A simple method for the synthesis of 4-aryl-9-oxynaphthofuranone lignans
K Kobayashi, K Maeda, T Uneda, O Morikawa…
Index: Kobayashi, Kazuhiro; Maeda, Kouji; Uneda, Tomokazu; Morikawa, Osamu; Konishi, Hisatoshi Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 4 p. 443 - 446
Full Text: HTML
Citation Number: 0
Abstract
The 9-aryl-4-oxynaphthofuran-1 (3H)-one system is generally synthesized in two steps from α-aryl-o-toluic acid derivatives. The method involves a tandem conjugate addition– Dieckmann type condensation between α-lithiated α-aryl-o-toluic acid derivatives and 2- furan-2 (5H)-one as a key step followed by simple dehydrogenation or dehydration, and can be applied to the synthesis of two natural lignans (neojusticidin A and neojusticidin B).
Related Articles:
Synthesis and characterization of benzannelated thienyl oligomers
[Amaladass, Pitchamuthu; Clement, J. Arul; Mohanakrishnan, Arasambattu K. European Journal of Organic Chemistry, 2008 , # 22 p. 3798 - 3810]
Efficient Synthesis of 3-Arylphthalides†
[Godbole, Himanshu M.; Joseph, Augustine R. Journal of Chemical Research, Synopses, 1998 , # 6 p. 332 - 333]
Indane??1, 3??dione, phthalimidine and phthalide derivatives as alkylating agents
[Barili, Pier Luigi; Scartoni, Valerio Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 1199 - 1202]