Enantioselective [4+4] photodimerization of anthracene-2,6-dicarboxylic acid mediated by a C2-symmetric chiral template-Reference-Cited by-同舟云学术

Enantioselective [4+4] photodimerization of anthracene-2,6-dicarboxylic acid mediated by a C2-symmetric chiral template

Published:2016 Issue:5 Volume:52 Page:1032-1035
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Maturi Mark M.¹²³⁴,Fukuhara Gaku⁵⁶⁷⁸,Tanaka Koichiro⁵⁶⁷⁸,Kawanami Yuko⁵⁶⁷⁸,Mori Tadashi⁵⁶⁷⁸,Inoue Yoshihisa⁵⁶⁷⁸,Bach Thorsten¹²³⁴

Affiliation:

1. Department Chemie and Catalysis Research Center (CRC)

2. Technische Universität München

3. 85747 Garching

4. Germany

5. Department of Applied Chemistry

6. Osaka University

7. Suita 565-0871

8. Japan

Abstract

A chiral template was shown to bind the title compound by hydrogen bonding resulting in enantioselectivities of up to 55% enantiomeric excess (ee) in the [4+4] anthracene photodimerization.

Funder

Deutsche Forschungsgemeinschaft

Alexander von Humboldt-Stiftung

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/2016/CC/C5CC09107A

Reference41 articles.

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3. Optical switches with biplanemers obtained by intramolecular photocycloaddition reactions of tethered arenes

4. Theoretical and Experimental Investigations of Circular Dichroism and Absolute Configuration Determination of Chiral Anthracene Photodimers

5. Absolute configuration determination of theanti-head-to-head photocyclodimer of anthracene-2-carboxylic acid through cocrystallization withL-prolinol

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