Literature DB >> 15654377

Reversible 1,4-cycloaddition of singlet oxygen to N-substituted 2-pyridones: 1,4-endoperoxide as a versatile chemical source of singlet oxygen.

Masakatsu Matsumoto1, Masayo Yamada, Nobuko Watanabe.   

Abstract

N-substituted pyridones (1) easily undergo singlet oxygenation to give exclusively the corresponding endoperoxides (2), which decompose to give pyridones again while liberating 1O2 in high yield.

Entities:  

Year:  2004        PMID： 15654377     DOI： 10.1039/b414845b

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  4 in total

1.  Storable, thermally activated, near-infrared chemiluminescent dyes and dye-stained microparticles for optical imaging.

Authors:  Jeffrey M Baumes; Jeremiah J Gassensmith; Jay Giblin; Jung-Jae Lee; Alexander G White; William J Culligan; W Matthew Leevy; Masaru Kuno; Bradley D Smith
Journal:  Nat Chem       Date:  2010-10-24       Impact factor: 24.427

2.  Mechanochemical generation of singlet oxygen.

Authors:  Abdurrahman Turksoy; Deniz Yildiz; Simay Aydonat; Tutku Beduk; Merve Canyurt; Bilge Baytekin; Engin U Akkaya
Journal:  RSC Adv       Date:  2020-03-02       Impact factor: 4.036

3.  Silyl-naphthalene endoperoxides as switchable sources of singlet oxygen for bactericidal activity.

Authors:  Min Qu; Nan Wu; Wanqing Jiang; Lei Wang; Mahinur S Akkaya; Engin U Akkaya
Journal:  RSC Adv       Date:  2021-05-26       Impact factor: 4.036

Review 4.  BODIPYs in PDT: A Journey through the Most Interesting Molecules Produced in the Last 10 Years.

Authors:  Miryam Chiara Malacarne; Marzia Bruna Gariboldi; Enrico Caruso
Journal:  Int J Mol Sci       Date:  2022-09-05       Impact factor: 6.208
  4 in total

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