Issue 16, 2007
From the journal:

Organic & Biomolecular Chemistry

Synthetic routes to 3-alkylsulfanyl-6-aryl-diketopyrrolo[3,4-c]pyrroles—a class of efficient, visible light excitable fluorophores

Bert Metten,a   Karen Martinez,a   Joice Thomas,a   Wenwu Qin,a   Mario Smet,a   Noël Boensa  and  Wim Dehaen*a  

* Corresponding authors

a Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200F, Box 02404, Leuven, Belgium
E-mail: Wim.Dehaen@chem.kuleuven.be
Fax: +32 16 32 7990
Tel: +32 16 32 7439

Abstract

Sulfide derivatives of diketopyrrolo[3,4-c]pyrrole (SDPPs) were prepared in a one-pot procedure from arylpyrrolinones, isothiocyanates and alkylating agents, and their properties as fluorophores were evaluated.

Graphical abstract: Synthetic routes to 3-alkylsulfanyl-6-aryl-diketopyrrolo[3,4-c]pyrroles—a class of efficient, visible light excitable fluorophores

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B707281C
Article type
Paper
Submitted
15 May 2007
Accepted
19 Jun 2007
First published
04 Jul 2007

Org. Biomol. Chem., 2007,5, 2587-2591

Permissions

Request permissions

Synthetic routes to 3-alkylsulfanyl-6-aryl-diketopyrrolo[3,4-c]pyrroles—a class of efficient, visible light excitable fluorophores

B. Metten, K. Martinez, J. Thomas, W. Qin, M. Smet, N. Boens and W. Dehaen, Org. Biomol. Chem., 2007, 5, 2587 DOI: 10.1039/B707281C

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