Issue 0, 1974

Aryne chemistry. Part XXXVI. Approaches to the synthesis of 5,6,7,8-tetrahalogeno-1,4-dihydro-2-nitroso-1,4-ethenonaphthalenes (2-nitrosotetrahalogenobenzobarrelenes)

Abstract

The reactions of arynes, generated by aprotic diazotisation of the corresponding anthranilic acids, with nitrosoarenes gave N-hydroxycarbazole derivatives. 1,4-Dihydro-2-nitroso-1,4-ethenonaphthalene derivatives were implicated in reactions of 3-bromo-3,4-dihydro-1,4-ethenonaphthalen-2(1H)-one oximes with triethylamine, which led to the expected naphthalene derivatives.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 2695-2697

Aryne chemistry. Part XXXVI. Approaches to the synthesis of 5,6,7,8-tetrahalogeno-1,4-dihydro-2-nitroso-1,4-ethenonaphthalenes (2-nitrosotetrahalogenobenzobarrelenes)

P. C. Buxton, H. Heaney, K. G. Mason and J. M. Sketchley, J. Chem. Soc., Perkin Trans. 1, 1974, 2695 DOI: 10.1039/P19740002695

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