Hydroxyarylketones via Ring-Opening of Lactones with Aryllithium Reagents: An Expedient Synthesis of (±)-Anabasamine
L Miao, SC DiMaggio, ML Trudell
Index: Miao, Lei; Dimaggio, Stassi C.; Trudell, Mark L. Synthesis, 2010 , # 1 p. 91 - 97
Full Text: HTML
Citation Number: 3
Abstract
Abstract The regioselective ring-opening of lactones (δ-valerolactone and γ-butyrolactone) with aryllithium reagents is reported for the construction of a series of δ-hydroxy aryl ketones and γ-hydroxy aryl ketones. Application of this method for the expeditious syntheses of (±)- anabasamine and its nicotine-related analogue are also described.
Related Articles:
[Zidani, Ahmed; Vaultier, Michel Tetrahedron Letters, 1986 , vol. 27, # 7 p. 857 - 860]