Thioenamide Photochemistry

DOI: 10.1039/c39820000842

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 842 - 843 (1982)

Update date:2022-08-02

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Authors:

Couture, Axel

Dubiez, Regine

Lablache-Combier, Alain

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Article abstract of DOI:10.1039/c39820000842

In contrast with their oxo-analogues, thioenamides undergo photochemical cyclization to yield isoquinolinethione derivatives which are easily converted into isoquinolones and tetrahydroisoquinolines by treatment with benzeneseleninic anhydride and EtO3BF4

Full text of DOI:10.1039/c39820000842

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