Issue 3, 1984

Oxyanion-assisted retro-Diels–Alder reactions in the tricyclo[3.3.02,8]nona-3,6-diene (barbaralane) system

Abstract

9-Vinyl- and 9-aryl-tricyclo[3.3.1.02,8]nona-3,6-dien-9-olates (1ch) underwent the retro-Diels-Alder reaction to give cycloheptrienes (2ch) in excellent yields, indicating that it is not necessary for the fragmented 4π component to be incorporated into an aromatic nucleus.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 179-180

Oxyanion-assisted retro-Diels–Alder reactions in the tricyclo[3.3.02,8]nona-3,6-diene (barbaralane) system

T. Miyashi, A. Ahmed and T. Mukai, J. Chem. Soc., Chem. Commun., 1984, 179 DOI: 10.1039/C39840000179

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