Aldonitrones as aldehyde surrogates in solvent free synthesis of chalcones under mechanochemical activation

Jesna Antony; John P. Rappai; Kala Ramakrishnan; Rakesh Natarajan

Results in Chemistry (Jan 2021)

Aldonitrones as aldehyde surrogates in solvent free synthesis of chalcones under mechanochemical activation

Jesna Antony,
John P. Rappai,
Kala Ramakrishnan,
Rakesh Natarajan

Affiliations

Jesna Antony: Department of Applied Chemistry, Cochin University of Science and Technology, Kochi 22, India
John P. Rappai: Department of Chemistry, Government Victoria College, Palakkad 678001, India
Kala Ramakrishnan: Department of Applied Chemistry, Cochin University of Science and Technology, Kochi 22, India; Corresponding authors.
Rakesh Natarajan: Department of Applied Chemistry, Cochin University of Science and Technology, Kochi 22, India; Corresponding authors.

Journal volume & issue: Vol. 3
p. 100224

Abstract

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Nitrones perform as aldehyde surrogates in the preparation of chalcones via mechanochemical activation under solvent free condition. Aldonitrones containing electron releasing and electron withdrawing substituent on the C-aryl group exhibit differential reactivity in this reaction.

Published in Results in Chemistry

ISSN: 2211-7156 (Online)
Publisher: Elsevier
Country of publisher: Netherlands
LCC subjects: Science: Chemistry
Website: https://www.journals.elsevier.com/results-in-chemistry/

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