Issue 60, 2020

Exploring an anomaly: the synthesis of 7,7′-diazaindirubin through a 7-azaindoxyl intermediate

Abstract

Two independent methods generating 7-azaindoxyl as an intermediate verify that 7,7′-diazaindirubin is formed exclusively over 7,7′-diazaindigo. This contrasts with long-standing knowledge related to the reactivity of indoxyl, which proceeds via a radical-initiated homodimerization process, leading to indigo. A series of experiments confirms 7-azaindoxyl as an intermediate with results suggesting a condensation pathway followed by oxidation.

Graphical abstract: Exploring an anomaly: the synthesis of 7,7′-diazaindirubin through a 7-azaindoxyl intermediate

Supplementary files

Article information

Article type
Paper
Submitted
19 Aug 2020
Accepted
24 Sep 2020
First published
06 Oct 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 36849-36852

Exploring an anomaly: the synthesis of 7,7′-diazaindirubin through a 7-azaindoxyl intermediate

J. A. Shriver, K. R. Wang, A. C. Patterson, J. R. DeYoung and R. J. Lipsius, RSC Adv., 2020, 10, 36849 DOI: 10.1039/D0RA07144G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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