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Chlorophyll Triggered One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones via Photo Induced Electron transfer reaction

Harsh, Simran; Kumar, Sanjay; Sharma, Rohit; Kumar, Yogesh; Kumar, Rupesh

Chlorophyll Triggered One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones via Photo Induced Electron transfer reaction Thumbnail


Authors

Simran Harsh

Sanjay Kumar

Rohit Sharma

Yogesh Kumar

Rupesh Kumar



Abstract

The photocatalytic potential of chlorophyll has been investigated for the facile synthesis of dihydropyrimidinones utilizing concentrated solar irradiation towards sustainable energy solutions. This, one-pot, multicomponent Biginelli reaction, which involves a photoinduced electron transfer (PET) mechanism, affords a green and efficient approach for the transformation of the commercial aldehydes, β-keto ester and urea into valuable 3,4-dihydropyrimidin-2(1H)-ones with wide substrate scope and diversity. These improved reaction conditions allow the formation of a variety of substituted dihydropyrimidinones with high yields and purity in a short duration of time and mild reaction conditions.

Citation

Harsh, S., Kumar, S., Sharma, R., Kumar, Y., & Kumar, R. (2020). Chlorophyll Triggered One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones via Photo Induced Electron transfer reaction. Arabian Journal of Chemistry, 13(3), 4720-4730. https://doi.org/10.1016/j.arabjc.2019.11.002

Journal Article Type Article
Acceptance Date Nov 10, 2019
Online Publication Date Nov 22, 2019
Publication Date 2020-03
Deposit Date Nov 22, 2019
Publicly Available Date Jul 5, 2020
Journal Arabian Journal of Chemistry
Print ISSN 1878-5352
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 13
Issue 3
Pages 4720-4730
DOI https://doi.org/10.1016/j.arabjc.2019.11.002
Public URL https://durham-repository.worktribe.com/output/1282777

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Publisher Licence URL
http://creativecommons.org/licenses/by-nc-nd/4.0/

Copyright Statement
© 2019 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).





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