Cookies Policy

This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies.

I accept this policy

Find out more here

Photoinduced Electron Transfer Oxygenations of 4-Arylmethylene-1,3(2H,4H)-Isoquinolinediones Via Their Anion Radical Intermediates

No metrics data to plot.
The attempt to load metrics for this article has failed.
The attempt to plot a graph for these metrics has failed.
The full text of this article is not currently available.

Brill’s MyBook program is exclusively available on BrillOnline Books and Journals. Students and scholars affiliated with an institution that has purchased a Brill E-Book on the BrillOnline platform automatically have access to the MyBook option for the title(s) acquired by the Library. Brill MyBook is a print-on-demand paperback copy which is sold at a favorably uniform low price.

This Article is currently unavailable for purchase.
Add to Favorites
You must be logged in to use this functionality

Cover image Placeholder

Photoinduced Electron Transfer Oxygenations of 4-Arylmethylene-1,3(2H,4H)-isoquinolinediones afforded oxiranes (5a-5c, 6a-6c, 7) and 1, 3, 4-isoquinolinetriones (8 and 9) as major products in high yields in the presence of triethylamine (TEA). These oxygenation reactions are initiated by single electron transfer between photoexcited 4-Arylmethylene-1,3(2H,4H)-isoquinolinediones and TEA, and proceeded via the anion radicals of the substrates.

Affiliations: 1: Department of Chemistry, Nanjing University, Nanjing 210093, P. R. CHINA


Full text loading...


Data & Media loading...

Article metrics loading...



Can't access your account?
  • Key

  • Full access
  • Open Access
  • Partial/No accessInformation