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Photosensitised biphotonic chemistry of pyrimidine derivatives.
Alzueta, Ofelia R; Cadet, Jean; Cuquerella, M Consuelo; Miranda, Miguel A.
Afiliação
  • Alzueta OR; Instituto Universitario Mixto de Tecnología Química, Universitat Politècnica de València (UPV-CSIC), Av. Los Naranjos s/n, 46022, Valencia, Spain. mcuquere@itq.upv.es mmiranda@qim.upv.es.
  • Cadet J; Prof. J. Cadet Département de Médecine Nucléaire et Radiobiologie, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
  • Cuquerella MC; Instituto Universitario Mixto de Tecnología Química, Universitat Politècnica de València (UPV-CSIC), Av. Los Naranjos s/n, 46022, Valencia, Spain. mcuquere@itq.upv.es mmiranda@qim.upv.es.
  • Miranda MA; Instituto Universitario Mixto de Tecnología Química, Universitat Politècnica de València (UPV-CSIC), Av. Los Naranjos s/n, 46022, Valencia, Spain. mcuquere@itq.upv.es mmiranda@qim.upv.es.
Org Biomol Chem ; 18(12): 2227-2232, 2020 03 25.
Article em En | MEDLINE | ID: mdl-32167122
ABSTRACT
Photosensitised biphotonic irradiation of DNA has been rarely addressed, probably due to the difficulties in the experimental design. This is associated with the selection of nucleobases and sensitisers with appropriate absorption spectra and photochemical reactivity, in combination with a laser source emitting intense UVA light of the adequate wavelength. The present paper presents a new strategy involving absorption of a first UVA photon by an adequate sensitiser followed by triplet energy transfer to a pyrimidine (Pyr) derivative and absorption of a second UVA photon by the resulting Pyr triplet excited state. The feasibility of the proposed strategy has been demonstrated using two model reactions (i) the Norrish-Yang photocyclisation of a tert-butyluracil and (ii) the photohydration of its uracil analogue, lacking the tert-butyl substituent.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article