Photoreaction of arenecarbothioamides with 2-vinylfuran analogues. The formation of tetracyclic indoles and 2,3-diaryl-2-pyrrolin-5-ones

DOI: 10.1248/cpb.46.1522

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1522 - 1526 (1998)

Update date:2022-08-03

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Authors:

Oda, Kazuaki

Tsujita, Hisao

Sakai, Masayuki

Machida, Minoru

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Article abstract of DOI:10.1248/cpb.46.1522

Photoreaction of arenecarbothioamides (1) with 2-vinylfuran analogues (2, 6) in benzene solution gave tetracyclic indole systems (3, 8) via photogenerated diarylethylene intermediates. In the case of reaction of furan- or thiophenecarbothioamide (1c, 1d) with 2-furanacrylic acid (2-i), 2,3-diaryl-2-pyrrolin-5-ones (5c-i, 5d-i) were obtained.

Full text of DOI:10.1248/cpb.46.1522

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