Photochemical Aryl Radical Cyclizations to Give (E)-3-Ylideneoxindoles
(E)-3-Ylideneoxindoles are prepared in methanol in reasonable to good yields, as adducts of photochemical 5-exo-trig of aryl radicals, in contrast to previously reported analogous radical cyclizations initiated by tris(trimethylsilyl)silane and azo-initiators that gave reduced oxindole adducts.
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI AG
2014-09-01
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| Serier: | Molecules |
| Fag: | |
| Online adgang: | http://www.mdpi.com/1420-3049/19/10/15891 |
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