A convergent one-pot construction of disubtituted pyrrolidine and piperidine framworks throug a simple protocol involving intramolecular conjugated addition of a nitrogen nucleophile to an electrophile olefin followed by intramolecular trapping of the generated enolated by a built-in unsaturated acceptor
Tandem Michael reactions for the construction of pyrrolidine and piperidine ring systems.
BENETTI, Simonetta;
1990
Abstract
A convergent one-pot construction of disubtituted pyrrolidine and piperidine framworks throug a simple protocol involving intramolecular conjugated addition of a nitrogen nucleophile to an electrophile olefin followed by intramolecular trapping of the generated enolated by a built-in unsaturated acceptorFile in questo prodotto:
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