@article{19582b1688104f10b1c3ad948450e287,
title = "Concise synthesis of new bridged-nicotine analogues",
abstract = "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.",
keywords = "Former Faculty of Pharmaceutical Sciences",
author = "Fran{\c c}ois Crestey and Geert Hooyberghs and Kristensen, {Jesper Langgaard}",
note = "Keywords: Pyridine metallation; Bridged-nicotine analogue; Suzukie-Miyaura cross-coupling reaction; Nicotinic acetylcholine receptor; Intramolecular reductive amination",
year = "2012",
month = feb,
day = "4",
doi = "10.1016/j.tet.2011.12.029",
language = "English",
volume = "68",
pages = "1417--1421",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Pergamon Press",
number = "5",
}