Over-Oxidation as the Key Step in the Mechanism of the MoCl5 -Mediated Dehydrogenative Coupling of Arenes-Reference-Cited by-同舟云学术

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Over-Oxidation as the Key Step in the Mechanism of the MoCl5 -Mediated Dehydrogenative Coupling of Arenes

Published:2015-10-16 Issue:3 Volume:55 Page:1156-1159
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Schubert Moritz¹,Franzmann Peter¹,Wünsche von Leupoldt Anica²,Koszinowski Konrad³,Heinze Katja²,Waldvogel Siegfried R.¹

Affiliation:

1. Department of Organic Chemistry; Johannes Gutenberg University Mainz; Duesbergweg 10-14 55128 Mainz Germany

2. Department of Inorganic and Analytical Chemistry; Johannes Gutenberg University Mainz, Duesbergweg 10-14; 55128 Mainz Germany

3. Institute of Organic and Biomolecular Chemistry; Georg-August-Universität Göttingen; Tammannstrasse 2 37077 Göttingen Germany

Funder

Center of Innovative and Emerging Materials (CINEMA)

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference62 articles.

1. Comparison of Oxidative Aromatic Coupling and the Scholl Reaction

2. Oxidative aromatische Kupplung und Scholl-Reaktion im Vergleich

3. Oxidative transformation of aryls using molybdenum pentachloride

4. Oxidative Coupling Reactions Mediated by MoCl5 Leading to 2,2′-Cyclolignans: The Specific Role of HCl

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5. The Scholl Reaction as a Powerful Tool for Synthesis of Curved Polycyclic Aromatics;Chemical Reviews;2022-08-12

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