Rh(III)‐Catalyzed C‐2 Alkylation of Indoles followed by a Post‐Synthetic Modification via the Ugi Reaction
Abstract Indole derivatives substituted at the C‐2 position have shown important biological activities. Due to these properties, several methods have been described for the preparation of structurally diverse indoles. In this work, we have synthesized highly functionalized indole derivatives via Rh(...
Main Authors: | Marcelo Augusto Pereira Januário, Demetrius P. deSouza, Prof. Dr. Julio Zukerman‐Schpector, Prof. Dr. Arlene G. Corrêa |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley-VCH
2023-06-01
|
Series: | ChemistryOpen |
Subjects: | |
Online Access: | https://doi.org/10.1002/open.202300070 |
Similar Items
-
Improved Method for Preparation of 3-(1<i>H</i>-Indol-3-yl)benzofuran-2(3<i>H</i>)-ones
by: Igor Yu. Grishin, et al.
Published: (2022-03-01) -
Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines
by: Amit Kumar, et al.
Published: (2013-10-01) -
Recent developments in copper-catalyzed radical alkylations of electron-rich π-systems
by: Kirk W. Shimkin, et al.
Published: (2015-11-01) -
Synthesis of quinoline-3-carboxylates by a Rh(II)-catalyzed cyclopropanation-ring expansion reaction of indoles with halodiazoacetates
by: Magnus Mortén, et al.
Published: (2015-10-01) -
Gold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolones
by: Xiaochen Du, et al.
Published: (2018-10-01)