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Photochemical Formation of Indanylpyrrole Derivatives from 2,2′-(o-Phenylenedivinylene)dipyrrole
✍ Scribed by Nikola Basarić; Slavica Tomšić; Željko Marinić; Marija Šindler-Kulyk
- Book ID
- 104202533
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 132 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
Photochemically induced intra-and inter-molecular reaction of 2,2 H -(1,2-phenylenedivinylene)dipyrrole (4a) led to a mixture of geometric isomers of 5 8) in 40% yield. The compounds were isolated and characterized spectroscopically and by catalytic hydrogenation to 5 7) were isolated in addition to 8. Under the same conditions N,N H -dimethyl-2,2 H -(1,2-phenylenedivinylene) dipyrrole (4b) undergoes only cis-trans-isomerization.
📜 SIMILAR VOLUMES
New photochemically induced intramolecular cycloaddition and double cycloaddition of 5,5%-dimethyl-2,2%-(ophenylenedivinylene)dipyrrole (4b) led to the formation of 2-{[2-(5-methyl-2-pyrrolyl)indan-1-ylidene]methinyl}-5-methylpyrrole (8) and 2-methyl-9-(5-methyl-2-pyrrolyl)-3b,4,8b,9-tetrahydro-4,5-