on the temperature range.

Full text of DOI:10.1039/c39840001135

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