Stereoselective synthesis of spirocyclic pyrrolidines/pyrrolizidines/pyrrolothiazolidines using l-proline functionalized manganese ferrite nanorods as a novel heterogeneous catalyst-Reference-Cited by-同舟云学术

Stereoselective synthesis of spirocyclic pyrrolidines/pyrrolizidines/pyrrolothiazolidines using l-proline functionalized manganese ferrite nanorods as a novel heterogeneous catalyst

Published:2021 Issue:24 Volume:11 Page:14755-14768
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Akhavan Malihe¹²³⁴⁵,Bekhradnia Ahmadreza¹²³⁴⁵^ORCID

Affiliation:

1. Pharmaceutical Sciences Research Centre

2. Department of Medicinal Chemistry

3. Mazandaran University of Medical Sciences

4. Sari

5. Iran

Abstract

An efficient, green, one-pot, and three-component protocol has been reported for the stereoselective synthesis of a new class of spiro thiazolidines.

Funder

National Institute for Medical Research Development

Mazandaran University of Medical Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA00841B

Reference43 articles.

1. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

2. A facile regioselective 1,3-dipolar cycloaddition protocol for the synthesis of new class of quinolinyl dispiro heterocycles

3. Synthesis of novel spiropyrrolizidines as potent antimicrobial agents for human and plant pathogens

4. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

5. Harnessing interrupted Fischer in continuous flow: sustainable synthesis of (spiro)indolenine and (spiro)indoline privileged scaffolds

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