Efficient synthesis of highly substituted pyrroles based on the tandem reactions: intermolecular amination and Pd(II)-catalyzed intramolecular hydroamidation
摘要:
A novel and efficient method for construction of polysubstituted pyrroles, which included an intermolecular amination and Pd(II)-catalyzed intramolecular hydroamidation, was developed. It was found that the reactions gave high yields (55-92%). Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
Bi(III)-Catalyzed Intermolecular Reactions of (<i>Z</i>)-Pent-2-en-4-yl Acetates with Ethynylarenes for the Construction of Multisubstituted Fluorene Skeletons through a Cascade Electrophilic Addition/Cycloisomerization Sequence
A Bi(III)-catalyzed method for the synthesis of highly conjugated aromatic multisubstituted fluorene with (Z)-pent-2-en-4-yl acetates and ethynylarenes via domino reaction is described. In this process, the reaction appears to be very general and suitable for a variety of multisubstituted fluorene.
Efficient synthesis of highly substituted pyrroles based on the tandem reactions: intermolecular amination and Pd(II)-catalyzed intramolecular hydroamidation
A novel and efficient method for construction of polysubstituted pyrroles, which included an intermolecular amination and Pd(II)-catalyzed intramolecular hydroamidation, was developed. It was found that the reactions gave high yields (55-92%). Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
Synthesis of Tetrasubstituted Cyclopentadienes via Palladium-Catalyzed Reaction of (<i>Z</i>)-2-En-4-yn Acetates and <i>N</i>-Methyl Indoles
An efficient approach for the synthesis of tetrasubstituted cyclopentadienes through Pd-catalyzed reactions of (Z)-2-en-4-yn acetates with substituted indoles was developed. This methodology has the advantages of broad scope, simple conditions and easily accessible starting materials.