Issue 5, 1999
From the journal:

Chemical Communications

A new synthetic path to peri-naphthisoxazoles by oxidative intramolecular cyclization of some β,γ-unsaturated oximes

John C. Barnes,   William M. Horspool  and  George Hynd  

Abstract

Some β,γ-unsaturated oximes undergo an unprecedented intramolecular cycloaddition to an aryl group to afford peri-naphthisoxazoles when they are irradiated in the presence of PhI(OAc)2 and I2 or HgO and I2 in benzene or by thermal reaction with NaOCl and Et3N in CH2Cl2.

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/A809610D
Article type
Paper

Chem. Commun., 1999, 425-426

Permissions

Request permissions

A new synthetic path to peri-naphthisoxazoles by oxidative intramolecular cyclization of some β,γ-unsaturated oximes

J. C. Barnes, W. M. Horspool and G. Hynd, Chem. Commun., 1999, 425 DOI: 10.1039/A809610D

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.

Social activity

Spotlight

Advertisements