corrole and 4-4-difluoro-4-bora-3a-4a-diaza-s-indacene

corrole has been researched along with 4-4-difluoro-4-bora-3a-4a-diaza-s-indacene* in 1 studies

Other Studies

1 other study(ies) available for corrole and 4-4-difluoro-4-bora-3a-4a-diaza-s-indacene

Article	Year
Nucleophilic Aromatic Substitution on Pentafluorophenyl-Substituted Dipyrranes and Tetrapyrroles as a Route to Multifunctionalized Chromophores for Potential Application in Photodynamic Therapy. Chemistry (Weinheim an der Bergstrasse, Germany), 2016, Sep-19, Volume: 22, Issue:39 The application of porphyrinoids in biomedical fields, such as photodynamic therapy (PDT), requires the introduction of functional groups to tune their solubility for the biological environment and to allow a coupling to other active moieties or carrier systems. A valuable motif in this regard is the pentafluorophenyl (PFP) substituent, which can easily undergo a regiospecific nucleophilic replacement (S Topics: Amines; Benzaldehydes; Boron Compounds; Cell Line, Tumor; Chemistry Techniques, Synthetic; Halogenation; Humans; Models, Molecular; Neoplasms; Photochemotherapy; Photosensitizing Agents; Porphyrins; Pyrroles; Tetrapyrroles	2016

Article

Year

Nucleophilic Aromatic Substitution on Pentafluorophenyl-Substituted Dipyrranes and Tetrapyrroles as a Route to Multifunctionalized Chromophores for Potential Application in Photodynamic Therapy.

Chemistry (Weinheim an der Bergstrasse, Germany), 2016, Sep-19, Volume: 22, Issue:39

The application of porphyrinoids in biomedical fields, such as photodynamic therapy (PDT), requires the introduction of functional groups to tune their solubility for the biological environment and to allow a coupling to other active moieties or carrier systems. A valuable motif in this regard is the pentafluorophenyl (PFP) substituent, which can easily undergo a regiospecific nucleophilic replacement (S

Topics: Amines; Benzaldehydes; Boron Compounds; Cell Line, Tumor; Chemistry Techniques, Synthetic; Halogenation; Humans; Models, Molecular; Neoplasms; Photochemotherapy; Photosensitizing Agents; Porphyrins; Pyrroles; Tetrapyrroles

2016