Reinventing the De Mayo reaction: synthesis of 1,5-diketones or 1,5-ketoesters via visible light [2+2] cycloaddition of β-diketones or β-ketoesters with styrenes-Reference-Cited by-同舟云学术

Reinventing the De Mayo reaction: synthesis of 1,5-diketones or 1,5-ketoesters via visible light [2+2] cycloaddition of β-diketones or β-ketoesters with styrenes

Published:2018 Issue:82 Volume:54 Page:11602-11605
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Martinez-Haya Rebeca¹²³⁴^ORCID,Marzo Leyre⁵⁶⁷⁸^ORCID,König Burkhard⁵⁶⁷⁸^ORCID

Affiliation:

1. Instituto de Tecnología Química

2. Universitat Politècnica de València-Consejo Superior de Investigaciones Científicas

3. Valencia

4. Spain

5. Universität Regensburg

6. Fakultät für Chemie und Pharmazie

7. 93040 Regensburg

8. Germany

Abstract

Taking a different route yields the same product of the De Mayo reaction, but allows the use of visible light instead of UV irradiation.

Funder

Deutscher Akademischer Austauschdienst

Alexander von Humboldt-Stiftung

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC07044J

Reference59 articles.

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2. New synthetic approaches to fused-ring carbocycles based on intramolecular photocycloadditions of 1,3-dione enol esters

3. The intramolecular [2 + 2] photoaddition/cyclobutane-fragmentation sequence in organic synthesis

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