Synthesis of azahelicenes through Mallory reaction of imine precursors: corannulene substrates provide an exception to the rule in oxidative photocyclizations of diarylethenes-Reference-Cited by-同舟云学术

Synthesis of azahelicenes through Mallory reaction of imine precursors: corannulene substrates provide an exception to the rule in oxidative photocyclizations of diarylethenes

Published:2021 Issue:11 Volume:12 Page:3977-3983
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Ghosh Animesh¹²³⁴⁵,Csókás Dániel⁶⁷⁸⁹^ORCID,Budanović Maja¹²³⁴⁵,Webster Richard D.¹²³⁴⁵^ORCID,Pápai Imre⁶⁷⁸⁹^ORCID,Stuparu Mihaiela C.¹²³⁴⁵^ORCID

Affiliation:

1. Division of Chemistry and Biological Chemistry

2. School of Physical and Mathematical Sciences

3. Nanyang Technological University

4. Singapore

5. 637371 Singapore

6. Institute of Organic Chemistry

7. Research Centre for Natural Sciences

8. H-1117 Budapest

9. Hungary

Abstract

First azahelicene synthesis from corannulene-based imine precursors is presented.

Funder

Nanyang Technological University

Ministry of Education - Singapore

Agency for Science, Technology and Research

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/SC/D0SC06730J

Reference64 articles.

1. F. B. Mallory and C. W.Mallory , Photocyclization of Stilbenes and Related Molecules , in Organic Reactions , Wiley , New York , 1984 , vol. 30

2. Photochemical Reactions as Key Steps in Organic Synthesis

3. Photochemical Oxidative Cyclisation of Stilbenes and Stilbenoids—The Mallory-Reaction

4. Switching the Mallory Reaction to Synthesis of Naphthalenes, Benzannulated Heterocycles, and Their Derivatives

5. Photochemical Conversion of Stilbene to Phenanthrene

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