Advanced palladium free approach to the synthesis of substituted alkene oxindoles: Via aluminum-promoted Knoevenagel reaction

13Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

Abstract

A synthetic route for the synthesis of C24, as well as for the design of focused libraries of direct AMPK activators was developed based on a convergent strategy. The proposed scheme corresponds to the current trends in C-H bond functionalization. The use of aluminum isopropoxide for the Knoevenagel condensation of oxindole with benzophenones is a noticeable point of this work.

Cite

CITATION STYLE

APA

Novikova, D. S., Grigoreva, T. A., Zolotarev, A. A., Garabadzhiu, A. V., & Tribulovich, V. G. (2018). Advanced palladium free approach to the synthesis of substituted alkene oxindoles: Via aluminum-promoted Knoevenagel reaction. RSC Advances, 8(60), 34543–34551. https://doi.org/10.1039/c8ra07576j

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