Published in

Royal Society of Chemistry, New Journal of Chemistry, 22(44), p. 9444-9451, 2020

DOI: 10.1039/d0nj01605e

Links

Tools

Export citation

Search in Google Scholar

Fast and easy conversion of ortho amidoaryldiselenides into the corresponding Ebselen-like derivatives driven by theoretical investigations.

Journal article published in 2020 by Vanessa Nascimento ORCID, Pâmella da Silva Cordeiro, Pâmella Silva Cordeiro, Massimiliano Arca ORCID, Francesca Marini ORCID, Luca Sancineto ORCID, Antonio Luiz Braga ORCID, Vito Lippolis ORCID, Michio Iwaoka ORCID, Claudio Santi ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Upload
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

Abstract

The in silico predicted Se⋯N interaction on amidoarylselenenyl iodides has been experimentally exploited for the efficient synthesis of N-substituted benzoisoselenazol-3(2H)-ones, benzoisothiazol-3(2H)-ones and ebselen, recently reported as potent antiviral agent against Sars-Cov2.