Concise synthesis of new bridged-nicotine analogues

Research output: Contribution to journalJournal articleResearchpeer-review

This study describes a very efficient strategy for the synthesis of two new bridged-nicotine analogues. Starting from either 4- or 3-chloropyridine the desired tricyclic ring systems are accessed in just three steps in 23% and 40% overall yield, respectively.
Original languageEnglish
Issue number5
Pages (from-to)1417-1421
Publication statusPublished - 4 Feb 2012

Bibliographical note

Keywords: Pyridine metallation; Bridged-nicotine analogue; Suzukie-Miyaura cross-coupling reaction; Nicotinic acetylcholine receptor; Intramolecular reductive amination

ID: 37426122