Issue 6, 1970

Heterocyclic analogues of cyclopentadienylidenecycloheptatriene derived from 1,3,4-oxadiazole and 1,2,4-triazole

Abstract

Heterocyclic systems having the same π-electron configuration as cyclopentadienylidenecycloheptatriene are of two types, covalent and dipolar. The stable covalent 2-fluoren-9-ylidene-3,5-dimethyl-Δ4-1,3,4-oxadiazoline (10) and 5-fluoren-9-ylidene-1,3,4-trimethyl-Δ2-1,2,4-triazoline (15) have been prepared starting with fluorene-9-carbohydrazide. The synthesis of the unstable dipolar anhydro-5-fluoren-9-yl-2,3-diphenyl-1,3,4-oxadiazolium hydroxide (20) and attempts to obtain its 5-diphenylmethyl analogue are described.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 807-810

Heterocyclic analogues of cyclopentadienylidenecycloheptatriene derived from 1,3,4-oxadiazole and 1,2,4-triazole

G. V. Boyd and M. D. Harms, J. Chem. Soc. C, 1970, 807 DOI: 10.1039/J39700000807

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