Substrate substitution effects in the Fries rearrangement of aryl esters over zeolite catalysts-Reference-Cited by-同舟云学术

Substrate substitution effects in the Fries rearrangement of aryl esters over zeolite catalysts

Published:2020 Issue:13 Volume:10 Page:4282-4292
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Lin Ronghe¹²³⁴⁵,Mitchell Sharon¹²³⁴⁵^ORCID,Netscher Thomas⁶⁷⁸⁵^ORCID,Medlock Jonathan⁶⁷⁸⁵,Stemmler René T.⁶⁷⁸⁵^ORCID,Bonrath Werner⁶⁷⁸⁵,Létinois Ulla⁶⁷⁸⁵,Pérez-Ramírez Javier¹²³⁴⁵^ORCID

Affiliation:

1. Institute for Chemical and Bioengineering

2. Department of Chemistry and Applied Biosciences

3. ETH Zurich

4. Zurich 8093

5. Switzerland

6. DSM Nutritional Products

7. Research and Development

8. Basel 4002

Abstract

The reaction scheme of the Fries rearrangement of aryl esters over zeolite catalysts strongly depends on the framework type, acidic properties, and substrate identity.

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CY/D0CY00590H

Reference38 articles.

1. Über Homologe des Cumaranons und ihre Abkömmlinge

2. USES OF THE FRIES REARRANGEMENT FOR THE PREPARATION OF HYDROXYARYLKETONES. A REVIEW

3. Atropo-Enantioselective Total Synthesis of Knipholone and Related Antiplasmodial Phenylanthraquinones

4. The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics

5. Zeolite-catalyzed rearrangement of phenyl acetate

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