Jump to main content
Jump to site search


Biaryl sulfonamides as cisoid azosteres for photopharmacology

Author affiliations

Abstract

Biaryl sulfonamides are excellent candidates for the azologization approach that yields photoswitchable drugs more active in their metastable cis state, compared to the stable trans state. Here we present the scope and limitations of this strategy for rational design in photopharmacology.

Graphical abstract: Biaryl sulfonamides as cisoid azosteres for photopharmacology

Back to tab navigation

Supplementary files

Article information


Submitted
19 Feb 2021
Accepted
17 Mar 2021
First published
18 Mar 2021

This article is Open Access

Chem. Commun., 2021, Advance Article
Article type
Communication

Biaryl sulfonamides as cisoid azosteres for photopharmacology

P. Kobauri, W. Szymanski, F. Cao, S. Thallmair, S. J. Marrink, M. D. Witte, F. J. Dekker and B. L. Feringa, Chem. Commun., 2021, Advance Article , DOI: 10.1039/D1CC00950H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Material from this article can be used in other publications provided that the correct acknowledgement is given with the reproduced material and it is not used for commercial purposes.

Reproduced material should be attributed as follows:

  • For reproduction of material from NJC:
    [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the Centre National de la Recherche Scientifique (CNRS) and the RSC.
  • For reproduction of material from PCCP:
    [Original citation] - Published by the PCCP Owner Societies.
  • For reproduction of material from PPS:
    [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the European Society for Photobiology, the European Photochemistry Association, and RSC.
  • For reproduction of material from all other RSC journals:
    [Original citation] - Published by The Royal Society of Chemistry.

Information about reproducing material from RSC articles with different licences is available on our Permission Requests page.


Social activity

Search articles by author

Spotlight

Advertisements