The Photoaddition of Pyrroles to Arylethenes and Arylethynes
โ Scribed by Austin, Mark ;Covell, Christopher ;Gilbert, Andrew ;Hendrickx, Ramon
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 378 KB
- Volume
- 1997
- Category
- Article
- ISSN
- 0947-3440
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โฆ Synopsis
Abstract
The photochemical reactions of styrene, (E)โstilbene, phenylโethyne, and diphenylethyne with pyrrole and Nโmethylpyrrole have been investigated. The pyrroles quench the fluorescence of the phenylethenes and phenylethynes efficiently and broad structureless emissions attributed to exciplexes are observed from the Nโmethylpyrrole systems. Substituted pyrroles (1:1 and 2:1 adducts) are formed from irradiation of the phenylethenes with pyrrole, and 2โstyrylpyrroles result from the phenylethynes. Styrene, but none of the other arenes, undergoes photoaddition to Nโmethylpyrrole in the presence of 10% acetic acid.
๐ SIMILAR VOLUMES
Thiopyridonc ( I a) and 2-thiopyrimidone (1 bl undcrgo photoaddition to olefins 10 give ?-substituted hetcrocyclcs, probably via rhietanes formed by [ 2 i -21 addition across the C=S bond. A novel two-fold addition of isobutene is discussed.