Issue 22, 1995

Gas-phase pyrolysis of 2,3-dihydro-1,4-diazepines: involvement of the saturated portion of the ring in chemical reactions and novel cistrans isomerisation of a fused ring system

Abstract

Flash vacuum pyrolysis of 2,3-dihydro-1,4-diazepines in the range 450–550 °C involves interaction of the saturated portion of the molecule with the vinamidine system and causes 1,5-hydrogen shifts which have been established by deuterium labelling experiments; at higher temperatures, ring contraction occurs to give pyrazines as major products.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2337-2338

Gas-phase pyrolysis of 2,3-dihydro-1,4-diazepines: involvement of the saturated portion of the ring in chemical reactions and novel cistrans isomerisation of a fused ring system

M. J. Ellis, D. Lloyd, H. McNab and M. J. Walker, J. Chem. Soc., Chem. Commun., 1995, 2337 DOI: 10.1039/C39950002337

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