Tetrahydropyridinium bromide: Useful synthon to functionalized pyrrolidines
Autor: | Fabio Ponticelli, Rossella Noschese, Luca Guideri |
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Rok vydání: | 2011 |
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Zdroj: | Journal of Heterocyclic Chemistry. 49:297-302 |
ISSN: | 0022-152X |
DOI: | 10.1002/jhet.823 |
Popis: | 1-benzyl-5-(ethoxycarbonyl)-2,3,4,5-tetrahydropyridinium bromide undergoes ring contraction with a series of nucleophiles, getting 2,2-disubstitued pyrrolidines. Moreover, from some of the new 2,2-disubstitued pyrrolidines were synthesized spiro-pyrrolidines. J. Heterocyclic Chem.,(2011). |
Databáze: | OpenAIRE |
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