Nitrones and nucleobase-containing spiro-isoxazolidines derived from isatin and indanone: solvent-free microwave-assisted stereoselective synthesis and theoretical calculations-Reference-Cited by-同舟云学术

Nitrones and nucleobase-containing spiro-isoxazolidines derived from isatin and indanone: solvent-free microwave-assisted stereoselective synthesis and theoretical calculations

Published:2017 Issue:77 Volume:7 Page:48980-48988
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Maiuolo Loredana¹²³⁴^ORCID,Merino Pedro⁵⁶⁷⁸^ORCID,Algieri Vincenzo¹²³⁴^ORCID,Nardi Monica¹²³⁴⁹^ORCID,Di Gioia Maria Luisa¹⁰²³⁴^ORCID,Russo Beatrice¹²³⁴^ORCID,Delso Ignacio¹¹¹²⁶⁷⁸,Tallarida Matteo Antonio¹²³⁴^ORCID,De Nino Antonio¹²³⁴^ORCID

Affiliation:

1. Dipartimento di Chimica e Tecnologie Chimiche

2. Università della Calabria

3. 87036 Rende

4. Italy

5. Institute of Biocomputation and Physics of Complex Systems (BIFI)

6. Universidad de Zaragoza-CSIC

7. 50009 Zaragoza

8. Spain

9. Dipartimento di Agraria

10. Dipartimento di Farmacia e Scienze della Salute e della Nutrizione

11. Servicio de Resonancia Magnética Nuclear

12. CEQMA

Abstract

Here, we present a highly efficient approach to nucleobase-containing spiro-isoxazolidines with potential biological activity starting from isatinyl/indanyl nitrones.

Funder

University of Calabria

Ministerio de Ciencia e Innovación

University of Zaragoza

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA09995A

Reference40 articles.

1. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents