Issue 63, 2020, Issue in Progress

Vilsmeier reagent, NaHSe and diclofenac acid chloride: one-pot synthesis of a novel selenoindolinone with potent anticancer activity

Abstract

An effective and straightforward synthesis of 3-seleno functionalized indolinone (5) involving Vilsmeier reagent is presented. Likewise, a procedure to achieve lactamization of diclofenac with excellent yields by using hydrides is also ascertained. Compound 5 exhibited impressive growth inhibition in most of the cell lines in an NCI-60 panel, particularly towards resistant breast cancer cells.

Graphical abstract: Vilsmeier reagent, NaHSe and diclofenac acid chloride: one-pot synthesis of a novel selenoindolinone with potent anticancer activity

Supplementary files

Article information

Article type
Paper
Submitted
26 Aug 2020
Accepted
12 Oct 2020
First published
19 Oct 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 38404-38408

Vilsmeier reagent, NaHSe and diclofenac acid chloride: one-pot synthesis of a novel selenoindolinone with potent anticancer activity

A. C. Ruberte, C. Aydillo, A. K. Sharma, C. Sanmartín and D. Plano, RSC Adv., 2020, 10, 38404 DOI: 10.1039/D0RA07332F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements