Indium-mediated allenylation of arylacyl bromides in a route for the synthesis of substituted furans
摘要:
A three-step, single purification procedure has been developed for the concise synthesis of substituted furans from arylacyl bromides. (C) 2014 Elsevier Ltd. All rights reserved.
The reaction of tributyltinenolates with α-halogenoketones gave substituted furans which were not derived from the normal cross-coupling products, 1,4-diketones, but were formed instead through addition of the tin enolate to the α-halogenoketones.
Direct β-Arylation of Furans with Aryl Iodides Catalyzed by Dinuclear Palladium Complexes
作者:Naofumi Tsukada、Takahiro Goto、Hayate Kato
DOI:10.3987/com-17-13824
日期:——
Dinuclear palladium complexes formed by a chelate-bridging ligand showed beta-selectivity in the direct arylation of furans with iodoarenes. In contrast, the arylation using PPh3, or bpy as ligands gave alpha-arylfurans as major products. The arylation can be applied to several furans bearing functional groups except electron-withdrawing groups.
KOSUGI, MASANORI;TAKANO, IZUMI;HOSHINO, ISAO;MIGITA, TOSHIHIKO, J. CHEM. SOC. CHEM. COMMUN., 1983, N 18, 989-990
A three-step, single purification procedure has been developed for the concise synthesis of substituted furans from arylacyl bromides. (C) 2014 Elsevier Ltd. All rights reserved.