Related Experiment Video
Updated: Jun 17, 2026

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
Published on: June 20, 2014
Synthesis and antiviral activity of scopadulane-rearranged diterpenes
Miguel A González1, Lee Agudelo, Liliana Betancur-Galvis
1Departamento de Química Orgánica, Universidad de Valencia, Dr Moliner 50, E-46100 Burjassot, Valencia, Spain. miguel.a.gonzalez@uv.es <miguel.a.gonzalez@uv.es>
Abstract:
A new bioactive diterpene skeleton resulting from a backbone rearrangement is described. Activity of the rearranged product and several derivatives against Herpes Virus Simplex type 2 is reported.
Related Concept Videos
Antiviral Nucleoside Inhibitors
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
Inhibitors of Virion Maturation and Assembly
Inhibitors of Viral Protein Synthesis
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
Inhibitors Of Virion Release

