ChemInform Abstract: Lithiated Azafulvenes by Halogen/Metal Interchange of Brominated 6-(Diisopropylamino)-1-azafulvene Derivatives. Novel Synthesis of 5-Mono- and 4,5-Disubstituted 1H-Pyrrole-2-carbaldehydes
Autor: | Petr Hess, Joseph M. Muchowski, Markus E. Scheller, Brian L. Bray |
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Rok vydání: | 1989 |
Předmět: | |
Zdroj: | ChemInform. 20 |
ISSN: | 0931-7597 |
DOI: | 10.1002/chin.198911152 |
Popis: | The first known lithiated 1-azafulvene derivatives were generated by low-temperature halogen/metal interchange, with t-BuLi, from the corresponding brominated 6-diisopropylamino compounds 3b and 12. These Li species reacted with sundry eletrophilic reagents to give products which, on basic hydrolysis, were converted into 5-mono- or 4,5-disubstituted pyrrole-2-carbaldehydes 10 and 16, respectively. |
Databáze: | OpenAIRE |
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