Issue 5, 2004

Synthesis of photochromic 2,3-bis(2,5-dimethyl-3-thienyl)-3-cyanoacrylates by the Beckmann rearrangement of a cyclobutenedione derivative

Abstract

An unusual Beckmann rearrangement was discovered in the reaction of 3,4-bis(2,5-dimethyl-3-thienyl)cyclobut-3-ene-1,2-dione with hydroxylamine hydrochloride to give esters of 2,3-bis(2,5-dimethyl-3-thienyl)-3-cyanoacrylic acid.

Article information

Article type
Communication
Submitted
15 Mar 2004

Mendeleev Commun., 2004,14, 202-204

Synthesis of photochromic 2,3-bis(2,5-dimethyl-3-thienyl)-3-cyanoacrylates by the Beckmann rearrangement of a cyclobutenedione derivative

V. Z. Shirinian, M. M. Krayushkin, V. A. Barachevskii, L. I. Belen'kii, A. A. Shimkin and Y. P. Strokach, Mendeleev Commun., 2004, 14, 202 DOI: 10.1070/MC2004v014n05ABEH001916

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