Synthesis of isoindole by retro-Diels–Alder reaction
Abstract
Thermal fragmentation of 1,2,3,4-tetrahydro-1,4-epiminonaphthalene at reduced pressure affords pure isoindole in essentially quantitative yield.
Please wait while we load your content...
Article information
- Article type
- Paper
J. Chem. Soc., Chem. Commun., 1972, 1149-1150
Permissions
Synthesis of isoindole by retro-Diels–Alder reaction
J. Bornstein, D. E. Remy and J. E. Shields, J. Chem. Soc., Chem. Commun., 1972, 1149 DOI: 10.1039/C39720001149
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.