Exploring the Oxidative Cyclization of Substituted N ‐Aryl Enamines: Pd‐Catalyzed Formation of Indoles from Anilines-Reference-Cited by-同舟云学术

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Exploring the Oxidative Cyclization of Substituted N ‐Aryl Enamines: Pd‐Catalyzed Formation of Indoles from Anilines

Published:2011-05-12 Issue:26 Volume:17 Page:7298-7303
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Neumann Julia J.¹,Rakshit Souvik²,Dröge Thomas²,Würtz Sebastian³,Glorius Frank²

Affiliation:

1. Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim am Rhein (Germany)

2. Westfälische Wilhelms‐Universität Münster, Organisch‐Chemisches Institut, Corrensstrasse 40, 48149 Münster (Germany), Fax: (+49) 251‐833‐3202

3. Archimica GmbH, Industriepark Höchst, D569, 65926 Frankfurt am Main (Germany)

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201100631

Reference91 articles.

1. Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases

2. The First Potent Inhibitor of Mammalian Group X Secreted Phospholipase A2: Elucidation of Sites for Enhanced Binding

3. Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro [indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3H-indole-3,2′-thiazolidine]-3′(1,2,4-triazol-3-yl)-2,4′(1H)-dione

4.

5. Novel conducting polymers based on thieno[3,2-b]indoles: Electrochemical properties and molecular structure

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