Tetrahydropyridinium bromide: Useful synthon to functionalized pyrrolidines

Autor: Fabio Ponticelli, Rossella Noschese, Luca Guideri
Rok vydání: 2011
Předmět:
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