The unexpected influence of aryl substituents in n-aryl-3-oxobutanamides on the behavior of their multicomponent reactions with 5-amino-3-methylisoxazole and salicylaldehyde

19Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

The switchable three-component reactions of 5-amino-3-methylisoxazole, salicylaldehyde and N - aryl-3-oxobutanamides under different conditions were studied and discussed. The unexpected influence of the aryl substituent in N- aryl-3-oxobutanamides on the behavior of the reaction was discovered. The key influence of ultrasonication and Lewis acid catalysts led to an established protocol to selectively obtain two or three types of heterocyclic scaffolds depending on the substituent in the N-aryl moiety.

Cite

CITATION STYLE

APA

Tkachenko, V. V., Muravyova, E. A., Desenko, S. M., Shishkin, O. V., Shishkina, S. V., Sysoiev, D. O., … Chebanov, V. A. (2014). The unexpected influence of aryl substituents in n-aryl-3-oxobutanamides on the behavior of their multicomponent reactions with 5-amino-3-methylisoxazole and salicylaldehyde. Beilstein Journal of Organic Chemistry, 10, 3019–3030. https://doi.org/10.3762/bjoc.10.320

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free