Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 44, 2015
Previous Article Next Article

Exploiting amphiphilicity: facile metal free access to thianthrenes and related sulphur heterocycles

Author affiliations

Abstract

Benzodithioloimines are reacted with arynes or alkynes substituted with electron-withdrawing groups to afford the corresponding thianthrene or benzo[b][1,4]dithiine derivatives. The transformation takes place under mild reaction conditions without any transition metal. Furthermore, the reaction mode could be expanded to 2-thiocyanatopyrroles yielding pyrrolothiazoles.

Graphical abstract: Exploiting amphiphilicity: facile metal free access to thianthrenes and related sulphur heterocycles

Back to tab navigation

Supplementary files

Article information


Submitted
28 Feb 2015
Accepted
28 Apr 2015
First published
28 Apr 2015

This article is Open Access

Chem. Commun., 2015,51, 9165-9168
Article type
Communication

Exploiting amphiphilicity: facile metal free access to thianthrenes and related sulphur heterocycles

M. Pawliczek, L. K. B. Garve and D. B. Werz, Chem. Commun., 2015, 51, 9165
DOI: 10.1039/C5CC01757B

This article is licensed under a Creative Commons Attribution 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.

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