Issue 16, 1984

Intramolecular thermal oxidoreduction of N-(2-hydroxypropyl)-β-enaminoesters: synthesis of N-(acetonyl)-β-enaminoaldehydes and 2-acetylpyrroles

Abstract

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1135-1136

Intramolecular thermal oxidoreduction of N-(2-hydroxypropyl)-β-enaminoesters: synthesis of N-(acetonyl)-β-enaminoaldehydes and 2-acetylpyrroles

A. Maujean, C. Grosdemange-Pale, G. Marcy and J. Chuche, J. Chem. Soc., Chem. Commun., 1984, 1135 DOI: 10.1039/C39840001135

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements