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Sulfonylative and Azidosulfonylative Cyclizations by Visible-Light-Photosensitization of Sulfonyl Azides in THF.
Zhu, Shaoqun; Pathigoolla, Atchutarao; Lowe, Grace; Walsh, Darren A; Cooper, Mick; Lewis, William; Lam, Hon Wai.
Afiliación
  • Zhu S; The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.
  • Pathigoolla A; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
  • Lowe G; The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.
  • Walsh DA; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
  • Cooper M; The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.
  • Lewis W; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
  • Lam HW; The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.
Chemistry ; 23(69): 17598-17604, 2017 Dec 11.
Article en En | MEDLINE | ID: mdl-28945301
ABSTRACT
The generation of sulfonyl radicals from sulfonyl azides using visible light and a photoactive iridium complex in THF is described. This process was used to promote sulfonylative and azidosulfonylative cyclizations of enynes to give several classes of highly functionalized heterocycles. The use of THF as the solvent is critical for successful reactions. The proposed mechanism of radical initiation involves the photosensitized formation of a triplet sulfonyl nitrene, which abstracts a hydrogen atom from THF to give a tetrahydrofuran-2-yl radical, which then reacts with the sulfonyl azide to generate the sulfonyl radical.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido